Human Movement - Akademia Wychowania Fizycznego we Wrocławiu
Transcription
Human Movement - Akademia Wychowania Fizycznego we Wrocławiu
University School of Physical Education in Wrocław University School of Physical Education in Kraków vol. 17, number 1 (March), 2016 University School of Physical Education in Wrocław (Akademia Wychowania Fizycznego we Wrocławiu) University School of Physical Education in Kraków (Akademia Wychowania Fizycznego im. Bronisława Czecha w Krakowie) Human Movement quarterly vol. 17, number 1 (March), 2016, pp. 1– 60 Editor-in-Chief Alicja Rutkowska-Kucharska University School of Physical Education, Wrocław, Poland Associate EditorEdward Mleczko University School of Physical Education, Kraków, Poland Editorial Board Physical activity, fitness and health Wiesław Osiński University School of Physical Education, Poznań, Poland Applied sport sciences Zbigniew Trzaskoma Józef Piłsudski University of Physical Education, Warszawa, Poland Biomechanics and motor control Tadeusz Bober University School of Physical Education, Wrocław, Poland Kornelia Kulig University of Southern California, Los Angeles, USA Physiological aspects of sports Andrzej Suchanowski Józef Rusiecki Olsztyn University College, Olsztyn, Poland Psychological diagnostics of sport and exercise Andrzej Szmajke Opole University, Opole, Poland Advisory Board Wojtek J. Chodzko-Zajko Gudrun Doll-Tepper Józef Drabik Kenneth Hardman Andrew Hills Zofia Ignasiak Slobodan Jaric Han C.G. Kemper Wojciech Lipoński Gabriel Łasiński Robert M. Malina Melinda M. Manore Philip E. Martin Joachim Mester Toshio Moritani Andrzej Pawłucki John S. Raglin Roland Renson Tadeusz Rychlewski James F. Sallis James S. Skinner Jerry R. Thomas Karl Weber Peter Weinberg Marek Woźniewski Guang Yue Wladimir M. Zatsiorsky Jerzy Żołądź University of Illinois, Urbana, Illinois, USA Free University, Berlin, Germany University School of Physical Education and Sport, Gdańsk, Poland University of Worcester, Worcester, United Kingdom Queensland University of Technology, Queensland, Australia University School of Physical Education, Wrocław, Poland University of Delaware, Newark, Delaware, USA Vrije University, Amsterdam, The Netherlands University School of Physical Education, Poznań, Poland University School of Physical Education, Wrocław, Poland University of Texas, Austin, Texas, USA Oregon State University, Corvallis, Oregon, USA Iowa State University, Ames, Iowa, USA German Sport University, Cologne, Germany Kyoto University, Kyoto, Japan University School of Physical Education, Wrocław, Poland Indiana University, Bloomington, Indiana, USA Catholic University, Leuven, Belgium University School of Physical Education, Poznań, Poland San Diego State University, San Diego, California, USA Indiana University, Bloomington, Indiana, USA University of North Texas, Denton, Texas, USA German Sport University, Cologne, Germany Hamburg, Germany University School of Physical Education, Wrocław, Poland Cleveland Clinic Foundation, Cleveland, Ohio, USA Pennsylvania State University, State College, Pennsylvania, USA University School of Physical Education, Kraków, Poland Translation: Agnieszka Piasecka Design: Agnieszka Nyklasz Copy editor: Beata Irzykowska Statistical editor: Małgorzata Kołodziej Indexed in: SPORTDiscus, Index Copernicus, Altis, Sponet, Scopus, CAB Abstracts, Global Health 14 pkt wg rankingu Ministerstwa Nauki i Szkolnictwa Wyższego © Copyright 2016 by Wydawnictwo AWF we Wrocławiu ISSN 1732-3991 http://156.17.111.99/hum_mov Editorial Office Dominika Niedźwiedź 51-612 Wrocław, al. Ignacego Jana Paderewskiego 35, Poland, tel. 48 71 347 30 51, hum_mov@awf.wroc.pl This is to certify the conformity with PN-EN-ISO 9001:2009 Circulation: 100 HUMAN MOVEMENT 2016, vol. 17 (1) contents ph y sic a l ac t i v i t y, f i t n e s s a n d h e a lt h Ben D. Dickinson, Michael J. Duncan, Emma L.J. Eyre Exercise and academic achievement in children: effects of acute class-based circuit training........................... 4 Jerzy Eksterowicz, Marek Napierała, Walery Żukow How the Kenyan runner’s body structure affects sports results........................................................................... 8 applied sport science Jennifer Wilson, John Kiely The multi-functional foot in athletic movement: extraordinary feats by our extraordinary feet....................15 Janusz Jaworski, Michał Żak Identification of determinants of sports skill level in badminton players using the multiple regression model......................................................................................................................21 Alicja Rutkowska-Kucharska, Karolina Wuchowicz Body stability and support scull kinematic in synchronized swimming........................................................... 29 biomechanics and motor control Rodrigo Rico Bini, Patria Hume A comparison of static and dynamic measures of lower limb joint angles in cycling: application to bicycle fitting................................................................................................................................. 36 Matthew R. Rhea, Joseph G. Kenn, Mark D. Peterson, Drew Massey, Roberto Simão, Pedro J. Marin, Mike Favero, Diogo Cardozo, Darren Krein Joint-angle specific strength adaptations influence improvements in power in highly trained athletes..........43 Marcelo de Lima Sant’Anna, Gustavo Casimiro-Lopes, Gabriel Boaventura, Sergio Tadeu Farinha Marques, Martha Meriwether Sorenson, Roberto Simão, Verônica Salerno Pinto Anaerobic exercise affects the saliva antioxidant/oxidant balance in high-performance pentathlon athletes.................................................................................................................................................50 Publishing guidelines – Regulamin publikowania prac.......................................................................................... 56 3 HUMAN MOVEMENT 2016, vol. 17 (1), 4– 7 Exercise and academic achievement in children: Effects of acute class-based circuit training doi: 10.1515/humo-2016-0007 Ben D. Dickinson 1 *, Michael J. Duncan 2 , Emma L.J. Eyre 2 1 2 University of Central Lancashire, Preston, United Kingdom Centre for Applied Biological and Exercise Science, Coventry University, Coventry, United Kingdom Abstract Purpose. For schools, the increasingly imposed requirement to achieve well in academic tests puts increasing emphasis on improving academic achievement. While treadmill exercise has been shown to have beneficial effects on cognitive function and cycling ergometers produce stronger effect sizes than treadmill running, it is impractical for schools to use these on a whole-class basis. There is a need to examine if more ecologically valid modes of exercise might have a similar impact on academic achievement. Circuit training is one such modality shown to benefit cognitive function and recall ability and is easily operationalised within schools. Methods. In a repeated measures design, twenty-six children (17 boys, 8 girls) aged 10–11 years (mean age 10.3; SD ± 0.46 years) completed the Wide Range Achievement Test (WRAT 4) at rest and following 30 minutes of exercise. Results. Standardised scores for word reading were significantly higher post exercise (F(1,18) = 49.9, p = 0.0001) compared to rest. In contrast, standardised scores for sentence comprehension (F(1,18) = 0.078, p = 0.783), spelling (F(1,18) = 4.07, p = 0.06) mathematics (F(1,18) = 1.257, p = 0.277), and reading (F(1,18) = 2.09, p = 0.165) were not significantly different between rest and exercise conditions. Conclusions. The results of the current study suggest acute bouts of circuit based exercise enhances word reading but not other areas of academic ability in 10–11 year old children. These findings support prior research that indicates acute bouts of exercise can selectively improve cognition in children. Key words: acute exercise, academic achievement, children Introduction Physical activity and physical education within schools is comprehensively researched and the health benefits of exercise for cardiovascular fitness and general health is widely acknowledged. Research has shown acute exercise to have beneficial effects on cognition and subsequently academic achievement. It has been suggested that children gain cognitive benefits from physical activity [1, 2] with greatest improvements seen in complex mental processing [3]. Standardised achievement in maths and reading [4] as well as increased performance in core academic classes has been reported for children who participate in vigorous physical activity outside of school [5]. For schools the increasingly imposed requirement to achieve well in academic tests puts more emphasis on methods of improving academic achievement. These increased demands place an importance on academic testing and as a result, many schools have responded with a decrease in time dedicated to non-academic subjects [4]. From this perspective, participation in moderate activity of boys and girls aged 2 to 14 has since fallen between 2008 and 2014 [6]. Minutes spent taking part in PE has also fallen [7]. Within schools, children generally engage with wholeclass physical education and so it is important to review the exercise modality used in studies of this nature. Treadmill exercise has been shown to have beneficial * Corresponding author. 4 effects on cognitive function [8], while cycling ergometer use produced stronger effect sizes than treadmill running [9]. This study argued that cycling uses less metabolic energy compared with running and that running resulted in greater ‘neural interference’ and more cognitive demands for movement. Duncan and Johnson [10] also used cycle ergometer training at differing intensities and found that spelling and reading were improved, arithmetic impaired and sentence comprehension unaffected. While the potential for acute exercise to enhance academic achievement is attractive for educational practitioners/teachers, it is impractical for schools to use cycle ergometers or treadmills on a whole class basis. Thus, there is a need to examine whether different, more ecologically valid modes of exercise might have a similar impact on academic achievement. Immediate recall scores were higher following submaximal intensity lessons involving both team games and aerobic training. This can be attributed to exerciseinduced increases in physiological arousal and the cognitive activation induced by the exercise demands. Circuit training is one such modality which has shown benefit cognitive function and recall ability [11] and is easily operationalised in the school setting. No studies appear to have examined whether the changes seen in the aforementioned laboratory studies [8–10] can translate to the school setting in a practical way. The current study sought to address this gap by examining the effects of class-based exercise on preadolescent academic performance. HUMAN MOVEMENT B.D. Dickinson, M.J. Duncan, E.L.J. Eyre, Exercise and academic achievement in children Material and methods Participants Twenty-six children (17 boys, 8 girls) aged 10–11 years (mean age 10.3; SD ± 0.46 years) from the town of Warrington, UK, participated in the study following institutional ethics approval and informed parent and child and school consent. A pre-exercise Physical Activity Readiness Questionnaire was also used to confirm that the children did not have any pre-existing condition that would be exacerbated by physical exercise. None of the children included in the study had a recognised special educational need (e.g. dyslexia) or behavioural problem and nor were they classified as ‘gifted and talented’ according to school records. Children were all drawn from one school representing an area in the mid-range of socio-economic status within the town. Children were not given any inducement to participate and were recruited voluntarily following a presentation given by the researchers to children and parents attending the school concerned. Procedures This study employed repeated measures design whereby participants completed an academic test, comprising measures of reading, spelling, arithmetic and sentence comprehension, as a control result. This was followed 1 week later by a 30-minute circuit style class exercise session followed by a re-sit of the academic test. Both sessions occurred on the same weekday and time of day one week apart. Firstly, to establish baseline academic performance, the Wide Ranging Achievement Task [12] was administered. WRAT 4 is the updated version of the academic achievement test employed by Hillman et al. [8] and in addition to measures of word reading, spelling and arithmetic, now includes an assessment of sentence comprehension. Word reading is a measure of the number of words correctly pronounced aloud and spelling is a measure of the number of words correctly spelt. The reading test comprised 55 words ranging from threeletter words such as ‘see’ and ‘red’, to more complex words such as ‘ubiquitous’ and ‘regicidal’ with children asked to read these aloud to the tester. In the spelling test, children read a series of 42 words in isolation and then in context (e.g. ‘go. The children want to go home’) and asked to spell these words in written form. The words range from two-letter (e.g. ‘go’) to nine-letter (e.g. ‘assiduous’) words. The arithmetic score is a measure of the number of mathematical problems correctly solved. In the assessment of sentence comprehension children were asked to provide the missing word in a given sentence e.g. ‘Dee is having a birthday party for her brother. He will be seven ___ old’ to measure the ability to comprehend information contained in a sentence. This paper and pencil assessment was administrated in silence in the children’s normal classroom and lasted approximately 20 minutes. The WRAT was also administered in the order prescribed by the test guidelines, i.e. (1) word and letter reading, (2) sentence comprehension, (3) spelling and (4) math computation. A within-subjects repeated measures design was employed whereby, one week after the initial WRAT4 test, the children participated in 30 minutes of class-based circuit training. Participants’ heights (cm) and body masses (kg) were assessed using a Seca Stadiometre and weighing scales (Seca Instruments, Frankfurt, Germany). Heart rate monitors were used to measure the intensity of the session for 6 students selected at random and are accepted as a valid measure of assessment of intensity and have demonstrated reliability in test-retest studies [13]. The Polar RS400 (Polar Electro, Kuopio, Finland) were used in the instance. Resting heart rate was recorded for all participants after a 5-minute rest period in a supine position. A 30-minute circuit-based exercise session was conducted with a full school class and consisted of exercise stations of requiring 30 seconds exercising followed by 30 seconds rest. The children were instructed to complete as many repetitions of the selected body-weight based exercises as they could during the 30 seconds. The exercises selected were body weight focused, compound, whole body exercises, chosen as the children were familiar with the exercises from previous PE lessons and designed to use large muscle groups. The circuit stations were Star Jumps, Squat Thrusts, Burpees, Speed Bounces, Modified press ups, Tuck jumps, 5 m shuttle runs, ‘Mountain Climbers’, press ups, sit ups, body weight squats, Bean Bag raises and Stork balance. In order to establish exercise intensity post testing, heart rate was recorded every 5 minutes immediately after an exercise interval on a station. On completion of the exercise session, the children repeated the full WRAT test procedure. The blue and green WRAT4 forms, considered to be equivalent versions, were administered as part of the experimental design to eliminate the potential for practice effects [12]. Statistical analysis For the purpose of analysis, standardised scores on WRAT 4 were employed. Data was screened for normality (Shapiro–Wilk, p > 0.05) and met the assumption. A repeated measures MANOVA was then employed to examine any differences in components of the WRAT, post control and post exercise conditions, wherein the independent variable was time (control vs. exercise) and the dependent variables were standardised WRAT scores for mathematics, reading, spelling, and sentence comprehension. Gender was used as a between subjects factor. Partial eta squared (P 2) was also used as a measure of effect size. The Statistical Package for So5 HUMAN MOVEMENT B.D. Dickinson, M.J. Duncan, E.L.J. Eyre, Exercise and academic achievement in children cial Sciences (SPSS, Version 20, Chicago, Il, USA) was used for all analyses. Results There was a significant multivariate effect for the intervention condition, F(4,15) = 5.54, p = 0.006, Wilks’ Lambda = 0.403, p2 = 0.597. Gender was not significant (p > 0.05) in any of the analyses and is therefore not discussed further. Analysis of each individual dependent variable, with Bonferroni correction, indicated that standardised scores for word reading were significantly higher post exercise (F(1,18) = 49.9, p = 0.0001, p2 = 0.735) compared to control. In contrast, standardised scores for sentence comprehension (F(1,18) = 0.078, p = 0.783, p2 = 0.004), spelling (F(1,18) = 4.07, p = 0.06, p2 = 0.185), mathematics (F(1,18) = 1.257, p = 0.277, p2 = 0.065), and reading (F(1,18) = 2.09, p = 0.165, p2 = 0.104) were not significantly different in control and exercise conditions. Mean ± SD of standardised WRAT scores in control and exercise conditions are shown in Figure 1. Discussion The present study investigated the effect of an acute bout of exercise (30 minutes of circuit based exercise) compared to rest on academic performance (WRAT 4). The findings of the present study, that only word reading scores were significantly different between rest and exercise, matches similar studies using the WRAT test exercise that found improved reading comprehension but not spelling or arithmetic [8] or improved spelling and reading scores [10]. These positive benefits could be attributed to the cognitive benefits resulting from physical activity [1, 2] particularly immediate and delayed recall [11]. The results also support those of [8, 10] in that acute bouts of class based exercise have an adverse effect on arithmetic. The findings of the current study could also be interpreted in another way. The Word reading test is the first Figure 1. Mean ± SD of standardised WRAT scores in control and exercise conditions (*p = 0.001) 6 in the WRAT schedule and will occur within 20 minutes of the cessation of the exercise bout. The significance of results in only this test may be attributed to acute exercise-induced increases in memory storage and physiological arousal leading to temporary cognitive activation that are possibly time limited. This would be supported by higher immediate recall scores following submaximal intensity lessons involving both team games and aerobic training. If this were the case, however, increased scores should be realistically expected for all the tests. It is certainly important to acknowledge that the order of testing required in the WRAT battery may indirectly affect the findings of studies with prolonged testing batteries post exercise and would be an area for further clarification in studies of this nature. Future alterations to the order of administration of the WRAT are limited by the test procedure itself. The order of administration of the tests in the present study followed guidance on use of the WRAT [12] and the way prior studies using this test have employed it [8, 10]. Firstly, Word Reading was administered, then Sentence Comprehension, Spelling and lastly Math Computation. There is the option for the four subtests to be given separately or in combination of two or more at one sitting; however, they emphasize the Word Reading subtest should be given before the Sentence Completion subtest. Thus, in the context of the current procedure, it may be that the temporal effects of the bout of exercise employed only lasted for around 20–25 minutes, to coincide with the post exercise period and the first part of the WRAT. This point is however speculative and further research would be needed to better understand any temporal effects of exercise on cognitive performance in children. Exercise intensity was determined from the measurement taken from the heart rate monitors. Mean HR was 142 bpm which, when age adjusted, equates to 68% MHR, indicating moderate intensity (categorised as 65–74% of MHR). This intensity has been found to elicit improvements in reading [10], reading comprehension [8] and general improvement in cognitive processing speed [14]. However, in future work more stringent control of exercise intensity may be a factor for consideration. Despite this, the method of exercise employed in the present study is arguably more ecologically valid and practical for class based interventions as compared to either Duncan and Johnson [10] who used a cycle ergometer, or Hillman et al. [8] who employed treadmill based exercise. Physiologically, the acute bout of exercise could have induced increased cerebral blood flow to the brain, with vigorous leg, arm and hand movements evoking marked focal increases in cortical blood flow of the contralateral hemisphere [15], stimulating areas of memory function and brain-derived neurotrophic factor [16]. These changes in cortical blood flow are similar to those induced by memory tasks and visual stimulation [15] and this may be the mechanism whereby cognitive perfor- HUMAN MOVEMENT B.D. Dickinson, M.J. Duncan, E.L.J. Eyre, Exercise and academic achievement in children mance is increased. Endurance exercise, such as circuit style exercise and running, has been proposed to produce a deregulation of the highest level of consciousness associated with the prefrontal cortex and an adverse effect on executive control during exercise [17]. This hypothesis also proposes that all motor cortex activation will cease, and functioning restored, immediately as soon as the altered state, such as that produced by exercise, has ended. Standardised scores achieved could, therefore, possibly be affected not only by timing, and order of the WRAT protocol, but also by efficiency of physical recovery of the individual children. If this is the case, and with reference to the ‘neural interference’ and more cognitive demands for movement reported by Lambourne and Tomporowski [9] it would be advantageous in future research to ascertain the fitness of the children prior to the session. The reporting of positive relations between fitness and standardised achievement test performance [4] and increased performance in core academic classes in children who were able to engage in more vigorous physical activity [5] may imply that fitter children can cope with more neural interference before it affects cognitive function after exercise. In summary, the present study provides no strong evidence that exercise intensity moderates the improvement in pre-adolescent post-exercise academic ability. Exercise was found to improve word reading independent of intensity. Exercise did not improve sentence comprehension, arithmetic, spelling or reading, with the relationship with exercise intensity requiring further investigation. 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Functional neuroanatomy of altered states of consciousness: The transient hypofrontality hypothesis. Consciousness and Cognition, 2003, 12 (2), 231–256, doi: 10.1016/ S1053-8100(02)00046-6 Paper received by the Editor: November 4, 2015 Paper accepted for publication: March 25, 2016 Correspondence address Ben D. Dickinson University of Central Lancashire Preston, United Kingdom e-mail: bdickinson3@uclan.ac.uk 7 HUMAN MOVEMENT 2016, vol. 17 (1), 8 – 14 How the Kenyan runner’s body structure affects sports results doi: 10.1515/humo-2016-0002 Jerzy Eksterowicz *, Marek Napierała, Walery Żukow Faculty of Physical Education, Health and Tourism, Kazimierz Wielki University, Bydgoszcz, Poland Abstract Purpose. The aim of this study was to determine the dependency between somatic parameters of selected Kenyan marathon runners and results achieved in long-distance runs (marathon, half-marathon, 10,000 meters). Methods. The research study was conducted on a sample of 9 top-level long-distance Kenyan runners whose results in Poland correspond to International Masterclass. All runners’ (mean ± SD) age: 23.67 ± 4.41 years, weight: 55.98 ± 4.84 kg, height: 169.18 cm ± 4.15cm. All participants had their anthropometric measurements taken: length, width, size and sum of three skin-folds. Having taken those anthropometric measurements, Body Mass Index (BMI), Arm Muscle Circumference (AMC), Waist to Hip Ratio (WHR), body mass and body fat (FM) (%), fat free mass (FFM) were calculated using the Durnin-Womersley method. Results and conclusions. Significant relations (significant correlation, important dependency) were observed in dependency between 10,000 meters results and the foot breadth (r = 0.765) and torso length (r = 0.755). Similar relationships occurred between marathon results and the arm length (r = 0.73), forearm length (r = 0.75) and hip width (r = 0.77). Key words: somatic characteristics, body composition indices, Kenyan runners Introduction Many sport disciplines show correlation between selection of candidates for a particular sport discipline and somatic features. For instance, the taller the basketball player is, the more rebounds he makes during the game. It comes as no surprise that a basketball player’s height influences the efficiency in basketball. Predisposition for physical competition was a subject of many reports [1–3]. It became clear that not only physical traits (height, width and circumference measurements) play an important role in sport but also body composition: adipose tissue and its location throughout the body, fat free mass or water content in the body etc. [4–5]. Thanks to constant selections of candidates for sport disciplines, it is possible to identify athletes of such a body structure that enables them to score top results and at the same time eliminate athletes with poor results. The athletes’ strong will to beat their personal bests make sport activists and coaches alter their selection criteria and choose the ones that promise masterful results. Particularly interesting with regard to what has been said is the phenomenon of extreme endurance abilities of Kenyan runners who have been ranked among top athletes in middle- and long-distance runs for the last 25 years. Their dominance is reflected in a series of world records set in the majority of endurance events. The laboratory tests revealed that black runners consume more oxygen (at maximum ontogenetic absorption ability) than white * Corresponding author. 8 runners at the same running speed [6–8]. It may lead to an increased utilization of fats while saving glycogen during physical activity as fats need oxygen to be oxidized. The consequence of extremely intensive training and selection of athletes, as not all Kenyans are predestinate for endurance events, is a specific body type that tends to be extremely thin, low in body mass, low in adipose tissue and with not very developed muscle tissue. Is it correct to state that this subpopulation is close to a somatic ideal in selected sport disciplines? Giving an answer to the above question may enrich the knowledge on building an endurance ability with the use of particular body parts. The aim of this study was to determine the dependency between some somatic parameters of selected Kenyan runners and their results in long-distance runs (marathon, half-marathon, 10,000 meters). Material and methods The research sample consisted of nine professional, long-distance Kenyan runners (all black) who for several years took part in a series of running competitions in Poland (street runs, marathons, half-marathons). They ran once a week, every weekend for 5–6 weeks and then they went back to their country. All tested competitors hold leading times for top running events, which in Poland are equivalent to Masterclass. All runners come from the same geographic region, that is the Great Rift Valley in Kenya and train in St Patrick International Sport Club in Iten town. Profile of the runners – (values are given in mean ± SD) age: 23.67 ± years, height: 169.18 ± 4.15 cm, weight: 55.98 ± 4.84 kg. Measure- HUMAN MOVEMENT J. Eksterowicz, M. Napierała, W. Żukow, How the Kenyan runner’s body structure affects sports results ments and calculations were done in July 2013 during the athletes’ presence in Poland, in the civilian-military sports club “Zawisza” in Bydgoszcz. The following anthropometric measurements were taken: length measurements (cm): body height (V–B), arm length (a–r), forearm length (r–sty), upper limb length (a–da III), lower limb length (tro–B), foot length (ap–pte); width measurements: shoulder breadth (a–a), hip width (ic–ic), pelvic width (is–is), hand width (mm–mu), palm width (mr–mu), foot breadth (mtt–mtf); and the circumferences of: fully expanded/deflated chest, waistline, hipline, fully flexed and extended arm muscle, thigh and calf. Measurements of the thickness of three skinfolds were taken in the following body parts: triceps skinfold (TSF), vertical fold, subscapular skinfold (SCSF), horizontal fold, suprailiac skinfold (SISF), diagonal fold. On the basis of those measurements Body Mass Index (BMI) kg/m2 , Arm Muscle Circumference (AMC), Waist to Hip Ratio (WHR), Fat Mass (FM) (kg), Fat Mass (FM)(%), Fat Free Mass (FFM) (kg), Fat Free Mass (FFM) (%) were calculated using the Durnin and Womersley formula [9]. Body Mass was measured on a commercial scale (TANITA BF 662M Japan). The length and width measurements were taken using an anthropometric apparatus. The circumference measurements were taken with the use of an anthropometric tape, the thickness of skinfolds was measured with skinfold calipers. All the measuring instruments were part of an anthropometric apparatus set made by Siber Hegner & Co., Ltd (Switzerland). All measurements were taken by the same investigator, applying standard anthropometric methods according to the procedure of the International Biological Programme [10]. The study was performed according to the Declaration of Helsinki. Written informed consents were obtained from all participants. In order to find some association between the results of long-distance events and results of anthropological measurements Spearman’s correlation coefficient was calculated. Correlation dependency between two characteristics X and Y is distinguished by the fact that merit of one feature is equivalent to median merit of the other feature. The interpretation proposed by the correlation coefficient Guilford is an assessment of the strength (power) of the correlation, to verify the statistical significance of the Student t-test can be used for correlation coefficient. As a result of this test for the sample n = 9 correlation coefficients with a value greater than 0.58 are statistically significant at = 0.05 significance level (below 0.20 – weak correlation, slight dependency; 0.20–0.40 – low correlation, evident dependency but slightly important; 0.40–0.70 – moderate correlation, important dependency; 0.70–0.90 – high correlation, significant dependency; 0.90–1.00 – very high correlation, strong dependency). Subjects of the study were examined taking into consideration two variables: characteristic X (somatic parameters) and characteristic Y (run results). Statistical information crucial for estimating correlation between features X and Y was prepared on the basis of correlation table. Results Table 1 reports the results of anthropological measurements and the results of long-distance events. In Table 2 the results of measurements of tested circumferences and some anthropological features of Kenyan runners are presented. Table 3 shows correlation coefficients between results of the following events: 10,000 meters, half marathon, marathon and selected anthropometric measurements. Important relationships were observed between the following results: important correlation (statistically significant dependency at the level of materiality 0.05) – between results obtained in 10,000 meters run and foot breadth ( = 0.76), and torso length ( = 0.75). Similarly, an important correlation (significant dependency) was observed between marathon results and the following parameters: arm length (r = 0.73), forearm length (r = 0.75), hip width ( = 0.77). A moderate correlation (statistically significant dependency at the level of materiality 0.05) was found between 10,000 meters results and the following parameters: body mass (r = 0.49), BMI (r = 0.43), arm length (r = 0.54), shoulder breadth (r = 0.53), thigh circumference (negative correlation, r = –0.46). The same moderate correlation (important statistically significant dependency at the level of materiality 0.05) was shown in relationship between half marathon results and the following parameters: arm length (r = 0.50), upper limb length (r =0.45), foot length (r = 0.51), hips breadth (r = 0.43), foot breadth (r = 0.54), torso length (r = 0.40), calf circumference (negative correlation, r = –0.43). Moderate correlation (statistically significant dependency at the level of materiality 0.05) was found between marathon results and the following parameters: BMI (r = 0.40), upper limb length (r = 0.58), torso length (r = 0.46), WHR index (r = 0.41). No relationship was observed between results of the examined runs and other somatic parameters. Discussion Black Kenyan and Ethiopian runners have dominated endurance events in recent years. Those athletes mostly come from a high-altitude region of the Great Rift Valley (2300 m above sea level). That region is a homeland of champions who are ranked as the best middle- and longdistance runners in the world. Kenyan runners’ superiority in long-distance runs is often linked to the advantage of living in thinner air (hypoxia), which is the likeliest reason of their increased endurance ability. Presently, Kenyan runners from this region hold most of the world records in the following events: men’s 800 meters, 3,000 meters steeplechase, 5,000 meters, 10,000 meters and marathon; women’s 5,000 meters. 9 HUMAN MOVEMENT J. Eksterowicz, M. Napierała, W. Żukow, How the Kenyan runner’s body structure affects sports results Table 1. Number profile of selected anthropological measurements of Kenyan marathon runners and their results achieved in selected events Tested feature SD Min Max 10,000 meters (s) Half-marathon (s) Marathon (s) Body height (cm) (B–V) Body mass (kg) Fat mass FM (%) Fat free mass FFM (%) 1730.43 3753.61 8080.30 169.18 55.98 5.41 94.59 33.24 67.84 158.59 4.15 4.84 1.75 1.75 1791.0 3840.16 7800.57 161.0 48.0 4.56 90.72 1698.47 3600.15 8280.25 177.0 63.1 9.28 96.83 Sum of skinfolds (mm): – subscap – triceps – suprial 13.97 5.46 4.09 4.42 1.96 1.70 0.81 1.10 11.7 3.5 3.0 3.0 18.5 9.6 5.0 5.0 Length measurements (cm): – arm (a–r) – forearm (r–sty) – upper limb (a–da III) – lower limb (tro–B) – foot (ap–pte) – torso (tro–a) 33.04 26.38 80.51 90.02 25.72 50.96 1.93 2.99 3.80 2.77 0.88 3.20 30.50 23.40 76.40 85.60 24.00 46.00 35.80 27.20 87.10 97.70 26.60 54.30 Width measurements (cm): – shoulder (a–a) – hip (ic–ic) – pelvis (is–is) – hand (mm–mu) – palm (mr–mu) – foot (mtt–mtf) 38.66 28.73 23.02 10.04 8.00 9.77 2.72 1.47 1.21 0.56 0.56 0.68 33.40 26.20 20.80 9.50 7.00 9.00 41.50 31.00 24.60 10.50 9.00 11.20 Numerous scientists, e.g. Temfemo et al. [11], seeking for a reason of such an exceptional endurance ability indicate the difference in quadriceps of white runners and black Kenyan ones. Kenyans have a lot more capillary around microfibers and much more mitochondria. Smaller fibers of African athletes enable mitochondria to approach capillary vessels that encompass fibers, which allow easier oxygen diffusion from capillaries to mitochondria and efficient oxidation. Weston et al. [12] reported that black athletes tend to have increased muscle enzyme levels that burn fat and store glycogen when compared to their white counterparts. This enables them to improve their endurance especially when finishing middle- and long-distance runs. It is worth mentioning that a great density of capillaries and increased number of mitochondria in the muscular system were observed in the inhabitants of other highaltitude regions such as Peru, Mexico and Tibet. Some researchers pay closer attention to Kenyans’ diet [13–14]. The diet is very simple: small portions of fried meat, boiled and raw vegetables, fruit, eggs, milk and their favorite ugali groats. Additionally, they use vegetable sauces, bean, corn, fruit or parts of plant sprouts and sometimes meat. Such a diet contains a lot of carbohydrates, mineral components, vitamins and fibre 10 but lacks fats, especially animal ones. It is worth mentioning that traditionally Kenyans eat 2 meals a day. Most researchers accentuate existence of dependency between consumption of drinks rich in simple sugars and building running endurance and physical capacity in comparison with sportsmen who consume pure water. Burke [15] notices that Kenyans and Ethiopians quite often undertake commonly known eating habits that aim at mobilization of muscle glycogen. It is mostly about periodic reduction of carbohydrates, especially simple ones (glucose, fructose) in the marathon runner’s diet followed by a radical increase in simple sugar supply. It may enhance adaptation to endurance effort and thus improve sports results. According to Beis et al. [16], the improvement in physical capacity and endurance is also related to higher oxidation of simple carbohydrates (aqueous solution of glucose + fructose 60g/h) that leads to better effects than doses of 30g/h or 15g/h. Big portions of simple sugars (> 90g/h) may cause higher production of energy, up to 20–50%. Jeukendrup [17] notices that high physical effort that leads to intensive carbohydrates oxidization, even its high contents, works against harmful consequences of glycemic index (GI). Comparing morphological structures of black and white athletes, we noticed the following somatic charac- HUMAN MOVEMENT J. Eksterowicz, M. Napierała, W. Żukow, How the Kenyan runner’s body structure affects sports results Table 2. Number profile of selected measurements (circumferences) and indicators (anthropologic) of examined Kenyan marathon runners Tested feature SD Min Max Circumference measurements (cm): – chest measurement – aspiration (cm) – chest measurement – expiration (cm) – waist measurement (cm) – hip measurement (cm) – arm measurement – tensed (cm) – arm measurement – relaxed (cm) – thigh measurement (cm) – calf measurement (cm) 87.28 82.53 70.33 85.33 26.06 23.56 47.66 37.84 3.88 4.63 4.52 3.25 2.81 2.16 6.29 6.43 83.00 78.00 64.50 81.00 22.00 21.50 46.00 33.00 94.50 90.00 76.00 91.00 32.50 29.00 47.00 54.10 Indexes BMI AMC Index WHR Index 19.55 22.27 0.82 1.51 2.10 0.05 17.50 20.24 0.78 22.90 27.56 0.92 Examined runners were thin and had low body mass with low anthropological indicators. Table 3. The correlation of selected parameters and results of long-distance runs 10,000 meters Height Body mass BMI Sum of fat-skin folds Adipose tissue % Fat free mass % Arm length Forearm length Upper limb length Lower limb length Foot length Shoulder breadth Hip width Foot breadth Torso length WHR AMC Thigh circumference Calf circumference 0.26 0.49* 0.43* –0.36 –0.36 0.36 0.54* –0.04 0.14 –0.34 0.36 0.53* 0.30 0.76** 0.75** –0.38 0.13 –0.46* –0.19 Half-marathon –0.13 0.17 0.25 –0.06 –0.06 0.06 0.50* 0.08 0.45* –0.37 0.51* –0.15 0.43* 0.54* 0.40* –0.15 –0.05 –0.26 –0.43* Marathon –0.03 0.34 0.40* 0.16 0.16 –0.16 0.73** 0.75** 0.58* –0.13 0.57 0.25 0.77** 0.29 0.46* 0.41* –0.08 0.01 –0.23 * moderate correlation (statistically significant dependency at the level of materiality 0.05) ** significant correlation, important dependency (statistically significant dependency at the level of materiality 0.05) teristics of black runners: lower body mass, significantly lower adipose tissue that results in much lower BMI, longer lower limbs, smaller calf circumference and shorter torso [18]. They certainly increase endurance abilities, especially in endurance events. In our study all the Kenyan runners were distinguished by low BMI (19.55 ± 1.51), low body fat (5.41 ± 1.75%) and slim calves (37.84 ± 6.43 cm). Similar results were published by Knechtle et al. [19] and Kong et al. [20]. In the chosen elite Kenyan runners they noticed low BMI (20.1 ± 1.8), low body fat (5.1 ± 1.6%) and slim legs (34.5 ± 2.3 cm), however in our study a negative correlation between the calf circum- ference and run time was found. The aforementioned authors tested duration of ground contact time during an endurance run and observed the difference between both limbs. They noted that the ground contact time of dominant leg was 170–212 ms, while that of the other leg was longer, about 177–220 ms. The short ground contact time, according to the authors, may be related to the running economy as there is less time needed to stop the front of the body. The differences in ground contact time between both limbs are most likely related to their slightly different functions. According to a biomechanical model for running, 11 HUMAN MOVEMENT J. Eksterowicz, M. Napierała, W. Żukow, How the Kenyan runner’s body structure affects sports results speed depends on a) the step length b) the frequency of gait (v = l × f, where: v – speed, l – length, f – frequency of gait). On the other hand, the step length depends on the length of the lower limbs, flexion angle (to the front side) as well as the extension (to the back side). The step length is also related to the body morphology, however the aforementioned angles depend on movement technique Erdman [21]. If a runner of a certain height of the body has a too long torso, his limbs are relatively shorter. Thus, his step length is going to be shorter as well. Hence, the positive correlation between the run time and the torso length is observed. Whereas, a runner of the same body height but longer lower limbs will make longer steps. This in turn results in negative correlation between the run time and the length of a lower limbs. The step frequency is related to the muscle preparation as well as muscle-nerve stimulation at a certain frequency, especially as far as endurance is concerned. The discussed frequency depends also on overcoming resistances such as: a) limbs inertia and, to less extent, b) the soft tissue extensibility. The limb with a broad expanded foot has a higher moment of inertia. The moment of inertia, among others, is the sum of the foot mass and its squared distance from the rotation axis of the hip-joint. The higher moment of inertia is, the bigger effort must be done by the muscles to move the limbs. Therefore, it is not recommended to have too expanded feet (hence, the positive correlation between the foot size and run time), but it is also not good to have too long lower limbs, because of the too long distance between the foot and the hip-joint, which results in more difficult lower limbs movements. According to the above, too long upper limbs also do not favor a fast and long-term rotary motion around the axis of the shoulder-joint. Hence, the positive correlation between its length and run time. The negative correlation between the thigh circumferences and shinbone is the results of the need for lower limb strength during the run, especially for the 10 km distance. There is no need to have too much basic strength; principally, the muscular endurance is important. Another issue to discuss is the racing tactic, which, among others, consists of speed distribution during the whole distance. Erdmann and Lipińska [22] found that when the best runners were braking the world records for the long-distance runs, their speed distribution was horizontal (the speed was closed to constant) or slightly rising. Whereas, many other runners start the race at excessive speed and then slow down, which results in a worse run time. For runners who have better physiological and morphological predispositions, it is easier to keep the pace steady, close to constant running speed, and have better running times. It is remarkable that three fourth of the best Kenyan runners belong to the Kalenjin tribe [23]. Kalenjin people make up only 12% of Kenya’s population while the Kalenjin tribe makes up around 1/2000 of the world’s 12 population. In recent years Kenyan athletes have dominated the majority of the most important athletic events such as the IAAF World Indoor Championships, World Cross Country Championships, Olympic Games and most famous marathon races. It was estimated that they had won three eighth of all the trophies in middle- and long-distance races. Their achievements were described by specialists as “The highest geographic density of sport achievements ever recorded”. Seeking for reasons of the remarkable endurance abilities of the Kalenjin tribe members, researchers point out that the fundamental factor is living in a high-altitude region (over 2000 m a. s. l.). It seems that people living in thin air for generations have developed acclimatization to hypoxia. Weston et al. [24] points out that living in high-altitude areas always is linked with lowered oxygen concentration. To compensate lack of oxygen, the body has to increase the number of erythrocytes that transport oxygen, which at lower altitudes creates advantageous conditions to increase compound aerobic capacity. Although some reports do not confirm the above findings. The study by Saltin et al. [25] showed no disparity in maximum oxygen consumption (VO2max) of elite Kenyan and Scandinavian runners or unqualified Kenyan runners and a group of young people from Denmark. Further research is needed. According to Larsen [26], members of the Kalenjin tribe are described as people with a higher concentration of those enzymes in skeletal muscles that stimulate better utilization of oxygen and decreased production of lactic acid. As a result of that, the Kalenjins are able to transform oxygen into energy in much more efficient manner. As some authors claim [27], abilities of increased aerobic capacity among the Kalenjins are the results of genetic transfer and odd environmental conditions. If they undergo special training and follow a healthy lifestyle, they become athletes of enormous endurance abilities and absolutely exceptional abilities to regenerate. Thus it is extremely difficult to beat an athlete who, like his ancestors, originates from the highlands of the Great Rift Valley. Generally all researchers agree that the exceptional endurance abilities result from an interaction of genetic heritage, environmental conditions (hypoxia) as well as cultural, social and economic determinants. In view of extremely difficult living conditions, underdeveloped economy and lack of job opportunities, young Kenyans and Ethiopians choose to become athletes. Thanks to their strong will and hard work they become successful in sport all around the world, which improves their and their families’ living standard. Conclusions As a results of conducted study following conclusions were made: 1. The BMI of the examined Kenyan runners was fairly low compared to the health norms, in some cases even below the norm. HUMAN MOVEMENT J. Eksterowicz, M. Napierała, W. Żukow, How the Kenyan runner’s body structure affects sports results 2. The following correlations have been found: – positive (important) – the 10 km run time was correlated with the foot width and torso length, – positive (important) – the marathon run time was correlated with the arm, forearm length, and the hip width, – positive (moderate) – the 10 km run time was correlated with body mass, BMI, arm length, width shoulders, – negative (moderate) – the 10 km run time was correlated with the thigh circumference, – positive (moderate) – between the half-marathon run time was correlated with the arm length, lower limb length, foot length, hip width, foot width, and torso length, – negative (moderate) – the half-marathon run time was correlated with the calf circumference, – positive (moderate) – the marathon run time was correlated with BMI, upper limb length, torso length, and WHR index. References 1. Markovic G., Jaric S., Movement performance and body size: the relationship for different groups of tests. 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Paper received by the Editor: July 23, 2015 Paper accepted for publication: March 30, 2016 Correspondence address Jerzy Eksterowicz Instytut Kultury Fizycznej Uniwersytet Kazimierza Wielkiego ul. Sportowa 2 85-091 Bydgoszcz, Poland e-mail: jekster@interia.pl 14 HUMAN MOVEMENT 2016, vol. 17 (1), 15– 20 The multi-functional foot in athletic movement: extraordinary feats by our extraordinary feet doi: 10.1515/humo-2016-0001 Jennifer Wilson 1 *, John Kiely 2 1 University of Derby, College of Life & Natural Sciences: Sport, Outdoor & Exercise Science, Derby, United Kingdom University of Central Lancashire, Institute of Coaching & Performance, School of Sport, Tourism and the Outdoors, Preston, Lancashire, United Kingdom 2 Abstract The unique architecture of the foot system provides a sensitive, multi-tensional method of communicating with the surrounding environment. Within the premise of the paper, we discuss three themes: complexity, degeneracy and bio-tensegrity. Complex structures within the foot allow the human movement system to negotiate strategies for dynamic movement during athletic endeavours. We discuss such complex structures with particular attention to properties of a bio-tensegrity system. Degeneracy within the foot structure offers a distinctive solution to the problems posed by differing terrains and uneven surfaces allowing lower extremity structures to overcome perturbation as and when it occurs. This extraordinary structure offers a significant contribution to bipedalism through presenting a robust base of support and as such, should be given more consideration when designing athletic development programmes. Key words: foot, degeneracy, bio-tensegrity, robustness The overlooked role of the foot in dynamic sporting activities Conventionally, when devising conditioning strategies to enhance ambulant, bipedal athletic movements – run, jump, pivot, turn, change direction – much training attention is dedicated to strengthening the large powergenerating muscles of the hips and upper legs. Substantial research exists evidencing the positive contributions of various strength and conditioning strategies to athletic performance: to the extent that few would argue against the conventional perspective that, within reason, stronger muscles enhance movement capacity. Within this conventional ‘muscle powers movement’ model there is, we suggest, an apparent omission. Specifically, observable power production, in dynamic locomotive activities, typically exceeds muscular force-generation capabilities. As an example, during the step phase of a triple-jump, impacts of up to 15 times bodyweight and above are commonly absorbed, controlled and the propulsive forces necessary to power the next jump phase are generated, within the abbreviated time-frame afforded by a short ground contact typically lasting less than one-fifth of a second [1]. Similarly, during running, impacts of multiple times bodyweight are comfortably accommodated, by runners of all abilities, for little discernible effort. In elite sprinters very forceful ground contacts must be managed in windows of as little as 80 ms–1 [2]. In non-elite marathon runners, im- * Corresponding author. pacts, while less forceful than those of the sprinter, nevertheless typically number beyond 21 thousand contacts, again of multiple times bodyweight per leg [3]. Furthermore, during the dynamic accelerating, decelerating, twisting and turning athletic movement permutations common across a broad range of sporting activities, the loadings imposed on joints and other structures appear similarly excessive: exposing tissues to high shock loads, in apparently unstable, ever-varying movement conditions. Despite the severe challenges imposed by such dynamically-shifting movement demands, we are capable of robustly and agilely executing a broad diversity of complex bipedal movements, under constantly shifting conditions. A further interesting, if obvious, observation is that although many muscle groups must be skilfully activated to manage, buffer and generate propulsive powers, their net contribution to whole-body momentum can only be expressed through interaction with the ground. A feature of bipedal movement is that the large forces generated through the dynamic re-positioning of the limbs during flight must be transferred between body and ground via the relatively small surface area provided by the foot. The foot serves as our only interface with the ground during walking and running, but also in the endless variety of dynamic movement permutations encountered in athletic sporting activities. Hence the foot is exposed to high shock impacts and decelerations, while simultaneously and/or consecutively functioning as a brake, a spring, a buffer, a means of steering, and a stiff conduit for force transfer between the dynamically moving body, and the immovable environment. Yet despite this primacy, little consideration is typically afforded 15 HUMAN MOVEMENT J. Wilson, J. Kiely, The multi-functional foot Figure 1. A depiction of the three evolutionary innovations that contribute to ‘robustness’ within the foot structure to foot conditioning within our conventional training theory or practices. Over the course of our evolutionary history, the architecture of the foot has been progressively shaped by ever-present evolutionary imperatives, constantly striving to increase movement proficiency, for minimum uptake of energetic and neural resources, while simultaneously reducing exposure to negative sensory feedback indicative of the mounting risk of ‘damage’ [4–8]. The aim of this piece is to highlight three evolutionary innovations which, in combination, underpin the remarkable robustness of the human foot during dynamic impact activities (see Figure 1). Extraordinary feats by our extraordinary feet Neurobiological complexity of the human foot As the only habitually upright bipedal primate, human foot architecture differs substantially from that of our nearest relatives. With three strong arches; over 100 muscles; 26 separate skeletal elements (exempting the sesamoids) linked through 33 joints, fastened by 3 layers of ligaments; dextrously manipulated by numerous intrinsic and extrinsic muscle-tendon units, the human foot constitutes a uniquely complex bio-composite anatomical module [9–11]. This design complexity is not only structural but also sensory. During locomotion the various tissues and structures of the foot are subjected to considerable deformations, in three dimensions. Sensory information, arising from local foot deformations, emanates from multiple somatosensory receptors in the foot arch ligaments, joint capsules, intrinsic foot muscles, and cutaneous mechanoreceptors on the plantar soles: such that deformations instantaneously affect afferent outflow [9, 12–14,]. This neurobiological design complexity is matched by a similarly expansive functional complexity, as the foot adapts to the expansive diver16 sity of tasks imposed by the physics of landing on unpredictable surfaces. In the past, this seemingly needless complex design was frequently considered an unfortunate legacy from our evolutionary past. Yet, despite the intricate nature of its multi-tissue, multiple sensory organ, bio-composite structure, the foot remains highly functional and adaptable. It is remarkably robust, across an unusually diverse range of dynamic movement activities: walking, running, climbing, turning, pivoting, hopping, bounding. Furthermore, not only does the foot adapt to changing movement demands, it also is capable of fulfilling multiple roles, frequently simultaneously, in multiple movement contexts. For example, even under the abbreviated ground contacts afforded during run/jump activities, the foot functions as a flexible structure in early stance, buffering, braking, and stabilizing, yet milliseconds later is a rigid structure, stiffly channelling propulsive forces; directing momentums and contributing to push-off efficiency [14]. Certainly, the foot is not simply a passive, rigid base of support but a flexibly adapting, exquisitely adaptive functional unit: enabling precise control of multiple functions. And, far from being a potentially problematic evolutionary hangover, the complexity of the human foot endows us with a rich repository of robustness and efficiency-enabling movement innovations. Degeneracy: the adaptive agility of the ‘nearly decomposable’ human foot The early complexity theorist Herbert Simon suggested biological organisms could be meaningfully approximated as ‘nearly decomposable’ complex systems. A purely mechanical system is, in contrast, fully decomposable, in that each component fulfils a tightly designated role within a given context [15]. Within a ‘nearly decomposable’ biological system there is obvious crossover, overlap and integrated interplay between the functionality of different tissues and structures in different contexts. Yet, the entire organism is not haphazardly complex and instead exhibiting a modular design: whereby each module is composed of collections of elements more densely networked to each other than to elements within other modules. Modularity is a crucial organizing principle, pervasive throughout biology, greatly simplifying what would otherwise be overwhelmingly disordered complexity. Although all modules are inter-connected, they are simultaneously partially-insulated and functionally semi-autonomous. Hence modularity facilitates robustness as modules can evolve, reshape, rewire and repair in tandem, or independently, without necessarily jeopardizing the survivability of the entire organism [16–18]. This ‘nearly decomposable’ architecture enables complex neurobiological systems to reap the benefits of structural specialization while simultaneously retaining HUMAN MOVEMENT J. Wilson, J. Kiely, The multi-functional foot the adaptive agility essential to coping with demands imposed by a chaotic, ever-changing environment. Such design characteristics underpin an essential prerequisite of biological robustness: degeneracy [19]. Degeneracy is the capacity, of alliances of modules, to collectively modify behaviours and re-combine outputs in differing permutations to collaboratively realize equivalent outcomes through a diversity of pathways [20–24]. In biological terms, degeneracy is similar to, but differs from, the classical concept of redundancy, in that it enables collaborating communities of fundamentally different components to produce consistently reliable outputs under diversely fluctuating conditions [19, 21]. The bio-composite design of the human foot provides a prime example of a highly-degenerate biological architecture. The complex ‘nearly decomposable’ architecture of the foot enables instantaneous structural reconfiguration to dynamically changing contexts. Most obviously in circumstances imposed by environmental variations, such as encountered during running over broken terrains but also during the various permutations of accelerations, decelerations, pivots, turns and changes of direction implicit in dynamic sporting activities. Thus the ‘nearly decomposable’ architecture of the foot facilitates immediate and flexible adaptation to changing context. A further feature of this highly degenerate configuration is that seemingly identical movement cycles, resulting in equivalent movement outcomes, can be achieved through a multiplicity of subtly varying pathways. Thereby enabling the mechanical stresses imposed by repetitive impacts, such as that encountered during a marathon, to be dispersed amongst a broad network of collaborating structural and material components. Hence degeneracy facilitates robustness. Degeneracy within the foot ensures that subtle modifications, in multiple permutations of positioning and/ or pre-tensioning of foot structures, channels mechanical stress through ever-varying routes, thus spreading the work burden imposed by impact and diminishing the probability of repetitive strain, and subsequent tissue damage. The impact of which plays a significant role in ambulant athletic performance. Resisting deformation and channelling momentums: the bio-tensegrity solution The foot is commonly subjected to both frequent, and large, impacts during athletic movements. The degenerate design of the foot substantially contributes to its structural robustness in the face of repetitive shock loadings, yet does not operate in isolation, and is irreparably entwined with another evolutionary design innovation. The architect Buckminster Fuller originally defined tensegrity systems as structures that stabilize shape through continuous tension rather than by continuous compression such as employed, for example, in the construction of a stone arch [25]. In contrast, tensegrity systems innately self-stabilize and resist structural distortion purely by balancing tension-imposing and compression-resisting structural components within a self-stabilizing web of tensioning and stiffening forces [26]. The strikingly energy-efficient, perturbation-repelling simplicity of tensegrity designs has, recently, been recognised as a pervasive evolutionary innovation evident across biological scales, from the cellular to the whole-body level [26, 27]. The bio-tensegrity model depicts the skeletal system as a non-random arrangement of compression elements knitted into the tensional fabric of the fascia [28]. Fascia provides a constant inherent tension maintaining a background tautness that allows the system to respond and adapt to external force without losing the structural integrity of the organism whilst simultaneously serving as a mechano-sensitive signalling system, receptive to pressure changes [29]. The running bio-tensegrity system is composed of a hierarchy of nested subsystems. During dynamic activities, the athletes body acts as a tensegrity system; as does each leg, each muscle-tendon unit (MTU), each muscle, each muscular sub-compartment, each motor unit, each muscle fiber, each myofibril and so on [30–31]. In essence, serving as a sequence of nested tensegrity structures extending down to the level of the individual cell, and beyond. Each nested structure lies within greater, and is comprised of lesser, bio-tensegrity architectures; each evolutionarily designed, structurally and materially, to advantageously respond to the loadings and deformations most relevant to our species survival. Each sub-system innately responds to deformation by striving to rebound to a state of homeostatic mechanical equilibrium: linking from the micro-level of the cell, through the various tissue collectives, to the macro-level of the entire organism [26, 28, 32–35]. The foot, as the structure exposed to the highest impact deceleration, is an exquisitely evolved bio-tensegrity structure. The foot is itself formed by a number of bio-tensegrity systems encased within the foot architecture, and in turn serves as a sub-system of the integrated systemic whole. The foot is often described as being made up of floating compression elements (such as the skeletal structures of the midfoot [36]) supported by a tensional fabric (the plantar aponeurosis being the most cited [37]). Although it is typically considered as having two functional aims – to support body weight and to act as a lever during propulsive phases of locomotion [9] –, thanks to its complex multi-tissue design the foot system is capable of fulfilling a wide diversity of functions: variously absorbing, decelerating, transferring, steering and recycling movement powers. As with any bio-tensegrity system, effective dispersal of forces alleviates risks of exceeding critical tissue loading 17 HUMAN MOVEMENT J. Wilson, J. Kiely, The multi-functional foot limits. To move efficiently these forces must be channelled and re-deployed to optimally contribute to stabilisation and propulsive power demands. Within the hierarchy of tensional systems, compression of local structures creates a ‘non-linear wave’ through the tensional fabric of the global construct resulting in a modification to internal forces through a ‘preflexive’ response [27]. Driven by evolutionary imperatives and repeat practice, we progressively become more skilled at exploiting these built-in mechanical efficiencies. We gradually become more proficient at poising ‘tensioned’ or prestressed tensegrity structures to more productively capitalise on ‘cheap’ sources of control and propulsion merely by matching the physics of the situation to innate deformation-repelling features of our integrated bio-tensegrity design [38]. Furthermore, simply by leveraging properties of the mechanical system, the coordinated harnessing of our nested bio-tensegrity design remedies the inherent information-processing and perturbation-prediction deficits implicit in top-down control [39]. This provides an instantaneous non-neurological, yet skilled, response to sudden perturbation: automatically buffering, re-directing and re-cycling momentums and stabilizing movement, for little energetic or neurological investment. Locally, the foot must respond instantaneously, with zero delay, to variations in contact conditions [38]. When moving at speed, where conditions underfoot are predictable, the variable component may assume a stiffly set posture (i.e. high efficiency but high impact). Under more uncertain conditions, the foot will be less stiffly pre-set, allowing for more flexible absorption of contact to overcome external perturbations. The robust human foot: a collaboration of evolutionary innovations During dynamic loading activities the complex, ‘nearly decomposable’ structure of the human foot provides a robust means of absorbing, distributing, channelling and re-directing the shock loads imposed by violent collision with the external environment. Upon impact the foot deforms as tissue structures variously collapse, compress and stretch under the integrated influence of gravity and ground reaction forces. These deforming forces provide both a challenge and an opportunity. Degeneracy exploits the multi-functionality bestowed by our nested bio-tensegrity architecture, enabling us to solve inevitably unique movement problems through ever-varying movement solutions. Hence, movement variability is an outcome of degeneracy, accounting for the flexible and adaptive behaviours seen in a biotensegrity structure. As with any system demonstrating degeneracy, exploitation of variable configurations and behaviours promotes mechanical efficiency as the system strives for the most economical outcome. By offering more movement options, a degenerate system is able to facilitate stress management through variable permutations. At the level of the foot, the seamless integration of tensional properties regulates the poising and pre-activation of hierarchical structures so as to optimally contribute to the stabilization and energetic requirements of movement. In locomotive activities, particularly those that incur repetitive impacts, the foot serves multiple functional roles. A multi-functionality built among a platform of structural complexity. The generous movement degeneracy, afforded by the human foot, is underpinned by this structural complexity. Together this blend of biotensegrity and degeneracy enable the human foot to adjust, deform, dampen, absorb and productively harness the deformations imposed by ground contact (see Figure 2). Theoretical implications Conventional performance training models are built upon a theoretical assumption that improving strength – specifically of the large lower limb muscles – inevitably enhances bipedal movement proficiency. Our purpose is not to dispute this presumption but to highlight its fundamental limitations as an overarching conceptual framework: specifically in relation to the role of the foot in dynamic bipedal movements. In activities that require the athlete to run, jump, land, accelerate, brake and pivot, the foot must instantaneously respond, to inevitably idiosyncratic permutations of internal and external constraints, in a manner resolving the twin demands of robustness and efficiency. The capacity of the foot to simultaneously fulfil multiple demands is enabled by its design complexity. A complexity underpinning the foot’s highly degenerate capacity to Figure 2. Collaboration between three evolutionary innovations 18 HUMAN MOVEMENT J. Wilson, J. Kiely, The multi-functional foot accomplish similar outcomes through a multiplicity of ever-varying movement permutations. A complexity which, thanks to its nested bio-tensegrity design, innately responds to imposed perturbation by first absorbing, and subsequently repelling, structural and material deformations: thus contributing to self-stabilization and momentum re-cycling. This extraordinary structure plays a fundamental role in damping, dissipating and dispersing shock impacts; in channelling and directing momentums; in seamlessly adapting to movement errors or changing surface conditions; in contributing to energy re-cycling through deformation and restitution. Yet despite the criticality of foot function in bipedal athletic activities, our foot conditioning philosophies remain poorly evolved and the potential importance of developing strategies to optimise foot functionality remain commonly overlooked. As our appreciation of the architectural and functional complexity of the foot continues to grow, so too does an awareness that perhaps conventional foot conditioning and therapy strategies need to evolve in tandem? 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Paper received by the Editor: January 18, 2016 Paper accepted for publication: March 30, 2016 Correspondence address Jennifer Wilson University of Derby College of Life & Natural Sciences: Sport, Outdoor & Exercise Science Kedleston Road Derby, DE22 1GB e-mail: j.wilson1@derby.ac.uk HUMAN MOVEMENT 2016, vol. 17 (1), 21 – 28 Identification of determinants of sports skill level in badminton players using the multiple regression model doi: 10.1515/humo-2016-0004 Janusz Jaworski 1 *, Michał Żak 2 1 Department of Theory of Sport and Kinesiology, Institute of Sport Sciences, Faculty of Physical Education and Sport, University of Physical Education, Krakow, Poland 2 Department of Sports and Recreational Training, Institute of Sport Sciences, Faculty of Physical Education and Sport, University of Physical Education, Krakow, Poland Abstract Purpose. The aim of the study was to evaluate somatic and functional determinants of sports skill level in badminton players at three consecutive stages of training. Methods. The study examined 96 badminton players aged 11 to 19 years. The scope of the study included somatic characteristics, physical abilities and neurosensory abilities. Thirty nine variables were analysed in each athlete. Coefficients of multiple determination were used to evaluate the effect of structural and functional parameters on sports skill level in badminton players. Results. In the group of younger cadets, quality and effectiveness of playing were mostly determined by the level of physical abilities. In the group of cadets, the most important determinants were physical abilities, followed by somatic characteristics. In this group, coordination abilities were also important. In juniors, the most pronounced was a set of the variables that reflect physical abilities. Conclusions. Models of determination of sports skill level are most noticeable in the group of cadets. In all three groups of badminton players, the dominant effect on the quality of playing is due to a set of the variables that determine physical abilities. Key words: badminton, sport training, recruitment and selection Introduction Badminton is one of the most popular racket sports. The origins of badminton date back to the second half of the 19th century. Organizations and associations for badminton players are registered in over 90 countries [1]. This sport has attracted the interest of researchers in many academic fields. Numerous scientific studies have dealt with physiological, biomechanical, somatic and psychological conditions, and badminton movement technique [2, 3]. Other reports have demonstrated health benefits of playing badminton [4]. A comprehensive development of motor abilities is needed to become a successful badminton player. Players often perform jumps, sudden directional changes on the court, a broad range of movements of the upper limbs and changes in body posture [5, 6]. From the standpoint of energy demands, badminton is characterized by movements with very high intensity, alternate with short periods of low-intensity exercise or rest [2, 7]. During the game, energy is largely fuelled by aerobic pathways (around 60–70%), while around 30% of the energy is generated from anaerobic processes [3]. With its total time of the game and the character of exercise during individual actions, badminton can be considered as a speed and endurance sport. Anaerobic exercise during the game of badminton is observed during individual * Corresponding author. actions, whereas aerobic exercise results from the duration of the game and the number of various movement sequences repeated during the game [3, 8]. Another important factor that affects the effectiveness of the game is optimal level of somatic parameters. These problems have been documented for example in [3, 9–10]. These studies have shown that optimal body build of a badminton player is characterized by substantial body height and slim body. The findings obtained in many countries [3, 9] have demonstrated that mesomorphy and ectomorphy should be preferred among badminton players. A specific level of coordination motor abilities is also important in badminton. The complex character of the game requires a perfect performance of movement tasks with high complexity and adaptation to frequent changes in the situation on the court [10, 11–13]. Therefore, similar to combat sports and other games (mainly team sports), badminton is classified in the third (the hardest) category of sports, characterized by the highest level of variability of movement structure, which is attributable to the dominance of external stimuli and open movement structure. The effectiveness of the game of badminton depends on many combinations of the factors which determine the effectiveness of coaching in badminton. In the practice of training, one should take into consideration interactions between genetic and training factors. Therefore, both talent identification and training optimization are of key importance for final success in the sport 21 HUMAN MOVEMENT J. Jaworski, M. Żak, Determinants of sports skill level in badminton players [14]. The basic criterion during development of this type of champion model is always the analysis of key variables in the specific sport, with strong genetic determination [15]. Each “champion model” implies the necessity of using only the variables which can be realistically anticipated over the training. Anticipation of adaptations in this field should be based not only on the knowledge of problems connected with human ontogeny but also on the awareness of individual differences in speed of development of children and young people. Identification of the determinants of the effectiveness of actions is essential for athletic training. Unfortunately, few reports have attempted to find variables which should be preferred in badminton (at each stage of sports training). Furthermore, few studies have examined optimization of sports training [16]. Therefore, the main aim of this study was to examine somatic and functional determinants of sports skill level at three consecutive stages in badminton training. The following questions were addressed in the study: – Which somatic characteristics, physical abilities and neurofunctional abilities are of key importance to the sports skill level in badminton players? – How does the configuration of determinants of badminton performance change at each consecutive stage of the training process? Material and methods The results recorded for 96 badminton players in three training categories: 40 younger cadets (aged 11 to 13 years), 32 cadets (aged 14 to 16 years) and 24 juniors (aged 17 to 19 years) were analysed. Mean experience in competition was 3.8 years in the group of younger cadets, 5.9 years in the group of cadets, and 8.2 years in the junior group. The athletes were from the following sports clubs: MKS „Spartakus” from Niepołomice, UKS „Orbitek” from Straszęcin, LKS „Technik” from Głub czyce, UKS „Sokół” from Ropczyce, UKS „Trójka” from Tarnobrzeg, UKS „Badmin” from Gorlice, UKS „Hubal” from Białystok, MKS „Orlicz” from Suchedniów. Their sports skill level was evaluated indirectly using the ranking lists prepared by the Polish Badminton Association. The lists are updated annually after completion of cycles of tournaments. Players are awarded ranking points based upon their achievements in each tournament, and the ultimate position on the annual ranking list depends on the player’s total score. In the case of the equal number of points or other doubts, the evaluation was supplemented with the expert method. The study was conducted according to the Declaration of Helsinki. Informed consent prior to participation was obtained from children’s parents or guardians and coaches. Each player was informed that they can stop the examination at any moment without giving the reasons for such a decision. 22 Scope of the study Martin’s technique was used to measure somatic parameters: body height, length of upper limb, height in the sitting position from the sitting level to the vertex point, range of the arm with racket during the forehand stroke, shoulder width and hip width. Body mass, lean body mass (LBM) and fat mass were evaluated using TANITA TBF-551 body composition analyser. Flexibility – the depth of the seated forward bend [17]. Amplitude of movements in the radiocarpal joint was measured in the four basic directions in the frontal plane and sagittal plane using a goniometer. The analysis focused on the following tests of motor fitness: a) long jump from standing position – explosive leg strength, b) overhead medicine ball throw (2 kg) with both hands, with legs spread apart – explosive arm strength, c) measurement of hand grip strength – force generated under static conditions, d) measurement of maximal force and perception of half of its value – kinaesthetic differentiation of the force, e) run with changes of directions (envelope run) – running speed, f) 10 × 5-metre shuttle run [17] – ability of quick muscle recruitment, g) endurance shuttle run [17] – cardiovascular endurance, h) sit-ups – abdominal muscle power, i) power tests according to the procedure proposed by Spieszny et al. [18] – 10 × 3-metre shuttle run; overhead medicine ball throw (1 kg) from the kneeling position; “tapping” with the medicine ball (2 kg) – 10 cycles of overhead hitting with the ball held with two hands against the wall and against the ground between the legs spread apart, j) maximal anaerobic power (MAP) was calculated as the product of body mass and standing long jump or overhead medicine forward throw [19]. Coordination motor abilities were also analysed: kinaesthetic differentiation of temporal motion parameters, frequency of hand movements, visual-motor coordination, spatial orientation (free and forced modes), mean reaction time to auditory stimulus (minimal, mean, maximal), mean reaction time to visual stimulus, mean selective reaction time to visual and auditory stimuli (minimal, mean, maximal), movement rhythmization, movement integration, kinaesthetic differentiation (spatial-dynamic parameters). The testing procedure, program settings and characterization of the equipment used for the examinations were described in the monograph by Jaworski [15]. HUMAN MOVEMENT J. Jaworski, M. Żak, Determinants of sports skill level in badminton players Results Statistical analysis 1. Prior to the main statistical analysis, the consistency of the distribution of the variables with normal distribution was verified by means of the Shapiro-Wilk test. 2. In order to reduce the number of variables used in the regression model, we used factor analysis performed previously in the study [20]. The variant of the analysis based on the principal component procedure developed by Hotelling with Tucker’s modification was used, supplemented with Varimax rotation proposed by Kaiser. The variables with factor loading of over 0.5000 were selected for further analyses. 2. Coefficients of multiple determination were used to evaluate the effect of structural and functional parameters on the sports skill level in badminton players. This study used the stepwise regression. Forward selection was adopted as a method for selection of variables introduced to the system. Other variables were qualified only in the situation where it was possible to reject the hypothesis of zero contribution to the model (Snedecor’s F-distribution meets the condition of confidence at the level of 95%, p < 0.05). The variables previously separated using factor analysis were considered as independent, and introduced to the regression model. Analysis of the results was performed by dividing all the variables into the three sets: somatic characteristics and structural-functional ones, coordination abilities, and physical abilities. Each set represented the basis for development of a separate model of multiple correlations with sports skill level. The procedure was repeated for each age group (younger cadets, cadets, and juniors). Calculations were made using Statistica 10.0 PL for Windows software package. The significance level was set at = 0.05. The problem of correlations between the sports skill level of athletes and their morphological aptitudes and motor fitness was attempted to be solved through indepth analysis of the phenomenon based on the interpretation of coefficients of multiple determination. The factor analysis [20] and its pragmatic interpretation allowed for selection of up to 26 variables for these statistical procedures (see Table 1). In the context of the research questions, the most interesting information was provided by the analysis of multiple determination that allows for evaluation of the combined effect of the structural-functional characteristics on the sports skill level in badminton players in different age categories. Determination of the combined effect of variables found through factor analysis seems to be more justified than seeking individual causeand-effect correlations between isolated variables. The results were analysed using the typology that allows for division of all the parameters into the three sets: somatic aptitudes, structural and functional characteristics; coordination abilities; and physical abilities. Each of them represented the basis for development of a separate model of multiple correlations with sports skill level. The procedure was repeated for each age groups (younger cadets, cadets and juniors). In the group of younger cadets (see Table 2), quality and effectiveness of playing are mostly determined by the level of physical abilities. This model is based on the results of two speed and strength tests that evaluate lower limb fitness. They explain 33% of the sports skill level. This system of variables is also reinforced (to a slightly lower extent) by the endurance variable and, to an insignificant extent, by the parameters that determine MAP of the upper limbs and static strength. It is noticeable that most of the tests formed a factor which was conventionally (in previous analyses) termed as comprehensive anaerobic power. The whole system of physical Table 1. Set of variables introduced to the multiple regression model No. Variable No. Variable 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. 16. 17. 18. 19. 20. 21. 22. 23. 24. 25. 26. Body height LBM Shoulder width Arm range (with racket) Flexibility Wrist mobility Kinaesthetic differentiation of temporal parameters Frequency of movements Visual reaction time Auditory reaction time Selective reaction time Rhythmization Movement integration Visual-motor coordination (free mode) Spatial orientation (free mode) Spatial orientation (forced mode) Differentiation of force parameters of motion Standing long jump 10 × 5-meter shuttle run Cardiorespiratory endurance Envelope run MAP, lower limbs MAP, upper limbs Abdominal muscle power Forward medicine ball throw Static strength 23 HUMAN MOVEMENT J. Jaworski, M. Żak, Determinants of sports skill level in badminton players Table 2. Coefficients of multiple determination between sports skill level and morphofunctional variables in the group of younger cadets R R2 Wrist mobility Arm range (with racket) Shoulder width 0.28 0.37 0.47 0.08 0.13 0.22 0.05 0.09 0.15 3.04 2.83 3.27* Coordination abilities Spatial orientation (forced mode) Visual reaction time Movement integration 0.27 0.32 0.36 0.07 0.10 0.13 0.04 0.05 0.06 2.80 2.07 1.79 Motor physical abilities 10 × 5-meter shuttle run MAP, lower limbs Cardiorespiratory endurance MAP, upper limbs Static strength 0.53 0.61 0.66 0.67 0.69 0.28 0.37 0.44 0.45 0.47 0.26 0.33 0.388 0.389 0.393 Group of variables Variable introduced to the model Somatic and structuralfunctional characteristics R 2pop. F 14.26*** 10.53*** 9.02*** 7.06*** 5.92*** The results statistically significant * p < 0.05; ** p < 0.01; *** p < 0.001 Table 3. Coefficients of multiple determination between the sports skill level and morphofunctional variables in the group of cadets R R2 R 2pop. F Flexibility Body height Arm range (with racket) 0.67 0.69 0.71 0.45 0.48 0.51 0.43 0.43 0.44 18.18*** 9.74*** 7.06*** Coordination abilities Spatial orientation (forced mode) Rhythmization Differentiation of force parameters of motion Visual-motor coordination (free mode) Frequency of movements 0.46 0.55 0.64 0.68 0.71 0.21 0.31 0.41 0.46 0.50 0.18 0.24 0.33 0.34 0.36 5.91* 4.62* 4.70* 4.07* 3.46* Motor abilities of physical nature Envelope run Abdominal muscle power Cardiorespiratory endurance 0.66 0.75 0.79 0.42 0.57 0.63 0.39 0.53 0.57 15.71*** 13.87*** 11.16*** Group of variables Variable introduced to the model Somatic and structuralfunctional characteristics The results statistically significant * p < 0.05; ** p < 0.01; *** p < 0.001 Table 4. Coefficients of multiple determination between the sports skill level and morphofunctional variables in the group of juniors R R2 R 2pop. F Somatic and structuralfunctional characteristics Wrist mobility Body height Shoulder width Arm range (with racket) LBM 0.40 0.57 0.68 0.72 0.75 0.16 0.32 0.47 0.51 0.56 0.10 0.22 0.331 0.337 0.340 2.68 3.12 3.47 2.91 2.54 Coordination abilities Selective reaction time Spatial orientation (forced mode) Movement integration Kinaesthetic differentiation of temporal parameters 0.42 0.54 0.62 0.17 0.29 0.39 0.12 0.18 0.23 2.96 2.66 2.53 0.68 0.47 0.27 2.40 MAP, upper limbs Envelope run MAP, lower limbs Abdominal muscle power 0.68 0.77 0.80 0.82 0.46 0.59 0.64 0.67 0.43 0.52 0.55 0.556 12.11** 9.26** 7.03** 5.59** Group of variables Variable introduced to the model Motor abilities of physical nature The results statistically significant * p < 0.05; ** p < 0.01; *** p < 0.001 24 HUMAN MOVEMENT J. Jaworski, M. Żak, Determinants of sports skill level in badminton players ability variables explains around 40% of the quality of playing in the group of beginners. In the somatic model, three variables emerge as more indicative than others: wrist mobility, arm range (with racket) and shoulder width. However, it should be emphasized that only the combination of these three variables is statistically significant and explains 15% of the sports skill level. The effectiveness of playing is even less determined by the structure of coordination ability variables (ca. 6% in general). In this model, the first place is occupied by the spatial orientation test, i.e. reaction to the moving objects, the second by the test of reaction time to visual stimuli, with the variable of movement integration being the least relevant. A diametrically different construction of all the three models is observed in the group of cadets (see Table 3). It is true that the highest explanation percentage for variability of sports skill level concerned the complex of physical abilities, but it consisted of only three parameters. The first was the factor of MAP for the lower limbs, however, in the other test: envelope run. The motor effect for the results of the test explains 39% of the quality of playing at the level of 39%. Composition with the parameter of abdominal muscle power significantly increases the level of the coefficient of determination (53%), whereas integration of another value that determines the cardiorespiratory endurance leads to an insignificant increase in this index. In this form, it explains around 57% of the variance of the sports skill level. Configuration of the somatic model in the group of cadets in the context of the previous sequence of variables that determine the level of motor preparation seems to be relatively logical. The first place in the model was taken by body flexibility. Correlations between the next two parameters, body height and the range of arm with racket, are logical for the discussed coefficient of determination. However, they do not significantly change the level of explanation for the sports skill level which in the whole composition is at the level of 44%. Presence of the characteristics of body height in the model may be also correlated with high variability of morphological age in this group of study participants. The variables which determine coordination abilities also seem to be interesting. The first variable in the model is spatial orientation (forced mode) but with much greater loading that explains sports skill level compared to the group of younger cadets (18%). The whole model is explained by the quality of playing (36%), reinforced by the following variables: movement rhythmization, differentiation of strength motion parameters, visualmotor coordination (free mode), and movement frequency. The significant effect on the level of playing from such a substantial number of factors of motor coordination is symptomatic for this period of development and represents an interesting material for discussion. In the group of juniors, complexation of variables that form the individual models is also interesting compared to the previously characterized groups (see Table 4). The composition of variables that represent physical abilities is most noticeable and accounts for 55% of the quality of playing. The most important component in the model is anaerobic power of the lower limbs, which seems to be logical since at this stage of training process, the success may be determined by speed and force the shuttlecock is hit with. The parameters that determine the efficient movements on the court (envelope tests and MAP test for the lower limbs) are also important. On the one hand, they can determine successful results in the competition, and on the other hand, their lower level may be compensated by the parameters of body size (mainly the range of the arm with racket) or very efficient movements of the racket that result from high mobility (range of motion) of the wrist. The reality of this phenomenon can be supported by the structure of the somatic model, with the first place (10%) taken by the variable that determines the amplitude of wrist movements and body size parameters (body height, shoulder width and range of motion of the arm with racket). In general, the combination of these variables accounts for 34% of the sports skill level. The effect of coordination abilities is weaker at this stage of training. However, it is worth noting that this composition of variables contains parameters of motor coordination with higher degree of organization. The first place is taken in this sequence by selective reaction time, followed by spatial orientation and movement integration and kinaesthetic differentiation of temporal parameters of movement. The whole model determines the sports skill level in juniors at 27%. Discussion The observations conducted in the study were aimed to bridge the gap in the area of complex explorations in terms of multi-aspect determinants of sports skill level of young badminton players. They concerned in particular the effect of structural aptitudes, physical abilities and coordination abilities on the development of competitive competencies with age. This complex concept was supposed to gradually lead to identification, structurization and hierarchization of the determinants of proper status of sports skill level at each stage of the athletic training process in badminton. The principal interpretation of the results was preceded by multidimensional statistical procedures: factor analysis and the Ward’s method [20]. This was used to reduce the initial number of variables and select the relatively independent factors that guarantee high sports skill level. This was connected with the need for identification of “shared factors” necessary to identify a set of variables which lead to a reduction in the dimension and indication of the higher order factors until they are logically explained. Eventually, due to these statistical 25 HUMAN MOVEMENT J. Jaworski, M. Żak, Determinants of sports skill level in badminton players procedures, 26 variables were selected and analysed within three complexes at each stage of the training process. The selected complexes that determine sports skill level in the group of younger cadets indicate that mainly physical abilities contribute to the positive picture of the game, of which the most important is the player’s ability to move on the court. They are connected with performing both the anaerobic and aerobic exercise [3, 8]. In the case of somatic variables constituting the model, it is the whole composition of this group of characteristics that affects sports skill level at a statistically significant level. The importance of these characteristics to the player’s effectiveness was indicated in the literature review in the Introduction section. It was essential for the sake of the analysed problems to have identified the cause-and-effect relationships between physical abilities and morphological characteristics. Similar relationships were emphasized by Subramanian [21]. In this group, the factor of motor coordination is getting to be more pronounced but mainly in terms of spatial orientation and reaction time to visual stimuli. In general, playing in the group of younger cadets is based on strong physical abilities. A completely different structure of the model was observed in cadets. The number of components of motor coordination in this group rose to five. The importance of coordination abilities for badminton players is also confirmed by the findings published by many authors. Jaworski and Żak [10] analysed morphofunctional models in three groups of experience level. In the model obtained for younger cadets, only the results of movement integration and mean reaction time to visual stimulus were above the mean obtained for the whole module. These results demonstrate that the above coordination abilities are essential for recruitment of athletes, whereas sports skill level is determined mainly by physical abilities and wrist mobility. The dominant abilities in the group of cadets were spatial orientation and visual-motor coordination. In the group of juniors, an average level of contribution to the development of sports skill level was observed for spatial orientation, mean selective reaction time, movement integration and kinaesthetic differentiation. Badminton is numbered among one of the fastest racket sports. Therefore, reaction time is one of the most important neurofunctional abilities that affect playing efficiency. Badminton players (both boys and girls) have better results compared to untrained peers [13]. As presented by the authors of the above study, the findings may have been caused by playing badminton. The importance of visual information processing and time needed to anticipate movement, as well as determination of intercorrelations between these variables in elite badminton players was emphasized by Poliszczuk and Mosakowska [12]. In their study, the researchers used two tests from the Vienna Test Battery: anticipation of movement (ZBA) 26 and visual field (PP). They found a relatively extensive range of vision in badminton players (172.9°, with 89.99° for the left eye and 82.86° for the right eye) and significant correlations between the base indices for both tests. Badminton is a sport where players have to respond to strong and fast shots performed by the opponents using the upper limbs. The results of many studies have shown that shorter reaction time in elite athletes compared to other badminton players may be a key variable to distinguish between players at different sports skill levels. Furthermore, the results of the studies concerning the relationships of simple and complex reaction time with muscular strength show that only complex reaction time was significantly correlated with the strength of the right and left arm and was not correlated with the strength of the lower limbs [22–25]. The review of some selected findings suggests the necessity of paying particular attention to development and improvement of technique in this period of training. Coordination exercises are known to stimulate development of special fitness, which, based on feedback, improves the level of coordination skills. In particular, this might concern spatial orientation, which is essential for evaluation of the trajectory of the shuttlecock in space and observation of the current situation on the court. In the context of the game, it also seems essential to maintain the specific rhythm of actions and the actionrelated frequency of movements. These may include very fast sequences of repeated actions. Good differentiation of force parameters of movement revealed in the factor helps using the racket, whereas visual-motor coordination makes it easy to anticipate the shuttlecock trajectory and hit the shuttlecock with the racket. The most substantial contribution in this group was observed for the complex of physical abilities, but it was dominated by another test, i.e. the envelope test. However, it should be emphasized that the result of this test is associated not only with the speed of recruitment of energy sources but also with motor coordination (fast and rhythmic changes in the direction of movements). This phenomenon can be associated with the structure of the model in the area of coordination abilities. Also the contribution of the abdominal muscle strength test should be regarded as logical as it is associated with improvement in smashes and clears. The dominant orientation of training towards technique development is insufficient to fully utilize the factor of endurance, which in this phase of development starts playing an essential role in the game [3]. The somatic model of a cadet showed substantial differences in the components of body size. The attention should be paid to the component of flexibility, which was located at the first place. This element seems to be useful for solving tasks on the court. The importance of flexibility for playing effectiveness was also emphasized by Subramanian [21]. In the multiple regression model, this variable explained around 10% of the de- HUMAN MOVEMENT J. Jaworski, M. Żak, Determinants of sports skill level in badminton players pendent variable. The second place in the proposed model was taken by speed (around 8%). The analysed model also included arm length and quality of service and attack. All the variables introduced to the model explained around 33% of the playing effectiveness. The importance of somatic aptitudes and flexibility for the quality of playing was also emphasized by Jeyaraman and Kalidasan [26]. In their multiple regression model, the whole model explained around 81% of the playing effectiveness. It should also be emphasized that the age of cadets extends over the puberty period, when a decline in the value of this anatomical and functional parameter is more pronounced. Consequently, this might cause a high dispersion of results. Correlation between body size and sports skill level points to a significant role of the developmental age in earlier achievement of better results in competition. This thesis is reinforced by the strongly accentuated views on the variation of the morphological age and its effect on the results achieved in terms of performance of motor tasks. The greatest variation of physical development was observed in the puberty period, which, in extreme cases, may reach the span of eight years. Since the group of juniors was aged from 14 to 16 years, the relationships found in the study seem to be obvious. Slightly better sports results in this group were obtained by accelerants and individuals who were genetically programmed to be tall. Therefore, the factor of the morphological age must be taken into consideration in the athletic training to understand the causes of developmental delay or accelerations. This problem was also emphasized in studies by Waddell and In Hong [27]. They highlighted the importance of adjusting the exercises to developmental abilities of children and reasonable (rational) development of the technique which is consistent with physical abilities of young badminton players. The system of variables in the models that describe the determinants of the sports skill level in the group of juniors also turned out to be interesting and slightly different than in younger groups of badminton players. At this stage of training process, physical abilities remain to be essential, which is especially noticeable in the dominant variable of MAP of the arms. This phenomenon is logical since juniors do not only have well-developed technique but also the speed and force of hitting the shuttlecock that are necessary at this stage. Furthermore, the efficient shots require fast moving on the court in order to adopt a specific position in time and space. This determines a high level of MAP of the lower limbs, which manifests itself in, for example, the envelope run [19]. The movement actions typical of performance of these tests are immanent in the effective playing. The composition of variables in the somatic model of junior was connected with the range of arm motion, which can often compensate for the deficiencies in effective movements on the court. However, the variable of wrist mobility was dominant. This can be justified by the fact that this helps a player to generate initial speed and force applied to the shuttlecock. There is also the problem of coordination abilities which are slightly weakened at this stage of training. This might be the effect of lower dispersion of the results and consequently, equalization of their level in this group of players, although it should be also emphasized that these abilities are of higher level of organization like selective reaction time, reaction to the moving object, movement integration and kinaesthetic differentiation. These abilities have a leading effect on development of technique of movements of higher order, typical of the effective playing at this level of training process. Conclusions 1. All the models of sports skill level determination are most pronounced in the group of cadets, less pronounced in the group of juniors and the least in younger cadets. 2. In all three groups of young badminton players, the dominant effect on the quality of playing is due to a complex of variables that determines physical abilities. 3. 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Natl J Physiol Pharm Pharmacol, 2015, 5 (1), 18–20, doi: 10.5455/njppp.2015.5.080720141. 26. Jeyaraman R., Kalidasan R., Prediction of playing ability in badminton from selected anthropometrical physical and physiological characteristics among inter collegiate players. Int J Adv Innov Res, 2012, 2 (3), 47–58. 27. Waddell D.B, Badminton for children based on biomecha nical and physiological principles. In: Hong Y., Johns D.P., Sanders R. (eds.) 18th International Symposium on Biomechanics in Sports. Hong Kong June 25–30. Department of Sports Science and Physical Education. The Chinese University of Hong Kong, Hong Kong 2000, 837. Paper received by the Editor: January 27, 2016 Paper accepted for publication: March 31, 2016 Correspondence address Janusz Jaworski Zakład Teorii Sportu i Antropomotoryki Wydział Wychowania Fizycznego, Instytut Sportu Akademia Wychowania Fizycznego al. Jana Pawła II 78 31-571 Kraków, Poland e-mail:wajawors@cyf-kr.edu.pl HUMAN MOVEMENT 2016, vol. 17 (1), 29– 35 Body stability and support scull kinematic in synchronized swimming doi: 10.1515/humo-2016-0008 Alicja Rutkowska-Kucharska*, Karolina Wuchowicz Department of Biomechanics, University School of Physical Education, Wrocław, Poland Abstract Purpose. The aim of this study was to examine the dependencies between support scull kinematics and body stability in the vertical position. Methods. The study involved 16 synchronized swimmers. Twelve markers were placed on the pubic symphysis, head, middle fingers, and transverse axes of upper limb joints. Support scull trials were recorded at 50 fps by cameras placed in watertight housings. Calculated measures included: excursion of the sculling movement; flexion and extension angle of the elbow and wrist joints; adduction and abduction angle of the shoulder joint; adduction and abduction angle of the forearm to/from the trunk; ranges of movement of the wrist, elbow, and shoulder joints; range of movement of forearm adduction towards the trunk; and the range of movement of shoulder adduction towards the trunk. Results. The length of the trajectory taken by the marker on the pubic symphysis was longer if the range of movement of the wrist joint was larger. The movement of the body in the right-left and upwards-downwards direction increased together with a greater range of movement of the wrist joint. It was also found that a greater sculling angle produced greater body displacement in the forwards-backwards direction. The head marker was characterized by a significantly larger range of displacement in the forwards-backwards and right-left directions than the pubic symphysis. Conclusions. The findings indicate that the ability to maintain body stability in the vertical position is associated with the range of movement of the radial wrist joint, angle of forearm adduction, and a newly-introduced measure – sculling angle. Key words: sculling, vertical position, swimmer Introduction The relatively small (compared with other sports) number of scientific publications on synchronized swimming can be explained by the fact that it is still a new, albeit rapidly growing, discipline. A review of the available literature finds reports that have attempted to: determine the total duration and number of times swimmers spend underwater during a solo routine [1], measure the effects of propulsive sculling action in horizontal body displacement [2], compare the efficiency of repetitive arm movements by synchronized swimmers and artistic gymnasts [3], measure the force produced in standard and contra-standard sculling [4], search for a relationship between eggbeater kicking skills with leg and trunk muscle strength and the technical skills needed to maintain the vertical position [5], determine unhealthy behaviors in swimmers and examine the relationships between perfectionism, body esteem dimensions, and restrained eating [6], assess the effects of vibration and stretching on passive and active forward split ranges of motion [7], and evaluate the dynamic asymmetry of support sculling [8]. However, few studies have dealt exclusively with analyzing the synchronized swimming technique. One reason may stem from the necessary albeit complex demands of recording synchronized swimming movements underwater. * Corresponding author. Synchronized swimming is a branch of swimming in which swimmers compete by executing a specific movement routine composed of numerous technical elements. This discipline is dominated primarily by movement sequences performed in an upright (vertical) position, with the head above or under water. A more comprehensive literature review found a limited number of studies analyzing lower limb movements such as the eggbeater and boost kicks, techniques which allow swimmers to move or rise out of the water or maintain the body in the vertical position [9–11]. Some congruency between these swimming techniques and those used in water polo was found [12]. However, few have examined the employment of the upper limbs in synchronized swimming. Although the use of the upper limbs when underwater (termed as sculling) is not subject to scoring during competition, the upper limbs are essential in synchronized swimming performance as they allow a swimmer to execute various movement routines and figures in both static and dynamic conditions. Two commonly executed sculls are the standard scull and support scull. The standard scull (and contra-standard) is used to align the swimmer’s body in the layout position whereas the support scull is employed to maintain the vertical position, with the head above or under the water. Support scull has been described as one of the most difficult techniques in synchronized swimming since it involves steadily and smoothly displacing the body while maintaining a part of it above the water [13]. During vertical position maintenance, with head above 29 HUMAN MOVEMENT A. Rutkowska-Kucharska, K. Wuchowicz, Body stability in synchronized swimming the water, correct sculling technique requires an elbow flexion angle of 90° while maintaining the arm in a relatively stationary position with the forearm performing the sculling motion [14]. Conversely, in order to keep the swimmer’s body in the vertical position with head under the water, swimmers hold their elbows und upper arms stationary whereas the forearms are kept horizontally at 110–145° of elbow flexion [13]. Analysis of support scull kinematics in the vertical position (head under water) was found to differ depending on the length of the lower limbs [15]. During sculling the hands of swimmers typically execute a “figure 8”, eggshaped oval, or ellipse movement [2, 16]. Another alternative is to use hand dorsiflexion. Some sculls, such as the reverse, dolphin, and alligator sculls use a technique involving palmar flexion. Sculls performed with both palmar and dorsal flexion allow swimmers to rotate and twist when in the vertical position [17]. One study to date has attempted to determine the most efficient hand configuration for generating maximal lift by hydrodynamic analysis [16]. Additional interest in sculling technique stems from the fact that synchronized swimming is a subjectively judged sport, where criteria such as the accuracy in executing various figures as well as the ability to maintain the body in a high and stable position above the water are very important. Furthermore, the difficulty in learning the necessary skills to support the body in the inverted vertical position, which takes up to two years according to coaches, warrants additional research on synchronized swimming technique and the ability of the swimmer to maintain body stability in the water. A review of the available literature shows no investigation on the correlations between the kinematic variables associated with support scull technique and balance. One available publication has analyzed the kinematic variables of sculling in elite synchronized swimmers able to maintain nearly perfect body balance, leading them to create an elite movement model but this is based on swimmers that demonstrated proficient and balanced support scull [10]. The difficulty in learning the necessary skillset to support the body in the inverted vertical position can take up to 2 years according to coaches and therefore warrants the need for additional research on support scull technique in order to ascertain technique efficacy. Therefore, the aim of the present study was to search for correlations between support scull kinematics (with the introduction of a new angular variable to quantify the support scull movement cycle) and the ability to maintain balance in the inverted vertical position. Although the biomechanical investigation of synchronized swimming technique – in contrast with competitive swimming [18] – is not directly associated with achieving competitive success, it can aid in the identification of the factors responsible for technique execution and therefore contribute to enhanced performance. 30 Material and methods The sample consisted of 16 female synchronized swimmers with varying levels of performance, from beginners (juniors) to experts (master class). Mean (± SD) age, body mass, and body height was 15.9 ± 3.5 years, 51.9 ± 6.2 kg, and 160.6 ± 6.2 cm, respectively. Written informed consent was obtained from the guardians of the participants as was approval from the local ethics advisory committee. Optimum conditions were ensured in order to provide high-quality data acquisition [19]. Two digital JVS video cameras recording at 50 fps and 100 Hz, placed in watertight housings, were affixed perpendicularly to the walls of a pool. A frame of reference in the shape of a rigid cube (1 m/1 m/1 m) with six selected reference points was used during filming. Both cameras were synchronized with a flash of light. Twelve markers (Figure 1) were drawn on the swimmers’ bodies corresponding to the transverse axes of the shoulder, elbow, wrist, and hip joints and on the pubic symphysis, head, and right and left middle fingers. The markers were 1 cm in diameter and drawn with a waterproof pen directly on the body. Each participant was then filmed performing Figure 1. Location of body markers to define flexion and extension angle of the wrist joint ( ), flexion and extension angle of the elbow joint ( ), adduction and abduction angle of the shoulder joint ( ), adduction and abduction angle of the forearm to/from the trunk ( ), sculling angle( ) HUMAN MOVEMENT A. Rutkowska-Kucharska, K. Wuchowicz, Body stability in synchronized swimming three trials of eight support scull cycles with both lower limbs extending out of the water. The experiment was preceded by a warm-up and all participants wore swimsuits, caps, swimming goggles, and nose clips. Support scull kinematics was quantified using SIMI Motion® software by assessing individual movement cycles. Since sculling is performed in all three anatomical planes, the breakdown of this movement based on only the angle created by the elbow joint was considered insufficient. Therefore, we adopted the angular motion made at both the elbow and wrist joints (measured by the shoulder, elbow, and middle finger markers). This angle was defined herein as the sculling angle ( ). The sculling movement cycle was then delineated by the changes in the sculling angle, where the first phase of the sculling movement cycle was treated as the minimum to maximum sculling angle and the second phase of the sculling movement cycle as the maximum to minimum value. Based on these phases, the following temporal and kinematic characteristics of the sculling movement cycle were considered: – duration of the sculling movement cycle [s] – duration of the first and second sculling cycle phases [s] – trajectory length of the sculling movement (based on the displacement of the middle finger marker) [m] – flexion (palmar flexion) and extension (dorsiflexion) angles of the wrist joint ( ) [°] – flexion and extension angles of the elbow joint ( ) [°] – adduction and abduction angles of the shoulder joint ( ) [°] – adduction and abduction angles of the forearm to/from the trunk ( ) [°] – sculling angle ( ) [°] – ranges of movement of the radial wrist, elbow, and shoulder joints [°] – range of movement during forearm adduction towards the trunk [°] – range of movement during shoulder adduction towards the trunk [°] The angles defined in the study are shown in Figure 1. Body stability during the support scull was assessed by measuring: – trajectory created by the head and pubic symphysis markers (over subsequent scull cycles) – marker displacement in the forward–backward (frontal plane), right–left (sagittal plane), and upward– downward (transverse plane) directions (for each scull cycle) [m]. Statistical analysis was performed using Statistica v 9.1 software. Means and standard deviation were calculated for all variables. The one-sample Kolmogorov– Smirnov test was used to examine the normality of data distribution. Non-parametric measures were then applied (Wilcoxon signed-rank and Spearman’s rank correlation tests). Differences were considered significant when the probability was at p 0.05. Results For this purpose, the mean displacement of the two markers placed on the pubic symphysis and on the head was calculated in three anatomical planes. Additionally, another criterion was the measurement of the length of the trajectory taken by the markers located on the pubic symphysis and head (Table 1). To research the relationship between the kinematic variables of sculling and body stability the criteria for assessing body stability should be determined. The first criterion was the displacement of the swimmer’s body in three directions. Differences in upward– downward displacement and trajectory length of the head and pubic symphysis markers were not statistically significant. However, the head marker was characterized by significantly (p 0.05) greater range of displacement in the forward–backward and right–left directions than the pubic symphysis. This finding suggests the important role of head movement in correcting sway when submerged under the water. For the remainder of the present study we assessed body stability with the pubic symphysis marker. Analysis of the angles as well as ranges of movement found the largest range of movement was exhibited in forearm adduction (Table 2). This movement was also found to feature the smallest variability among the swimmers. The smallest range of movement yet with the Table 1. Mean displacements and trajectory lengths (per scull cycle) by the pubic symphysis and head markers Variable Direction Head marker Displacement (m) Trajectory length (m) Pubic symphysis marker Head marker Pubic symphysis marker * statistically significant difference p Forwards–backwards Right–left Upwards–downwards Forwards–backwards Right–left Upwards–downwards Mean ± SD 0.044 ± 0.010 0.028 ± 0.007 * 0.034 ± 0.015 * 0.028 ± 0.016 0.023 ± 0.010 0.034 ± 0.010 0.13 ± 0.06 0.12 ± 0.09 Coefficient of variation (%) 23.54 25.33 43.66 58.00 45.66 29.67 51.19 65.52 0.05 31 HUMAN MOVEMENT A. Rutkowska-Kucharska, K. Wuchowicz, Body stability in synchronized swimming greatest amount of variability was found in the wrist joint angles. For the sculling angle, the first phase (lateral shoulder movement) was significantly (p 0.05) shorter in duration than the second phase (medial shoulder movement) (Table 3). Correlational analyses were performed between the range of displacement and the trajectory of the pubic symphysis marker (Table 1) and scull kinematics (Table 2). A statistically significant relationship (Spearman’s r = 0.621, p < 0.01) was found between the trajectory of the pubic symphysis marker and radial wrist joint range of movement. The range of displacement of the pubic symphysis marker (and thus the body of the swimmer) in the right–left direction was positively correlated (Spearman’s r = 0.602, p < 0.013) with the range of movement of the wrist joint and negatively correlated (Spearman’s r = –0.720, p < 0.001) with forearm adduction towards the trunk. Movement in the forward–backward direction correlated (Spearman’s r = 0.547, p < 0.028) with sculling angle, whereas upward–downward movement correlated (Spearman’s r = 0.614, p < 0.011) with the range of movement of the radial wrist joint. Comparisons were made between the angular kinematics of those who presented the least (A) and most (B) sway (best and worst stability, respectively) in order to determine a frame of reference for support scull technique. The trajectory length of the pubic symphysis marker in one support scull cycle in the least stable swimmer (B) was 0.10 m, whereas the swimmer with the greatest stability (A) showed only 0.05 m sway. The displacement of the pubic symphysis marker in swimmer B in all three anatomical planes was twice as large as that in swimmer A. The differences in sculling technique by swimmers A and B are illustrated in Figure 2, which presents the trajectories of the right and left middle fingers in all three anatomical planes. Differences between both swimmers were also found in the shape of the trajectories as well as in the amount of upper limb asymmetry. Discussion The purpose of this study was to describe the movement technique used in sculling and determine the kinematic variables associated with maintaining stability in the inverted vertical position. For this purpose, we proposed the division of the sculling movement into cycles and phases by the use of a newly introduced measure, the sculling angle, calculated by the movement of the elbow and wrist joints. The minimum and maximum angular values were used to quantify the entire sculling movement into an initial phase (abduction and second phase (adduction). However, the linear and angular values we obtained are difficult to compare with the results of other authors as different criteria were used to quantify the sculling movement. Nonetheless, a comparison of the duration of the sculling movements found that the present support scull cycle times were similar to the ones reported in other papers [20, 21, 15]. The Table 2. Range of movement (º) for the right and left limb during a sculling movement Right upper limb Range of movement Sculling ( ) Elbow joint ( ) Wrist joint ( ) Forearm abduction/adduction ( ) Arm abduction/adduction ( ) Left upper limb Mean ± SD (º) Coefficient of variation (%) Mean ± SD (º) Coefficient of variation (%) 57.05 ± 10.96 50.61 ± 10.77 26.80 ± 5.65 91.67 ± 7.65 30.84 ± 4.25 19.20 21.27 21.07 7.66 13.76 56.38 ± 13.30 49.99 ± 19.15 31.15 ± 9.6 91.77 ± 7.8 30.83 ± 4.82 23.6 38.3 30.72 8.5 15.65 Table 3. Linear variables of upper limb movements during a sculling movement Variable Upper limb Duration of sculling (s) Duration of the first phase of sculling (s) Duration of the second phase of sculling (s) Trajectory length of the hand (m) Duration of sculling (s) Duration of the first phase of sculling (s) Duration of the second phase of sculling (s) Trajectory length of the hand (m) * statistically significant difference p 32 0.05 Right Left Coefficient of variation (%) Relative time (%) 0.72 ± 0.05 0.31 ± 0.06 * 0.40 ± 0.06 1.74 ± 0.21 7.32 17.96 14.43 15.15 100 43 55.5 – 0.73 ± 0.05 0.28 ± 0.05 * 0.44 ± 0.05 1.64 ± 0.25 6.98 18.18 11.91 15.21 100 38 60 – Mean ± SD HUMAN MOVEMENT A. Rutkowska-Kucharska, K. Wuchowicz, Body stability in synchronized swimming Figure 2. Hand movement trajectory lengths (m) (based on the right and left middle finger marker) for each anatomical plane in the swimmers with the best and worst support scull body stability 33 HUMAN MOVEMENT A. Rutkowska-Kucharska, K. Wuchowicz, Body stability in synchronized swimming present sample of synchronized swimmers showed little variability in sculling movement cycle duration. However, the time of the first and second sculling cycle phases were found to substantially differentiate the swimmers. A comparison of the swimmers with the greatest and least amount of stability indicated that the swimmer with the most sway presented prolonged movement cycle and phase duration. For comparison purposes, the Olympic silver medalists examined by Homma and Homma [13] featured a shorter sculling movement cycle (0.69 s) than the best swimmer in this study, indicating a relationship between scull cycle duration and competitive level. In addition, Rostkowska et al. [21] also demonstrated an association between the duration of the entire movement cycle and performance level, suggesting that swimmers who have trained for a longer period of time and achieved greater success exhibit reduced support scull movement time. Analysis of the angular kinematics in sculling was delineated to the examined ranges of movement. The greatest range of movement was observed in the adduction and abduction of the forearm. This range of movement was also characterized by the smallest variability among the swimmers. Homma and Homma [15] investigated the minimum and maximum angular values and ranges of movement in synchronized swimming. While their results on wrist joint flexion are congruent with that observed in the present study, a number of differences were found between both studies regarding the movement ranges of the elbow joint. This may be explained by differences in the skill level of the samples, where the elite athletes exhibited greater palmar and dorsal flexion whereas the lower-level swimmers in the present study showed no dorsal flexion [15]. This finding highlights the importance of training hand dorsiflexion, as it likely to influence sculling efficacy. To our knowledge, no studies have yet analyzed the kinematic factors that affect body stability in synchronized swimming. This is surprising, as judges assess the ability to maintain the non-submerged parts of the body in a stable upright position over the water [17]. We assumed that one valid measure of body stability in support scull may be the displacement and ranges of movement of the pubic symphysis in all three anatomical planes, as this anatomical location is the closest to the body’s overall center of gravity. We found that this point on the body was characterized by greater movement variability than the head, although the head marker was characterized by significantly greater displacement in the forward–backward and right–left directions than the pubic symphysis. This may indicate the important role of head movement in correcting the body’s stability when upside down underwater. The present findings confirm the importance of fine hand movements in maintaining stability in the vertical position. In particular, we found that an increase in the excursion of the pubic symphysis marker was paralleled with an increased 34 range of movement of the wrist joint, as was the movement of the body in the right-left and upward-downward directions. Furthermore, a larger sculling angle was associated with greater body displacement in the forward– backward direction. This finding implies that excessive flexion of the upper limbs at the elbow and wrist joints during support scull results in a loss of forward–backward stability. In turn, reduced range of movement of the forearm in relation to the trunk correlated with greater displacement in the right–left direction. These findings were confirmed regardless of whether they were performed by the swimmers featuring the greatest or least stability in the vertical position (albeit the latter was characterized by greater sculling asymmetry). Conclusions The use of a sculling angle, as proposed herein, can serve as a valid measure for dividing the upper limb movements of support scull into phases. Additionally, the trajectory and range of displacement of the pubic symphysis can also quantify body stability in the vertical position. Body stability in the vertical position was associated with the range of movement of the radial wrist joint, angle of forearm adduction, and sculling angle. Acknowledgements This study was made possible by the financial support of the Polish Ministry of Science and Higher Education (Grant Nr. 0338 /B/P01/2010/39). References 1. Alentejano T., Marshall D., Bell G., A time-motion analysis of elite solo synchronized swimming. Int J Sports Physiol Perform, 2008, 3 (1), 31–40. 2. Arellano R., De la Fuente B., Domninguez R., A study of sculling swimming propulsive phases and their relationship with hip velocity. In: Anderson R., Harrison D., Kenny I. (eds.), Proceedings of the 27th International Conference on Biomechanics in Sports. University of Limeric (Ireland), Limeric 2009. Available from: http://www3. ul.ie/isbs2009/ISBS2009Proceedings.pdf. 3. Chairopoulou L., The effect of movement rhythm on performance in synchronized swimming and gymnastics. Serb J Sports Sci, 2009, 3 (4), 157–164. 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Rostkowska E., Habiera M., Antosiak-Cyrak K., Angular changes in the elbow joint during underwater movement in synchronized swimming. J Hum Kinet, 2005, 14, 51–66. Available from: http://www.johk.pl/files/05rostkowskain. pdf. Paper received by the Editor: November 4, 2015 Paper accepted for publication: February 8, 2016 Correspondence address Alicja Rutkowska-Kucharska Department of Biomechanics University School of Physical Education al. I.J. Paderewskiego 35 51-612 Wrocław, Poland e-mail: alicja.rutkowska-kucharska@awf.wroc.pl 35 HUMAN MOVEMENT 2016, vol. 17 (1), 36– 42 A comparison of static and dynamic measures of lower limb joint angles in cycling: Application to bicycle fitting doi: 10.1515/humo-2016-0005 Rodrigo Rico Bini 1, 2 *, Patria Hume 2 1 School of Physical Education of the Army, Center for Physical Training of the Army, Rio de Janeiro, Brazil Sport Performance Research Institute New Zealand, Auckland University of Technology, Auckland, New Zealand 2 Abstract Purpose. Configuration of bicycle components to the cyclist (bicycle fitting) commonly uses static poses of the cyclist on the bicycle at the 6 o’clock crank position to represent dynamic cycling positions. However, the validity of this approach and the potential use of the different crank position (e.g. 3 o’clock) have not been fully explored. Therefore, this study compared lower limb joint angles of cyclists in static poses (3 and 6 o’clock) compared to dynamic cycling. Methods. Using a digital camera, right sagittal plane images were taken of thirty cyclists seated on their own bicycles mounted on a stationary trainer with the crank at 3 o’clock and 6 o’clock positions. Video was then recorded during pedalling at a self-selected gear ratio and pedalling cadence. Sagittal plane hip, knee and ankle angles were digitised. Results. Differences between static and dynamic angles were large at the 6 o’clock crank position with greater mean hip angle (4.9 ± 3°), smaller knee angle (8.2 ± 5°) and smaller ankle angle (8.2 ± 5.3°) for static angles. Differences between static and dynamic angles (< 1.4°) were trivial to small for the 3 o’clock crank position. Conclusions. To perform bicycle fitting, joint angles should be measured dynamically or with the cyclist in a static pose at the 3 o’clock crank position. Key words: bike fitting, joint kinematics, photogrammetry, videogrammetry Introduction Optimal body position on the bicycle has been suggested to reduce injury risk and improve cycling performance [1, 2]. The configuration of bicycle components to the cyclist (bicycle fitting) has been usually conducted using tape measures and plumb bobs [3] with the dimensions of bicycle components related to anthropometric dimensions of the cyclist [4, 5]. For the configuration of bicycle components (e.g. vertical and horizontal positions of the saddle), joint angles have been preferably recommended in comparison to anthropometric references [6]. The reason is that length based references for saddle height configuration does not take into account particular differences in thigh, shank and foot length. The effectiveness of the “optimum” relationship between bicycle components and body dimensions failed to result in similar body positions because joint angles have not been taken into account. An optimal combination of hip, knee and ankle joint angles would indeed result in optimal power production from the lower limb muscles. In cycling the use of video analysis to optimize the configuration of bicycle components is increasing [7, 8]. However, all guidelines are based on measurements of the cyclist in static poses without information on potentially optimum joint angles from dynamic assessments. Burke and Pruitt [3] suggested that knee flexion angle should be between 25–30° when the pedal is static at the * Corresponding author. 36 bottom of the crank cycle (6 o’clock crank position) for an optimum saddle height configuration. Yet, Peveler et al. [7] showed that the knee flexion angle measured statically at the 6 o’clock crank position underestimated the knee flexion angle taken during cycling motion by ~17%. Their result indicates that another approach should be taken to ascertain the saddle height by using either a dynamical assessment or a static measure in a different crank position (whenever video analysis is not possible). Assuming that the peak crank torque is applied close to the 3 o’clock crank position [9] and that leads to peak patellofemoral compressive force [10], this position could be used rather than the 6 o’clock crank position. Also, the 3 o’clock crank position has been used to ascertain the forward-backward saddle position [11] and that is closer to the knee joint angle of optimal quadriceps muscle force production for cyclists [12]. Given previous studies showed that knee flexion angles are larger at dynamic compared to static assessments of cyclists [7, 8], a comparison between static and dynamic analyses of joint angles for optimization of bicycle components have not fully being explored. This comparison could show that a static position of cyclists (i.e. at 3 o’clock crank angle) could be valid to replicate joint angle observed during cycling motion. Clinicians that do not have access to motion analysis systems could then benefit by using a single digital still camera to capture images from cyclists at a given position on their bicycles. Bicycle saddle position (vertical and fore-aft) could then be configured more properly, leading to an improvement in bike fitting methods. HUMAN MOVEMENT R.R. Bini, P. Hume, Comparison of static and dynamic angles in cycling Thus, the aim of this study was to compare lower limb joint angles of cyclists in static postures compared to dynamic cycling. This comparison would indicate if joint angles taken during static poses at the 3 o’clock crank position would replicate a dynamic cycling motion. The hypothesis was that cyclists would replicate similar joint angles in static poses only at the 3 o’clock crank position. Material and methods Design All cyclists attended one evaluation session (cross-sectional) where anthropometric measures, images from static postures (photogrammetry) and dynamic cycling from video (videogrammetry) from their right sagittal plane were collected. They did not have the configuration of their bicycles changed throughout the study to avoid changing their preferred set up and affect their preferred muscle recruitment. Participants Thirty cyclists with experience ranging from recreational to competitive volunteered to participate in the study. The characteristics of the cyclists were (mean ± SD) 39 ± 10 years old, 80 ± 15 kg body mass, 177 ± 8 cm height, 7.3 ± 3.8 hours/week cycle training, and 8 ± 7 years cycle experience. Prior to the study participants were informed about possible risks and signed a consent form approved by the Ethics Committee of Human Research where the study was conducted in accordance to the declaration of Helsinki. Procedures As landmarks for the hip, knee and ankle joint axes, reflective markers were placed on the right side of the cyclists at the greater trochanter, lateral femoral condyle, and lateral malleolus (see Figure 1). Two markers were attached to the pedal to compute the pedal axis and one marker was attached to the bottom bracket to determine the crank axis. Two markers were taped at a known distance on the bicycle frame for linear image calibration in metric units. The distance from the camera to the bicycle and zoom setting were defined to reduce the motion of the cyclists in the edges of the image frame as an attempt to reduce non-planarity errors in angle computation (for details see Page et al. [13] and Olds and Olive [14]). Cyclists had their own bicycles mounted on a wind trainer (Kingcycle, Buckinghamshire, UK), and were asked to assume a position as similar as possible to outdoors cycling. A digital camera (Samsung ES15, Seoul, South Korea) recorded three high resolution images (3600 × 2400 pixels of resolution) from the sagittal plane with the cyclists standing on the floor (calibration image), cyclists seated on the bicycle with the right crank in the most forward position (3 o’clock) and the right crank in the lowest position on the crank cycle (6 o’clock). One image was recorded at each position to simulate common procedures used in bicycle fitting configuration when a cyclist’s knee flexion angle is measured using a manual goniometer [3, 15]. Cyclists were then asked to select a gear ratio and assume pedalling cadence as similar as possible to steady state cruising road cycling for five minutes simulating regular long distance training. After three minutes of riding, video was recorded for 20 s using the same digital camera (30 Hz, 640 × 480 pixels of resolution) which was shown to provide reliable measurements of rearfoot timing variables (e.g. time of maximal eversion) during running in a previous study [16]. The digital camera used in our study enabled picture capture in high resolution and video recording at regular frame rate and resolution similar to cameras used in motion analysis systems (i.e. 1 mega pixel). Assuming that cyclists would freely choose pedalling cadence close to 90 rpm, we expected that our resolution for crank angle definition would be of 18° per crank revolution and consequently of 3.6° for averages of five crank revolutions. Hip, knee and ankle joint angles were manually digitized from the static postures and video files using ImageJ (National Institute of Health, USA) by the same rater for the 30 cyclists. Joint angles definitions are illustrated in Figure 1. For dynamic cycling, frames taken from five consecutive crank revolutions where cyclists were at the 3 o’clock and at the 6 o’clock crank positions were visually selected to compute joint angles. The average of five revolutions of each joint angle was used for comparison with static poses. The rater’s reliability in digitising was determined using images from static poses analysed on day one and day seven (see results in Table 1). Average pedalling cadence was computed for each cyclist from the time difference taken to cover five consecutive revolutions. Statistical analyses Inferential statistics can be prone to error. Low power of tests would preclude extrapolation of results to a wider population using inferential statistics. Therefore, we used effect sizes opting for a threshold of large effects (ES = 1.0) for substantial changes. This is a more conservative approach than previously described [17], but it would ensure a non-overlapping in distribution of scores greater than 55% [18]. For comparison of measures taken in each image, typical errors were computed as the ratio between the standard deviation from the differences between days and the square root of “2” (TE = SDdiff/√2 – see Hopkins [19] for details). 37 HUMAN MOVEMENT R.R. Bini, P. Hume, Comparison of static and dynamic angles in cycling Cyclists’ means and confidence limits (computed for p < 0.05) were reported for both static and dynamic hip, knee and ankle angles. To compare static and dynamic angles (i.e. hip, knee and ankle), Cohen‘s effect sizes (ES) were computed for the analysis of magnitudes of the differences between the two methods and were rated as trivial (d < 0.25), small (d = 0.25–0.5), moderate (d = 0.5–1.0), and large (d > 1.0) [20]. Mean differences and standard deviation from the differences between the joint angles measured in static and dynamic positions were computed to illustrate the agreement between methods, following description from Bland and Altman [21]. Results Differences in measuring joint angles were trivial between days (< 4.5%) for hip, knee and ankle angles based on analysis of Cohen‘s effect sizes (see Table 1). Within cyclists coefficient of variation of joint angles taken across five crank revolutions was lower than 5%. Errors in determination of the 3 o’clock and the 6 o’clock crank positions in video files were < 1° (< 1%) and 3° (2%), respectively. Freely chosen pedalling cadence was 85 ± 11 rpm for all cyclists. The differences between static and dynamic angles were large at the 6 o’clock crank position with greater hip angle (4.9 ± 1°), smaller knee angle (8.1 ± 2°) and smaller ankle angle (8.5 ± 2°) for static angles. The differences between static and dynamic angles (< 2.5°) were trivial to small for the 3 o’clock crank position (see Figure 1 and Table 2). In Figure 2, we illustrate the mean differences between joint angles measured in static and dynamic positions and the standard deviation from differences for the 6 o’clock and the 3 o’clock crank positions using the Bland–Altman’s plot [21]. Table 1. Intra-rater variability (between days comparison) in the analysis of images from static postures reported as typical error of measurements and effect sizes of the hip, knee and ankle angles at the 6 o’clock and at the 3 o’clock positions of the pedal Between day difference (degrees) Between day difference (%) Typical error (degrees) ES ES – magnitude inference 0.01 0.01 0.13 Trivial Trivial Trivial 0.03 0.01 0.17 Trivial Trivial Trivial 3 o’clock position Hip angle Knee angle Ankle angle 0.03° 0.05° 0.98° 0.61 0.46 4.51 0.14 0.09 1.25 6 o’clock position Hip angle Knee angle Ankle angle 0.05° 0.25° 0.84° 0.48 0.42 4.01 0.12 0.12 0.58 Figure 1. Illustration of reflective marker placement on the right side of the cyclist at the greater trochanter, lateral femoral condyle and lateral malleolus to indicate hip, knee and ankle joint angles. Markers attached to the pedal were used to compute the pedal axis for ankle joint measurement. Mean hip, knee and ankle joint angles are shown for the 30 cyclists for static (S) and dynamic (D) measurements at the 3 o’clock (A) and 6 o’clock (B) crank positions. 38 HUMAN MOVEMENT R.R. Bini, P. Hume, Comparison of static and dynamic angles in cycling Table 2. Hip, knee and ankle angles (mean ± confidence interval – CI) at the 3 o’clock and 6 o’clock crank positions for 30 cyclists. Comparison of the angles determined by static and dynamic methods using effect sizes (ES) Difference between static and dynamic angles Static angle (degrees) Dynamic angle (degrees) Degrees ES ES – magnitude inference 0.1 0.3 0.4 Trivial Trivial Small 1.1 1.5 1.4 Large Large Large 3 o’clock crank position Hip angle Knee angle Ankle angle 38 ± 1.3 62 ± 1.7 125 ± 2.4 38 ± 1.1 63 ± 1.5 122 ± 2.2 0.3 ± 1.1 1.1 ± 1.6 2.5 ± 2.5 6 o’clock crank position Hip angle Knee angle Ankle angle 67 ± 1.8 30 ± 2.4 131 ± 2.1 62 ± 1.4 38 ± 1.5 139 ± 2.4 4.9 ± 1.1 8.1 ± 1.9 8.5 ± 1.9 Figure 2. Differences between measures (individual scores), mean differences between joint angles measured in static and dynamic positions and the standard deviation from differences for the 6 o’clock and the 3 o’clock crank positions using the Bland–Altman’s plot [21] 39 HUMAN MOVEMENT R.R. Bini, P. Hume, Comparison of static and dynamic angles in cycling Discussion In bicycle shops, clinics and bicycle research, configuration of bicycle components to the cyclist (bicycle fitting) takes into account lower limb joint angles determined from a static position of cyclists at the 6 o’clock crank position measured once [3, 11]. However, cycling is a dynamic movement, so bicycle configuration should ideally be based on dynamic assessment looking at the average of consecutive pedal revolutions. Our study reported differences between lower limb joint angles gathered from cyclists in static postures compared to dynamic cycling. Cyclists in our study did not replicate similar angles in static postures as those observed in video analysis when the crank was at the 6 o’clock crank position. Given the fact that the static 6 o’clock crank angle method is commonly used in bicycle shops and clinics, the results of the current study showed that the 3 o’clock position would be a better method to set-up a cyclist on a bicycle if dynamic cycling angles are not available. The measurement of joint angles in images of cyclists on their own bicycles has the potential to improve the existing techniques for bicycle configuration components optimization [15]. Joint angles are important variables for the configuration of bicycle components to help reduce injury risk and optimize performance [6, 22], but the assessment of joint angles of cyclists may depend on exercise conditions. Previous studies presented the dependence of joint angle on workload level [23], pedalling cadence [24], fatigue state [25] and experience in cycling [26]. Therefore, these factors should ideally be taken into account when providing a bicycle set-up. Farrell et al. [27] reported that configuring saddle height to elicit 25–30° of knee flexion using a goniometer with the cyclist in a static pose at the 6 o’clock crank position resulted in 30–45° knee flexion at the same 6 o’clock crank position in video analysis. The larger knee flexion angles (~10°) in dynamic cycling reported by Farrell [27] and Peveler et al. [7] using the goniometer method were also evident in our study (8.2 ± 5°) using the digitisation of the static pose to determine knee flexion angle at the 6 o’clock crank position. Therefore, one has to be careful that the static recommended angles might result in different joint angles than the ones intended for cycling motion. Greater hip angle (smaller flexion), smaller knee angle (smaller flexion) and smaller ankle angle (greater flexion) were observed in static poses at the 6 o’clock crank position compared to the dynamic assessment in our study. Looking at the main driving muscles of cycling (hip and knee joint extensors and ankle plantar flexors), hip and knee joint extensors may be shorter and ankle plantar flexors may be longer in the static pose at the 6 o’clock crank position compared to the one during dynamic cycling due to smaller flexion angles. These differences may affect muscle tendon-unit length and force production [28]. 40 Differences in joint angles between static and dynamic analysis may be related to the lack of angular momentum at the 6 o’clock crank position during static poses, which is contrary to what is observed during dynamic cycling. For pedalling at 90 rpm, cyclists usually present ~27% greater angular velocity of the crank at the 12 o’clock and 6 o’clock crank positions compared to the average angular velocity of the revolution [29]. Two reasons may explain the similarities of the static and dynamic joint angles at the 3 o’clock crank position: 1) There is ~28% lower angular velocity in dynamic cycling at the 3 o’clock crank position than the average angular velocity over the entire revolution of the crank [29]; and 2) To sustain the cranks horizontally at the 3 o’clock crank position, cyclists need to balance the mass of the ipsilateral and contralateral legs. In terms of saddle height adjustment, a range of 25–30° of knee flexion has been recommended to improve efficiency and reduce the risk of injuries in cyclists [22]. Reductions of ~8° may be expected for the knee flexion angle of cyclists assessed statically at the 6 o‘clock position in comparison to dynamic assessment. Therefore setting the saddle height by a static pose of the cyclist taken at the 6 ‘clock position would generally result in a lower saddle height than the one taken dynamically. Depending on the existing saddle height, suboptimal muscle length for force production and increased compressive knee forces would be observed using a lower saddle height [22]. Although the goal of the current study was not to determine recommendations for bicycle fitting, it would be ideal to match the knee flexion angle for optimal torque production (~60–80°, see Folland and Morris [30]) to the one observed at the optimal crank angle for torque production (i.e. 3 o’clock). Future research should be conducted to ascertain on what ranges of hip, knee and ankle angles taken together would optimize cycling performance. The choice of using the same camera to acquire video and capture images of the cyclists in static poses had positive and negative effects in our study. One benefit was that there was no effect from different lenses on image distortion. However, the camera used in the present study was not capable of recording images and video at the same resolution (which would be similar to cameras used by bicycle shops providing bicycle configuration services). Video images had ~19% of the resolution of the static images, which may have reduced the precision of tracking markers in video images compared to images from static poses. However, the choice for analysis of mean results of joint angles over five crank revolutions increased the accuracy of crank angle determination for joint angle computation. Sources of error using sagittal plane video may be out of plane movements and linear image calibration. In cycling, most movement can be assessed via sagittal plane analysis, but up to 10% of differences may be expected for the hip angle when measuring from the HUMAN MOVEMENT R.R. Bini, P. Hume, Comparison of static and dynamic angles in cycling sagittal plane compared to 3D analysis [31]. Pelvic motion during cycling may also affect the comparison of images from static and dynamic analyses. Horizontal (± 5 cm) and vertical (± 2 cm) motion of the hip joint occurs during stationary cycling [32] which may affect lower limb joint angles especially for cyclists using a higher saddle height. Therefore, bicycle set-up should ideally use images from both sagittal and frontal planes or 3D analyses. Conclusions Cyclists did not replicate in a static pose at the 6 o’clock crank position similar hip, knee and ankle joint angles as measured in dynamic cycling. To perform configuration of bicycle components using joint angles, measurements should be taken dynamically or with the cyclists in static poses at the 3 o’clock crank position, instead of the usually recommended 6 o’clock crank position. Acknowledgements The first author acknowledges Capes-Brazil for his PhD scholarship. 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Neptune R.R., Hull M.L., Methods for determining hip movement in seated cycling and their effect on kinematics and kinetics. J Appl Biomech, 1996, 12 (4), 493– 507. Paper received by the Editor: December 31, 2015 Paper accepted for publication: March 18, 2016 Correspondence address Rodrigo Bini Divisão de Pesquisa e Extensão Escola de Educação Física do Exército Centro de Capacitação Física do Exército Av. João Luiz Alves s/n, Urca, Rio de Janeiro, Brazil e-mail: bini.rodrigo@gmail.com 42 HUMAN MOVEMENT 2016, vol. 17 (1), 43– 49 JOINT-ANGLE SPECIFIC STRENGTH ADAPTATIONS INFLUENCE IMPROVEMENTS IN POWER IN HIGHLY TRAINED ATHLETES doi: 10.1515/humo-2016-0006 Matthew R. Rhea1 *, Joseph G. Kenn 2 , Mark D. Peterson 3 , Drew Massey 4 , Roberto Simão 5, Pedro J. Marin 6 , Mike Favero 7, Diogo Cardozo 5, 8 , Darren Krein 9 1 A.T. Still University, Mesa, Arizona, USA Carolina Panthers, National Football League, Charlotte, North Carolina, USA 3 University of Michigan, Ann Arbor, Michigan, USA 4 Game Time Sports and Training, Columbia, Tennessee, USA 5 Rio de Janeiro Federal University, Rio de Janeiro, Brazil 6 CYMO Research Institute, Valladolid, Spain 7 Logan High School, Logan, Utah, USA 8 Granbery Methodist College, Juiz de Fora, Brazil 9 Indianapolis Colts, National Football League, Indianapolis, Indiana, USA 2 Abstract Purpose. The purpose of this study was to examine the influence of training at different ranges of motion during the squat exercise on joint-angle specific strength adaptations. Methods. Twenty eight men were randomly assigned to one of three training groups, differing only in the depth of squats (quarter squat, half squat, and full squat) performed in 16-week training intervention. Strength measures were conducted in the back squat pre-, mid-, and post-training at all three depths. Vertical jump and 40-yard sprint time were also measured. Results. Individuals in the quarter and full squat training groups improved significantly more at the specific depth at which they trained when compared to the other two groups (p < 0.05). Jump height and sprint speed improved in all groups (p < 0.05); however, the quarter squat had the greatest transfer to both outcomes. Conclusions. Consistently including quarter squats in workouts aimed at maximizing speed and jumping power can result in greater improvements. Key words: vertical jump, speed, squat depth, performance enhancement, sports conditioning Introduction The ultimate goal of a sports conditioning program is to enhance each individual athlete’s athletic potential through a structured program of physical development and injury prevention [1]. To this end, specificity of training is a concept that should be of great importance to sports conditioning professionals. The body will adapt in very specific ways to meet the demands of a specific, re-occurring stress [2]. Resistance training that mimics the movements and demands of a given sport may enhance performance in that sport through specific adaptations in neuromuscular performance. Siff [2] detailed this concept in a more complex, neurophysiologic manner stating that “it is vital to remember that all exercise involves information processing in the central nervous and neuromuscular systems, so that all training should be regarded as a way in which the body’s extremely complex computing systems are programmed and applied in the solution of all motor tasks”. It is important to consider how the specific stress applied to an athlete’s body in conditioning will effect * Corresponding author. or stimulate the neuromuscular system, as well as how conditioning can result in improved information processing and physiological performance in specific sport skills. Accordingly, alterations in the range of motion for a given exercise may, theoretically, result in different adaptations. Squat depth has been a topic of much discussion in the field and literature [3–11] with primary focus centering on strength improvements at different training depths. More broadly, this debate is an issue of joint-angle specificity, which has been examined for comparable strength improvements [12–17]. The topic of joint-angle specificity was initially examined with isometric and isokinetic training, which was shown to increase strength at or near the angles trained, and at or near angular velocities trained, with little or no adaptation at other angles/velocities [17]. Three primary squat depths have been characterized and discussed in the literature [18], including partial/ quarter squats (40–60 degree knee angle), parallel/half squats (70–100 degree knee angle), and deep/full squats (greater than 100 degree knee angle). Range of motion variation during the squat exercise influences various biomechanical factors that relate to specificity of movement pattern, and can affect the development of force, rate of force development, activation and synchroniza43 HUMAN MOVEMENT M.R. Rhea et al., Joint-angle specific strength adaptations tion of motor units, and dynamic joint stability. Therefore, the manner in which an exercise changes based on range of motion is an important concept to examine. The purpose of this study was to examine the influence of training at different squat depths on jointangle specific strength as well as transfer to several sportsrelated performance variables. Understanding the effects of training at different ranges of motion can help the strength and conditioning professional to apply the most effective training strategy and further the performance enhancement advantages of evidence-based training prescriptions. Material and methods Subjects Male college athletes of all sports at various schools (Division I, II, III and Junior College) were invited to participate in this research. Inclusion criteria included: 1) minimum of 2 years of consistent year-round training, 2) a minimum parallel squat 1RM of at least 1.5 times body weight, and 3) no physical condition that would impair aggressive sports conditioning and high-intense resistance training. A total of 38 athletes volunteered to participate. Of those, 32 met the minimum strength requirement. Two subjects experiencing tendonitis in the knee were excluded prior to group assignment. Two subjects withdrew during the initial testing period, resulting in 28 total subjects entering the training portion of the study. The methods and procedures for this study were evaluated and approved by an Institutional Review Board for research with Human Subjects and all participants provided informed consent. The majority (n = 24) of the subjects were football players, with track (n = 1), basketball (n = 2), and wrestling (n = 1) completing the sport backgrounds. Random assignment resulted in 3 groups with similar anthropometric measures, strength, and training experience. Descriptive data are presented in Table 1. Procedures Trained staff familiar with proper testing procedures and data handling performed all testing. Those conducting the pre-, mid-, and post-tests were blinded to the group assignment of each subject to avoid any potential bias. Experienced coaches implemented and over- saw the training program to ensure proper execution, tempo, and adherence to the prescribed program. Strength testing was performed in accordance with published guidelines of National Strength and Conditioning Association [19]. Subjects performed one repetition maximum (1RM) testing at each of the three squat depths (quarter, half, and full) in three separate sessions, randomized in order, with a minimum of 72 hours between testing sessions. All 1RM values were achieved within 3 attempts. In a fourth and final testing session designed to examine the reliability of the strength data, each subject repeated the 1RM testing procedures for each depth (Intraclass Correlation Coefficient ranging from 0.95–0.98). Non-significant differences (p > 0.05) were found between 1RM values on the different testing days at each specific depth tested; however, the highest 1RM for each depth was utilized for data analysis. Testing at week 8 was performed in a 7-day period with each depth randomly tested on a separate day a minimum of 48 hours apart. Post-intervention testing was performed according to the same protocols explained for the pre-testing. Vertical jump testing was performed according to protocols previously published [19]. Immediately following the dynamic warm-up in the first two testing sessions, all subjects were tested for their vertical jump using the Vertec (Vertec Sports Imports, Hilliard, OH). Subjects were given 3 attempts with the maximum height recorded. Non-significant differences were found between the two testing sessions (p > 0.05) but the highest jump height was recorded for data analysis. Sprint testing was performed according to protocols previously published [19]. Following the dynamic warmup in the first two testing sessions, all subjects performed a 40-yard sprint test. Electronic timing for the sprint was conducted with a wireless timing system (Brower Timing Systems, Draper, Utah). Subjects were given 2 attempts in each session with the maximum speed recorded. Non-significant differences were found between the two testing sessions (p > 0.05) but the fastest speed was recorded for data analysis. All aspects of the training program were identical for each group with the exception of squat depth and absolute load. Within subject strength differences at each depth, due to the biomechanical disadvantage with increased depth, resulted in greater absolute loads being used at quarter and half squat depths. However, relative loads were the same for each group. The program Table 1. Baseline Descriptive Data Group Age (years) Weight (kg) Pre-Quarter 1RM (kg) Pre-Half 1RM (kg) Pre-Full 1RM (kg) Pre-VJ (cm) Pre-40 (sec) QTR HALF FULL 21.4 (3.2) 20.7 (2.1) 21.3 (1.3) 86.5 (25.6) 95.7 (32.1) 92.1 (23.8) 167.67 (13.95) 162.12 (12.22) 164.09 (13.18) 151.51 (15.12) 146.72 (11.54) 151.82 (12.80) 129.54 (17.23) 125.50 (14.09) 125.91 (18.38) 75.92 (15.06) 77.03 (11.05) 73.91 (14,25) 4.68 (0.18) 4.73 (0.18) 4.76 (0.20) 1RM – 1 repetition maximum, VJ – vertical jump, 40 – 40 yard sprint 44 HUMAN MOVEMENT M.R. Rhea et al., Joint-angle specific strength adaptations followed a daily undulating periodization sequence with intensity progressing from 8RM, 6RM, 4RM, to 2RM then reverting back to 8RM. Training weight was estimated using 1RM prediction equations based on the 1RM measures at the specific depth of training group, with notations made for rep ranges in each workout that required adjustments to the predicted values. A split training routine was implemented to enable greater monitoring and control of lower body exercises. Lower body exercises (squats, power cleans, lunges, reverse hamstring curls, and step ups) were performed on Monday and Thursday, and upper body exercises performed on Tuesday and Friday. Squats (65%) and power cleans (25%) made up 90% of the training volume for the lower body with the other exercises added for general athletic preparation but at low volumes in each session (1–3 sets) and were identical for all three groups. Exercise order was kept constant for all groups and subjects. Wednesday, Saturday, and Sunday were designated as rest days with no exercise prescribed or allowed. Lower body workouts included 4–8 sets of squats, at the prescribed depth, followed by each of the other exercises. A linear periodization adjustment in volume was made throughout the training program (weeks 1–2: 8 sets; weeks 3–4: 6 sets; weeks 5–6: 4 sets; weeks 7–10: 8 sets; weeks 11–14: 6 sets; weeks 15–16: 4 sets). A threeminute rest was provided between each set. This resulted in total volume, relative intensity, and workout sessions that were equated across the 16-week training intervention for all groups. Squat depth was taught and monitored via videotaping throughout the training program. The first group performed full squats (FULL) with range of motion determined by the top of the thigh crossing below parallel to the floor and knee angles exceeding 110 degrees of flexion. The half squat group (HALF) trained at depths characterized by the top of the thigh reaching parallel to the floor with knee angles approximately 85–95 degrees of flexion. The final group performed quarter squats (QTR) with range of motion involving a squat to approximately 55–65 degrees of knee flexion. During the initial sessions, and during all testing, a goniometer (Orthopedic Equipment Company, Bourbon, Indiana) was used to measure the appropriate depth. Safety bars were raised or lowered in the squat rack for each subject to provide a visual gauge of the depth required. The coach provided immediate feedback if a slight alteration in depth was needed within a set. A minimum of 30 workouts (out of 32) was required to be included in the final data analysis. This ensured that all subjects included in the analysis had completed roughly the same amount of work throughout the program. All 28 subjects met this requirement. Statistical analyses Data were analyzed using PASW/SPSS Statistics 20.0 (SPSS Inc, Chicago, IL, USA). The normality of the data was checked and subsequently confirmed with the Shapiro–Wilk test. Dependent variables were evaluated with a repeated measures analysis of variance (ANOVA) on group (QTR; HALF; FULL) × time (Baseline; Mid; Post). When a significant F-value was achieved, pairwise comparisons were performed using the Bonferroni post hoc procedure. The level of significance was fixed at p 0.05. Partial Eta squared statistics ( 2) were analyzed to determine the magnitude of an effect independent of sample size. Pre/Post effect sizes were calculated for each group and performance measure [20]. The coefficient of the transfer was then calculated from squat result gains to vertical jump and sprinting speed via a calculation reported by Zatsiorsky [21]: Transfer = Result Gain in nontrained exercise/Result Gain in trained exercise Result Gain = Gain in performance/Standard deviation of performance The associations between different measures were assessed by Pearson product moment correlation at baseline time. Values are expressed as mean ± SD in the text, and as mean ± SE in the figures. Results Quarter squat – 1RM-test A group × time interaction effect was noted for quarter squat test (p = 0.002; 2 = 0.545; see Figure 1a). A main effect of the group was observed (p < 0.001; 2 = 0.652), as well as a main effect of the time was noted (p = 0.012; 2 = 0.322). Half squat – 1RM-test A group × time interaction effect was noted for half squat test (p < 0.001; 2 = 0.563; see Figure 1b). However, there was no significant a main effect of the group was observed (p > 0.05; 2 = 0.002). A main effect of the time was noted (p < 0.001; 2 = 0.930). Full squat – 1RM-test A group × time interaction effect was noted for full squat test (p < 0.001; 2 = 0.647; see Figure 1c). However, there was no significant a main effect of the group was observed (p = 0.074; 2 = 0.278). A main effect of the time was noted (p < 0.001; 2 = 0.623). Vertical Jump Test A group × time interaction effect was noted for vertical jump test (p < 0.001; 2 = 0.689; see Figure 2). However, there was no significant a main effect of the group was observed (p > 0.05; 2 = 0.146). A main effect of the time was noted (p < 0.001; 2 = 0.795). 45 HUMAN MOVEMENT M.R. Rhea et al., Joint-angle specific strength adaptations Sprint Test A group × time interaction effect was noted for vertical jump test (p < 0.001; 2 = 0.615; see Figure 3). However, no significant main effect of the group was observed (p > 0.05; 2 = 0.232). A main effect of the time was noted (p < 0.001; 2 = 0.836). Percent change (Table 2) and effect size calculations (Table 3) demonstrated the greatest changes in strength at the specific depth at which each group trained. QTR squat improved 12% in the quarter squat 1RM, HALF 14% at half 1RM, and FULL improved 17% in the full squat 1RM. For VJ and 40-sprint, the QTR squat group showed the greatest treatment effect (VJ: 0.75; Sprin: –0.58), followed by HALF (VJ: 0.48; Sprint: –0.35), with FULL showing the lowest magnitude of training effect (VJ: 0.07; Sprint: –0.10). Transfer calculations (Table 4) somewhat mimicked the other trends in the data with QTR showing the greatest transfer to VJ (0.53), with HALF next (0.28), and FULL showing the least amount of transfer (0.06). For sprinting speed, QTR showed the greatest transfe (–0.41) with HALF second (–0.20) and FUL (–0.09) again showing the least transfer. Finally, correlation analysis (Table 5) demonstrated stronger relationships between the QTR squat group and both VJ (r = 0.64) and Sprint (r = –0.74) performances followed by HALF (r = 0.43 and r = –0.57) and FULL (r = 0.31 and r = –0.49). Discussion Taken collectively, these findings support the use of shortened ranges of motion during squat training for improvements in sprint and jump performance among highly trained college athletes. This conclusion should stimulate further consideration among strength and con- *significantly different from Baseline (p < 0.05) # significantly different from Mid (week 8) (p < 0.05) † significantly different compared with the QTR group (p < 0.05) Figure 2. Vertical Jump Test. Values are mean ± SE (QTR Group, n = 9; HALF Group, n = 9; FULL Group, n = 10) *significantly different from Baseline (p < 0.05) # significantly different from Mid (week 8) (p < 0.05) † significantly different compared with the QTR group (p < 0.05) ‡ significantly different compared with the HALF group (p < 0.05) Figure 1. Squat tests. Values are mean ± SE (QTR Group, n = 9; HALF Group, n = 9; FULL Group, n = 10) 46 * significantly different from Baseline (p < 0.05) # significantly different from Mid (week 8) (p < 0.05) † significantly different compared with the QTR group (p < 0.05) Figure 3. Sprint test. Values are mean ± SE (QTR Group, n = 9; HALF Group, n = 9; FULL Group, n = 10) HUMAN MOVEMENT M.R. Rhea et al., Joint-angle specific strength adaptations Table 2. Percet changes in performane measures Group Quarter Squat Half Squat Full Squat VJ 40 sprint QTR HALF FULL 0.12 0.07 0.00 0.06 0.14 0.05 0.02 0.00 0.17 0.15 0.07 0.01 –0.02 –0.01 0.00 VJ – vertical jump; 40 – 40 yard sprint Table 3. Effect size calculations based on squat depth Group Quarter 1RM Half 1RM Full 1RM VJ 40 sprint QTR HALF FULL 1.41 0.88 0.05 0.62 1.76 0.59 0.12 0.02 1.14 0.75 0.48 0.07 –0.58 –0.35 –0.10 ES – (post-pre)/pre-test SD Table 4. Coefficient of transfer calculations Group QTR HALF FULL Quarter 1RM Half 1RM Full 1RM VJ 40 sprint 1.00 0.51 0.05 0.44 1.00 0.52 0.08 0.01 1.00 0.53 0.28 0.06 –0.41 –0.20 –0.09 coefficient of transfer – result gain in nontrained exercise/result gain in trained exercise Table 5. Bivariate correlations between strength capacities at different squat depths, vertical jump height, and sprint speed (n = 28) Group Quarter 1RM Half 1RM Full 1RM VJ 40 sprint Quarter 1RM Half 1RM 1 0.847** 0.847** 1 0.722** 0.693** 0.640** 0.428* –0.740** –0.567** Full 1RM 0.722** 0.693** 1 0.309 –0.490** VJ –0.640** 0.428* 0.309 1 –0.779** Sprint 0.740** –0.567** –0.490** –0.779** 1 ** correlation is significant at the 0.01 (2-tailed) ditioning coaches regarding the use of quarter squats in a sports conditioning program. Further examination of the risks, benefits, and implementation of squats of various depths is warranted, and will be discussed here. Weiss et al. [7] conducted a study examining deep and shallow squat (corresponding to half and quarter squats in our study) and leg press training on vertical jump among untrained college students. Their study failed to find any significant changes in vertical jump for either group regardless of squat depth but two transfer calculations suggested greater transfer from the half squat training program to vertical jump. They did find statistically significant improvements in 1RM squat at the angle of training. The half squat group also improved 1RM at the quarter squat depth; however, the quarter squat training group did not improve 1RM performance in the half squat test. Our findings concur with the joint-angle specific improvement in strength relative to the angle where training occurred but differ in that our study did not show an improvement in quarter squats in the half or full squat training groups. Additionally, we found far less transfer from deep squat training to vertical jump. Several distinct differences exist between these two studies, perhaps accounting for the different findings. Our study utilized very highly trained athletes training with free weights instead of untrained college students who trained with machines. Our study was also nearly twice the length (16 weeks compared to 9 weeks). It is notable that in our study, the mid-test data (8 weeks) showed no significant findings, highlighting the need for longer studies to examine these important training issues more critically. It is also possible that as an individual becomes more highly trained, jointangle specific adaptations are more pronounced and detectable. Joint-angle specificity has been suggested to relate to neurological control [17]. Thepaut-Mathieu et al. [14] found increases in EMG activity at trained joint angles 47 HUMAN MOVEMENT M.R. Rhea et al., Joint-angle specific strength adaptations compared to untrained joint angles suggesting an increase in neural drive at the specific angles trained. Those data highlight the complexity of the nervous system processes for gathering information and responding to motor challenges. It appears that the nervous system gathers information relative to joint angles, contraction type, and angular velocities during training, responding with adaptations specific to those training demands. An examination of the differences in squat 1RM at the three different depths in the current study provides valuable information relative to joint-angle specific loads and may assist in the development of an explanation of why quarter squats transfer more to jumping and sprinting speed. First, the quarter squat range of motion matches more closely the hip and knee flexion ranges observed in jumping and sprinting. That said, on average, athletes were able to squat 30–45% more in a quarter squat compared to the full squat depth (10–20% more when compared to half squat depth). Using 1RM testing at full squat depths to calculate and apply training loads through a full squat range of motion, results in training loads at the top of the range of motion representing less than 70% of maximum lifting capacity in that range of motion. Consistently training at 60–80% of maximum capacity may promote strength gains in less trained populations but would not be considered sufficient for optimal strength development among more highly trained populations [22]. Quarter squats would not be expected to improve full squat strength due to the lack of stress applied in full squat joint angles and the data in the current study supports that assertion. But the load during full squats appears to be insufficient to promote significant gains in strength in the quarter squat joint angles in highly trained populations. Thus, the loads that are calculated for training are specific to the joint angles at, or near, the angle at which testing occurs. They do not represent optimal training loads for all angles in the range of motion. Isometric research [15] has shown that strength improvements only occur at or near the joint-angles where training occurs. Our data support this concept, as all of our groups were similar in gains at the half squat depth; however, significant differences were found at quarter and deep squats based on the training depths. The concept of joint-angle specificity as it relates to resistance training has generally been described as improvements in function at the joint-angles where training occurs. Under this philosophy, conventional thought has suggested that athletes must train through a full range of motion to ensure adaptations at all joint-angles. Given the data of the current study, it seems that strength improvements are specific to joint-angles that are sufficiently overloaded, not just joint-angles where training occurs. Therefore, we propose a change in perspective, based on the current data and theory, to reflect the concept of joint-angle overload. It is suggested that improvements in muscular fitness will occur at the joint-angles that are sufficiently 48 overloaded by the load placed upon them. In the conventional approach to measuring 1RM values at either a parallel or deep squat depth, and then performing squats at a certain percentage of that 1RM through a parallel or deep squat range of motion, the joint-angles involved in jumping and sprinting may not be sufficiently overloaded for maximal gains. Returning to the concepts proposed by Siff [2] regarding information processing during training, it is suggested that the neuromuscular system perceives, and adapts to, stresses applied during quarter squats much differently than full squats. It is also important that the strength and conditioning professional differentiate between transfer and value. If the goal of a specific workout were to enhance sprinting or jumping, quarter squats would be the most effective range of motion based on the current data. But other squat depths may have value in preparing the athlete for competition, and coaches should examine the benefits, and risks, associated with squats of varying depths. If or when value exists, regardless of the amount of transfer directly to a given sports skill, an exercise or range of motion should be used to ensure that the athlete gains the full value of that exercise. Different EMG activation patterns have been shown with various squat depths [10] and may provide evidence of specific value outside of transfer to sport skills. Full squats were shown to result in greater gluteus maximus activation with decreased hamstring involvement. Thus, squat depth may preferentially target recruitment of different muscle groups. Understanding the exact benefits or drawbacks of different exercises and ranges of motion is imperative to optimal training and strength and conditioning professionals should place high value on educating themselves and their clients regarding the pros and cons of a certain exercise or range of motion. An additional consideration when selecting squat variations is the different stresses that each variation presents to the athlete. Schoenfeld [18] provides a detailed review of the various stresses that occur at the ankle, knee, and hip joints during the squat exercise at various depths. With changing loads and ranges of motion, stress appears to vary substantially. The increased load in a quarter squat, combined with the increased anterior shear force in that range, could present added risk of overuse injury if athletes only performed quarter squats. The same could be said of all squat depths and the best approach for health and performance enhancement may be to include different squat variations (i.e. back, front, split) at all three squat depths. Squats of different depths may need to be considered as separate exercises, or tools, employed for various purposes or to target specific muscles. A mixture of different squat depths, much like the use of various different exercises throughout a training program, may be the optimal approach to developing the total athlete. However, based on the data from this study, it is clear that the use of quarter squats is not only helpful, but also necessary for promoting maximal sprinting and jumping capabilities. HUMAN MOVEMENT M.R. Rhea et al., Joint-angle specific strength adaptations Conclusions In summary given the significantly greater transfer to improvements in sprinting and jumping ability, the use of quarter squats during sports conditioning is recommended. Including quarter squats in workouts aimed at maximizing speed and jumping power can result in greater improvements in sport skills. While squats through a full range of motion may be useful in a general sports conditioning regimen, strength and conditioning professionals should consider the integration of quarter squats for maximizing sprinting and jumping ability. References 1. Kenn J., The coach’s strength training playbook. Coaches Choice, Monterey 2003. 2. Siff M.C., Supertraining. Supertraining Institute, Denver, Colorado 2003. 3. Chandler T.J., Wilson G.D., Stone M.H., The squat exercise: attitudes and practices of high school football coaches. Natl Strength Cond Assoc J, 1989, 11 (1), 30–36. 4. Chandler T.J., Wilson G.D., Stone M.H., The effect of the squat exercise on knee stability. Med Sci Sports Exerc, 1989, 21 (3), 299–303. Available from: http://journals. lww.com/acsm-msse/pages/articleviewer.aspx?year=19 89&issue=06000&article=00012&type=abstract 5. Klein K.K., The deep squat exercise as utilized in weight training for athletes and its effects on the ligaments of the knee. JAPMR, 1961, 15 (1), 6–11. 6. Wilson G.J., Newton R.U., Murphy A.J., Humphries B.J., The optimal training load for the development of dynamic athletic performance. Med Sci Sports Exerc, 1993, 25 (11), 1279–1286. Available from: ournals.lww.com/acsm-msse/ pages/articleviewer.aspx?year=1993&issue=11000&art icle=00013&type=abstract. 7. Weiss L.W., Frx A.C., Wood L.E., Relyea G.E., Melton C., Comparative effects of deep versus shallow squat and legpress training on vertical jumping ability and related factors. J Strength Cond Res, 2000, 14 (3), 241–247. 8. Escamilla R.F., Knee biomechanics of the dynamic squat exercise. Med Sci Sports Exerc, 2001, 33 (1), 127–141. Available from: http://journals.lww.com/acsm-msse/pages/ articleviewer.aspx?year=2001&issue=01000&article= 00020&type=abstract. 9. Rogers L., Sherman T., Leg press versus squat. 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Rhea M.R., Determining the magnitude of treatment effects in strength training research through the use of the effect size. J Strength Cond Res, 2004, 18 (4), 918–920. 21. Zatsiorsky V.M., Science and practice of strength training. Human Kinetics, Champaign 1995. 22. Rhea M.R., Alvar B.A., Burkett L.N., Ball S.D., A metaanalysis to determine the dose response for strength development. Med Sci Sports Exerc, 2003, 35 (3), 456–464, doi: 10.1249/01.MSS.0000053727.63505.D4. Paper received by the Editor: September 22, 2015 Paper accepted for publication: March 21, 2016 Correspondence address Matthew Rhea Kinesiology Department A.T. Still University 5850 East Still Circle, Mesa AZ 85206, USA e-mail: mrhea@atsu.edu 49 HUMAN MOVEMENT 2016, vol. 17 (1), 50– 55 ANAEROBIC EXERCISE AFFECTS THE SALIVA ANTIOXIDANT/OXIDANT BALANCE IN HIGH-PERFORMANCE PENTATHLON ATHLETES doi: 10.1515/humo-2016-0003 Marcelo de Lima Sant’Anna1, 2 , Gustavo Casimiro-Lopes 1, 3 , Gabriel Boaventura1, 3 , Sergio Tadeu Farinha Marques 4 , Martha Meriwether Sorenson 1, Roberto Simão 1, Verônica Salerno Pinto 1 * 1 Department of Biosciences Physical Activity, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil Instruction Center Almirante Sylvio de Camargo, Rio de Janeiro, Brazil 3 Institute of Medical Biochemistry, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil 4 Navy Sports Commission, Rio de Janeiro, Brazil 2 Abstract Purpose. Investigate free radical production and antioxidant buffering in military pentathletes’ saliva after their performance of a standardized, running-based anaerobic sprint test (RAST). Methods. Seven members of the Brazilian Navy pentathlon team were recruited to perform a running-based anaerobic test (~90 sec). The participants provided samples of saliva before and after the test that were analyzed for biomarkers of oxidative stress such as lipid peroxidation, total antioxidant capacity and the quantity of two specific antioxidants, glutathione and uric acid. Results. The lipid peroxidation increased ~2 fold after RAST, despite an increase in total antioxidant capacity (46%). The concentration of reduced glutathione did not change, while the uric acid concentration increased by 65%. Conclusions. The evaluation in saliva following a sprint test that lasted no more than 90 sec was sensitive enough to reveal changes in redox state. Key words: saliva, physical exercise, oxidative stress, GSH, lipid peroxidation Introduction Free radicals are not intrinsically harmful to health: low-to-moderate concentrations play multiple regulatory roles in gene expression, cell signaling, and skeletal muscle force production [1, 2]. However, if there is an imbalance between production of free radicals and antioxidant capacity, oxidative stress occurs and can provoke tissue damage [3, 4]. Anaerobic and aerobic exercise can both increase free radical formation. Prominent among mechanisms of free radical production during anaerobic exercise are mitochondrial leakage, ischemia-reperfusion response and leukocyte activation [5, 6], so a short burst of intense anaerobic exercise can be effective in generating oxidative stress as assessed by xanthine oxidase activity and markers for lipid peroxidation, protein carbonylation, and DNA oxidation, as well as total antioxidant capacity [5]. Strenuous aerobic exercise induces an increase in lipid peroxidation in human plasma [1], likely generated by hydroxyl radical attack on polyunsaturated fatty acids [5]. Providing blood samples increases stress in athletes that can limit their willingness to participate in scientific studies, especially during competition. This study examines oxidative stress, for the first time in military * Corresponding author. 50 athletes training for an international competition called the naval pentathlon, using a non-invasive analysis of saliva. The naval pentathlon consists of five different tests performed on consecutive days. The tasks require intense anaerobic effort and in some cases apnea. There is very little published about reactive oxygen species (ROS)/ antioxidant balance in saliva of high-level anaerobic athletes. We hypothesized that saliva samples are suitable as biological material to monitor changes in biomarkers for free radical generation and total antioxidant capacity. Saliva samples were collected before and after a short test, RAST (running-based anaerobic sprint test), and used to assess anaerobic performance during the training period [7]. Material and methods Subjects Subjects were seven military athletes of the Brazilian Navy, all of them experienced in international competition in naval pentathlon. They were engaged in the final weeks of training for a series of international tournaments. The team with five men and two women volunteered to participate in the study. Their written informed consents were obtained after explanation of the purpose, benefits and potential risks to the subjects. All military personnel are submitted to periodic medical and odontological examinations. The results of the oral health evaluation were used to exclude any athletes HUMAN MOVEMENT M. de Lima Sant’Anna et al., Redox balance in athlete’s saliva showing symptoms of oral inflammation, periodontitis or gingivitis. The diet of all participants during the week prior to testing was the same and obtained from the military facility, which was controlled by a military nutricionist to meet the energy demands of the armed services. Subjects were instructed not to ingest supplemental vitamins or antioxidants. In addition, each was instructed to avoid smoke and heavy physical exercise for 1h prior to testing. The experimental protocol was approved by the Ethics Committee of Clementino Fraga Filho Hospital of the Federal University of Rio de Janeiro. Aerobic capacity and anthropometric measurements Maximal oxygen consumption (VO2max) was estimated on a synthetic outdoor track several days before the RAST, applying the distance run in 12 min to the Cooper [8] regression equation. The results are presented in relative rate in milliliters of oxygen per kilogram of body weight per minute (Table 1). Skinfold thickness was measured as described in Pollock and Jackson [9]. Body fat percentage was determined using the Siri [10] equation. Exercise test The RAST, a single set applied individually, was performed outdoors on grass. It consisted of 5 min of very light warm-up (stretching and jogging) followed by 6 × 35-m sprints as fast as possible, with 10 s between sprints, and the last sprint followed by 5 min of cool-down. The power generated in each sprint was calculated by the formula Power (W) = (Body mass × Distance2)/Time3, normalized to body weight (Table 2). Table 1. Anthropometric characteristics and aerobic capacity Age (yr) Body mass (kg) Height (cm) BMI* (kg/m2) Body fat (%) VO2max (mL/kg · min) Mean ± SD Range 27.1 ± 5.4 65.3 ± 6.6 170 ± 10 21.9 ± 0.8 10.2 ± 5.6 61.9 ± 12.0 21–31 53.8–72.2 160–185 20.7–23.2 3.9–20.3 44.6–73.7 * body mass index = mass(kg)/(height(m))2 Table 2. Measures of performance in the RAST Mean ± SD Peak power per weight (W/kg) 6.5 ± 1.4 Average power per weight (W/kg) 5.4 ± 1.1 Minimum power per weight (W/kg) 4.6 ± 1.1 Range 4.4–7.9 3.8–6.7 3.0–5.9 Collection of saliva To avoid contamination, the subjects washed their mouths with deionized water before the collection and then chewed a piece of cotton wool for 1 min. Saliva samples were collected before and 5 min after the RAST as suggested by several papers [11–13]. After being collected, the samples were transported on ice to the laboratory and centrifuged at 3,000 × g for 10 min at 4°C. Supernatants were separated from pellets and stored at – 20°C. Lipid peroxidation assay The lipid peroxidation assay was performed as described by Zalavras et al. [14] with slight modification. One hundred microliters of saliva supernatant was mixed with 500 µL TCA (35%, w/v) and 500 µL Tris-HCl (200 mM, pH 7.4) and incubated for 10 min at room temperature. One milliliter of a solution containing 55 mM thiobarbituric acid in 2 M Na2SO4 was added and the samples were incubated at 95°C for 45 min and then cooled on ice for 5 min. After the addition of 1 mL TCA (70%, w/v) they were vortexed and centrifuged at 15,000 × g for 3 min. The absorbance of the supernatant was read at 530 nm and TBARS concentration was calculated using an extinction coefficient of e = 0.156 µM –1 · cm–1. Values were expressed in µM. Total antioxidant capacity The total antioxidant capacity was measured as in Georgakouli et al. [15], using 20 µL saliva, 480 µL sodium-potassium phosphate (10 mM, pH 7.4) and 500 µL 2,2-diphenyl-1-picrylhydrazyl (DPPH, 0.1 mM), incubated in the dark for 30 min and centrifuged for 3 min at 20,000 × g. The absorbance Ac was read at 520 nm and compared with A0, absorbance of a reference sample containing only 20 µL water, DPPH and buffer. Percentage reduction of the DPPH (Q) was defined by Q = 100(A0 – Ac)/A0 [16]. Determination of GSH in saliva One hundred microliters of saliva was added to 200 µL of a 10% solution of TCA, vortexed and centrifuged at 4,000 × g for 10 min at 10°C. To 200 µL of the supernatant was added 700 µL of 400 mM Tris-HCl buffer, pH 8.9, followed by 100 µL of 2.5 mM DTNB dissolved in 40 mM Tris-HCl buffer, pH 8.9. The samples were incubated for 10 min at room temperature and the absorbance was measured at 412 nm. Blanks contained water instead of saliva. The concentration of GSH in the samples was read from a GSH standard curve (0.8 µM – 4 µM) [17]. Power (in watts) is normalized to body weight (kg). 51 HUMAN MOVEMENT M. de Lima Sant’Anna et al., Redox balance in athlete’s saliva Uric acid in saliva 2.5 Statistical analysis Pre- and post-test samples were compared using Student’s paired t-test. Data normality was verified with the Shapiro-Wilk test, which showed that non-parametric test was not required. The power of the performed tests with an = 0.05 was 1.000 to TBARS, 0.735 to DPPH, 0.999 to uric acid and 0.098 to GSH. Correlation between variables were assessed by Pearson’s correlation coefficient. For all analyses, statistical significance was indicated when p < 0.05. Standard errors are reported, except for anthropometric characteristics, aerobic capacity and measures of performance in the RAST. Results 1.5 1.0 0.5 0.0 PRE The subjects showed a high VO2max, as presented in Table 1. Anaerobic power was assessed during each RAST sprint (Table 2). The correlation coefficient between peak anaerobic power and previously determined VO2max for each subject was high (r = 0.94, Figure 1). Lipid peroxidation in saliva In this study the peroxidation of fatty acids was assessed by an assay for thiobarbituric acid-reactive substances (TBARS). After the RAST, the lipid peroxidation was ~2 times higher than at rest (Figure 2). In 90 Figure 2. The anaerobic test RAST induces oxidative stress. Mean ± S.E. (n = 7), *p < 0.05 the pre-test condition the value obtained was 0.9 µM ± 0.2 µM and five minutes after six sprints the value was 1.9 µM ± 0.2 µM. To evaluate the overall antioxidant response to the RAST, which as shown above generated a substantial lipid oxidation, we measured the quenching of DPPH absorbance after the addition of saliva. This measure of total antioxidant capacity increased by 46.6% (Figure 3). Non-enzymatic antioxidant system To evaluate the contribution of the non-enzymatic antioxidant system to the increment observed in total antioxidant capacity, we evaluated the salivary glutathione and uric acid. There was no significant change in glutathione status (Figure 4A), but uric acid increased by 65.6%, from 178.9 µM ± 21.4 µM to 293.5 µM ± 9.4 µM (Figure 4B). 80 10 * 70 8 % QUENCH IN DPPH 60 50 40 30 4 5 6 7 8 POST Total antioxidant capacity Correlation between aerobic and anaerobic performance VO2max (mL/kg.min) * 2.0 TBARS (µM) Urate concentration in saliva was analyzed by a uric acid assay kit (Doles Urato 160, Goiania, GO, Brazil) based on the amount of H2O2 produced when urate is converted to allantoin by uricase. 9 6 4 2 Peak power per kg (W/kg) Figure 1. Correlation between aerobic and anaerobic power for each athlete presented a R2 = 0.8885 and a correlation coefficient of 0.94 (n = 7), p < 0.05 52 0 PRE POST Figure 3. RAST increases the total antioxidant capacity in athletes’ saliva. Mean ± S.E. (n = 7), *p < 0.05 HUMAN MOVEMENT M. de Lima Sant’Anna et al., Redox balance in athlete’s saliva a 50 GSH (µM) 40 30 20 10 0 b PRE POST 350 * 300 URIC ACID (µM) 250 200 150 100 50 0 PRE POST Figure 4. Antioxidant biomarkers. A) Glutathione (GSH); B) Uric acid. Mean ± S.E. (n = 7), *p < 0.05 Discussion The aim of this study was to investigate free radical production and antioxidant buffering in military pentathletes’ saliva after an anaerobic test, RAST. The running-based anaerobic sprint test is designed to assess anaerobic power in sports that mostly use running [7]. The athletes evaluated had a high VO2max, commonly accepted as a key indicator of the endurance capacity. The two women averaged 45.0 ± 0.5 mL/kg · min and the men 69.0 ± 4.0 mL/kg · min. The values for the men were equivalent to those reported for male triathletes (67.6 ± 4.5 mL/kg · min) [18] and a European team of naval pentathlon athletes (74.0 mL/kg · min) [19]. The naval pentathlon is an intense sequence of five anaerobic tasks performed on consecutive days: obstacle race, life-saving swimming race, utility swimming race, seamanship race and amphibious cross-country race. They range from about 60 s (life-saving race) to 10–12 min (cross-country race). The RAST is an intense anaerobic test but it is short and the effort level is lower than the actual naval pentathlon competition. Other authors have studied metabolic parameters after application of a modified RAST protocol, but they did not meas- ure redox status [20]. The RAST has not been exploited for assessment of biochemical changes in athletes, although it is frequently used to predict running performance, with high correlations for 35, 50, 100, 200 and 400 meters [7]. During a pentathlon competition the distance covered by running varies in different tests from 280 to 900 meters. Although the RAST is shorter it was able to provide a measure of pro-oxidant and antioxidant status in well-trained athletes in a controlled test condition. In an intermittent high-intensity test such as the RAST, major sources for ATP replacement are initially phosphocreatine hydrolysis and glycolysis, but a shift toward oxidative metabolism to replenish ATP has been demonstrated for later trials in a sequence of sprints [21]. We observed a high correlation between VO2max and anaerobic power, consistent with a role for aerobic power in anaerobic performance, and suggesting the importance of such a shift during the RAST, as observed for other anaerobically trained athletes, for example, judo players performing an anaerobic judo test that lasted 60 s [22]. Very few studies have proposed saliva as an alternative source to evaluate oxidative stress biomarkers and antioxidant adaptation induced by exercise [11], and Deminice et al. [12] emphasized the differences between redox profiles of plasma and saliva. However, the main finding in our study was that saliva of trained athletes, following an anaerobic test, reveals an increase in lipid peroxidation (TBARS) and at the same time an increase in the antioxidant capacity that can be attributed primarily to uric acid (UA) – consistent with published data obtained using serum or plasma. Under hydroxyl radical attack the double bonds in polyunsatured fatty acid of biological membranes can degrade membrane structure with loss in physiological function and cellular disruption [2, 23]. The increase in lipid peroxidation after six sprints shows that mechanism for free radical production can override antioxidant defenses even in highly trained athletes, and this can be seen clearly in saliva. After the RAST, the quenching of DPPH, a measure of total antioxidant capacity, was 46% higher than at rest (Figure 3). These data show that although these athletes undergo substantial lipid peroxidation (Figure 2), the total antioxidant capacity was not used up. Wayner et al. [24] have assigned total peroxyl trapping in human plasma to uric acid (35–65%) and the thiols of plasma proteins (10–50%), with minor roles for ascorbic acid and vitamins. An increase in TBARS and/or UA concentrations post-exercise has been found in other studies [11, 12, 25], but in agreement with our observations there were no large changes in GSH. It is worth noting that a large decrease in GSH was recorded in the cases where whole blood was analyzed [25], suggesting that the use of saliva has the advantage of avoiding artifacts due to hemolysis or contamination with erythrocytes. 53 HUMAN MOVEMENT M. de Lima Sant’Anna et al., Redox balance in athlete’s saliva In our study the GSH concentration did not change (Figure 4A), as also reported by Deminice et al. [12], who tested saliva of healthy well-trained males after a 40-min session of anaerobic resistance exercise. Even prolonged aerobic exercise of moderate intensity was not able to alter GSH concentration in skeletal muscle in healthy adults [26]. Thus GSH appears to be tightly regulated, with secretion from liver to plasma designed to ensure homeostasis in blood [27]; in our study the concentration in saliva also appeared to be tightly controlled. In another study that assessed anaerobic resistance training, Margonis et al. [25] found a decrease in GSH concentration in the blood only in association with overtraining. Wiecek et al. [28] did not measure any alteration in GSH plasma concentration 3 min after the anerobic exercise, which is in line with the saliva meaurements presented here, although the authors showed a reduction after 15 min up to 24h. Since our data only includes a collection at 5 min post aerobic exercise, this time dependent effect cannot be ruled out. Further experiments need to be performed to evaluate the time dependent behavior of GSH levels in saliva. Physical exercise triggers antioxidant adaptations [1, 29] that upregulate expression of endogenous antioxidant enzymes such as eNOS, MnSOD and iNOS expression [1, 30] as well as increases the non-enzymatic antioxidants [2]. Foti and Amorati [31] showed that uric acid accounted for one-third of the increase in antioxidant capacity suggesting that our observed increment in uric acid content in saliva represented an increase in total antioxidant capacity. Electron spin resonance and chemical studies indicate that uric acid can react with peroxyl radical, providing scavenging abilities [31]. This chemical feature may mean that uric acid helps to control oxidative stress generated by exercise, at the same time reflecting greater ATP flux associated with elevated energy requirements. Purine catabolism increases and the higher concentrations of sub-products of this metabolism are formed [32]. Xanthine oxidoreductase is a key intracellular enzyme of purine metabolism. Its oxidase form is responsible for converting hypoxanthine to xanthine and xanthine to acid uric [33]. The purine cycle generates superoxide, hydrogen peroxide, and the reactive hydroxyl molecule [34], but uric acid itself is a potent non-enzymatic antioxidant [25]. Formed in the liver from hypoxanthine, it is released to the blood and either excreted or taken up by muscle, where it scavenges hydroxyl radical [35]. Conclusions Based on the results of this study, it can be concluded that this study shows that it is possible to obtain a profile of redox state using a non-invasive approach associated with a short anaerobic test. RAST triggers free radical production, as evaluated by lipid peroxidation in saliva, and at the same time reveals an increasead antioxidant 54 capacity as a sub-acute adaptation to a short series of sprints. Acknowledgements This work was supported by grants from Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ). We wish to thank Capt. Cyro Coelho (Coach) and the Brazilian pentathlon naval’s team for their sincere cooperation. References 1. Gomez-Cabrera M.C., Domenech E., Viña J., Moderate exercise is an antioxidant: upregulation of antioxidant genes by training. Free Radic Biol Med, 2008, 44 (2), 126–131, doi: 10.1016/j.freeradbiomed.2007.02.001. 2. Powers S.K., Ji L.L., Kavazis A.N., Jackson M.J., Reactive oxygen species: impact on skeletal muscle. Compr Physiol, 2011, 1 (2), 941–969, doi: 10.1002/cphy.c100054. 3. 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Franchini E., Nunes A.V., Moraes J.M., Del Vecchio F.B., Physical fitness and anthropometrical profile of the Brazilian male judo team. J Physiol Anthropol, 2007, 26 (2), 59–67, doi: 10.2114/jpa2.26.59. 23. Chen X., Guo C., Kong J., Oxidative stress in neurodegene rative diseases. Neural Regen Res, 2012, 7 (5), 376–385, doi: 10.3969/j.issn.1673-5374.2012.05.009. 24. Wayner D.D., Burton G.W., Ingold K.U., Barclay L.R., Locke S.J., The relative contributions of vitamin E, urate, ascorbate and proteins to the total peroxyl radical-trapping antioxidant activity of human blood plasma. Biochim Biophys Acta, 1987, 924 (3), 408–419, doi:10.1016/03044165(87)90155-3. 25. Margonis K., Fatouros I.G., Jamurtas A.Z., Nikolaidis M.G., Douroudos I., Chatzinikolau A. et al., Oxidative stress biomarkers responses to physical overtraining: implications for diagnosis. Free Radic Biol Med, 2007, 43 (6), 901–910, doi: 10.1016/j.freeradbiomed.2007.05.022. 26. Quadrilatero J., Bombardier E., Norris S.M., Talanian J.L., Palmer M.S., Logan H.M. et al., Prolonged moderateintensity aerobic exercise does not alter apoptotic signaling and DNA fragmentation in human skeletal muscle. Am J Physiol Endocrinol Metab, 2010, 298 (3), E534– E547, doi: 10.1152/ajpendo.00678.2009. 27. Steinbacher P., Eckl P., Impact of oxidative stress on exercising skeletal muscle. Biomolecules, 2015, 5 (2), 356–377, doi: 10.3390/biom5020356. 28. Wiecek M., Maciejczyk M., Szymura J., Szygula Z., Kantorowicz M., Changes in non-enzymatic antioxidants in the blood following anaerobic exercise in men and women. PLoS One, 2015, 10 (11), e0143499, doi: 10.1371/journal.pone.0143499. 29. Powers S.K., Duarte J., Kavazis A.N., Talbert E.E., Reactive oxygen species are signalling molecules for skeletal muscle adaptation. Exp Physiol, 2010, 95 (1), 1–9, doi: 10.1113/expphysiol.2009.050526. 30. Ji L.L., Gomez-Cabrera M.C., Vina J., Role of nuclear factor kappaB and mitogen-activated protein kinase signaling in exercise-induced antioxidant enzyme adaptation. Appl Physiol Nutr Metab, 2007, 32 (5), 930–935, doi: 10.1139/H07-098. 31. Foti M.C., Amorati R., Non-phenolic radical-trapping antioxidants. J Pharm Pharmacol, 2009, 61 (11), 1435–1448, doi: 10.1211/jpp/61.11.0002. 32. Gerber T., Borg M.L., Hayes A., Stathis C.G., High-intensity intermittent cycling increases purine loss compared with workload-matched continuous moderate intensity cycling. Eur J Appl Physiol, 2014, 114 (7), 1513–1520, doi: 10.1007/s00421-014-2878-x. 33. Whidden M.A., McClung J.M., Falk D.J., Hudson M.B., Smuder A.J., Nelson W.B. et al., Xanthine oxidase contributes to mechanical ventilation-induced diaphragmatic oxidative stress and contractile dysfunction. J Appl Physiol (1985), 2009, 106 (2), 385–394, doi: 10.1152/japplphysiol.91106.2008. 34. Cantu-Medellin N., Kelley E.E., Xanthine oxidoreductasecatalyzed reactive species generation: a process in critical need of reevaluation. Redox Biol, 2013, 1, 353–358, doi: 10.1016/j.redox.2013.05.002. 35. Morales-Alamo D., Calbet J.A., Free radicals and sprint exercise in humans. Free Radic Res, 2014, 48 (1), 30–42, doi: 10.3109/10715762.2013.825043. Paper received by the Editor: October 26, 2015 Paper accepted for publication: February 8, 2016 Correspondence address Veronica Pinto Salerno Laboratório de Bioquímica do Exercício e Motores Moleculares (LaBEMMol) Avenida Carlos Chagas Filho, 549 Cidade Universitária CEP 21941-599, Rio de Janeiro, Brazil e-mail: vpsalerno@yahoo.com.br 55 HUMAN MOVEMENT PUBLISHING GUIDELINES – Regulamin publikowania prac 1. Human Movement (abb.: HM) is a peer-reviewed quarterly journal published by the University School of Physical Education (abb.: AWF). 2. The Editorial Office accepts for publication original empirical papers and review ones on various aspects of human movement, e.g. sports medicine, exercise physiology, biomechanics, motor control, psychology. Letters to the Editor, reports from scientific meetings and book reviews are also welcome. Publication of articles in Human Movement is free of charge. 3. Papers are accepted for publication after being reviewed favorably by at least two independent reviewers nominated by the Editor and who are not affiliated in the same research unit as the author of the reviewed manuscript. Authors can suggest reviewers, but the Editor reserves the right to final selection. 4. Review procedures are set forth in accordance with the guidelines of the Polish Ministry of Science and Higher Education which are consultable on website: https://pbn.nauka.gov.pl/ static/doc/wytyczne_dotyczace_procedury_recenzowania.pdf 5. 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Kwartalnik Human Movement (dalej: HM) jest recenzowanym czasopismem naukowym Akademii Wychowania Fizycznego we Wrocławiu (dalej: AWF). 2. Redakcja przyjmuje do publikacji oryginalne prace empiryczne oraz przeglądowe dotyczące ruchu człowieka z zakresu medycyny sportu, fizjologii wysiłku fizycznego, biomechaniki, antropomotoryki, psychologii. Przyjmowane są również listy do Redakcji, sprawozdania z konferencji naukowych i recenzje książek. Publikowanie prac w Human Movement jest bezpłatne. 3. Do druku zatwierdzane są tylko prace, które uzyskają pozytywną opinię co najmniej dwóch, powołanych przez Redakcję, niezależnych recenzentów spoza jednostki naukowej afiliowanej przez autora publikacji. Autor może zaproponować recenzentów, lecz Redakcja zastrzega sobie prawo ich doboru. 4. Procedury recenzowania są zgodne z wytycznymi Ministerstwa Nauki i Szkolnictwa Wyższego, umieszczonymi na stronie: https://pbn.nauka.gov.pl/static/doc/wytyczne_dotyczace_procedury_recenzowania.pdf 5. 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Detailed guidelines for submitting articles to Human Movement Szczegółowe zasady przygotowania artykułu do Human Movement 1. The article should be written in English. 2.Empirical research articles, together with their summary and any tables, figures or graphs, should not exceed 20 pages in length; comparative articles are limited to 30 pages. Page format is A4 (about 1800 characters with spaces per page). Pages should be numbered. 3. Articles should be written using Microsoft Word with the following formats: – Font: Times New Roman, 12 point – Line spacing: 1.5 – Text alignment: Justified – Title: Bold typeface, centered 1. Redakcja przyjmuje prace wyłącznie w języku angielskim. 2. Tekst prac empirycznych wraz ze streszczeniem, rycinami i tabelami nie powinien przekraczać 20, a prac przeglądowych – 30 stron znormalizowanych formatu A4 (ok. 1800 znaków ze spacjami na stronie). Strony powinny być ponumerowane. 3.Artykuł należy przygotować w edytorze tekstu Microsoft Word według następujących zasad: – krój pisma: Times New Roman, 12 pkt; – interlinia: 1,5; – tekst wyjustowany; – tytuł zapisany pogrubionym krojem pisma, wyśrodkowany. 57 HUMAN MOVEMENT Publishing guidelines – Regulamin publikowania prac 4. The main title page should contain the following: – The article’s title – A shortened title of the article (up to 40 characters in length including spaces), which will be placed in the running head – The name and surname of the author(s) with their affiliations written in the following way: the name of the university, city name, country name. For example: The University of Physical Education, Wrocław, Poland – Address for correspondence (author’s name, address, e-mail address and phone number) 5. The second page should contain: – The title of the article –An abstract of approximately 200 words divided into the following sections: Purpose, Methods, Results, Con clusions – Three to six keywords to be used as MeSH descriptors (terms) 6. The third page should contain: – The title of the article – The main text 7. The main body of text in empirical research articles should be divided into the following sections: 4.Strona tytułowa powinna zawierać: – tytuł pracy w języku angielskim; – skrócony tytuł artykułu w języku angielskim (do 40 znaków ze spacjami), który zostanie umieszczony w żywej paginie; – imię i nazwisko autora (autorów) z afiliacją zapisaną według następującego schematu: • nazwa uczelni, nazwa miejscowości, nazwa kraju, np. Akademia Wychowania Fizycznego, Wrocław, Polska; – adres do korespondencji (imię i nazwisko autora, jego adres, e-mail oraz numer telefonu). 5. Następna strona powinna zawierać: – tytuł artykułu; – streszczenie w języku angielskim (około 200 wyrazów) składające się z następujących części: Purpose, Methods, Results, Conclusions; – słowa kluczowe w języku angielskim (3–6) – ze słownika i w stylu MeSH. 6. Trzecia strona powinna zawierać: – tytuł artykułu; – tekst główny. 7. Tekst główny pracy empirycznej należy podzielić na następujące części: Introduction The introduction prefaces the reader on the article’s subject, describes its purpose, states a hypothesis, and mentions any existing research (literature review) Wstęp We wstępie należy wprowadzić czytelnika w tematykę artykułu, opisać cel pracy oraz podać hipotezy, stan badań (przegląd literatury). Material and methods This section is to clearly describe the research material (if human subjects took part in the experiment, include their number, age, gender and other necessary information), discuss the conditions, time and methods of the research as well identifying any equipment used (providing the manufacturer’s name and address). Measurements and procedures need to be provided in sufficient detail in order to allow for their reproducibility. If a method is being used for the first time, it needs to be described in detail to show its validity and reliability (reproducibility). If modifying existing methods, describe what was changed as well as justify the need for the modifications. All experiments using human subjects must obtain the approval of an appropriate ethnical committee by the author in any undertaken research (the manuscript must include a copy of the approval document). Statistical methods should be described in such a way that they can be easily determined if they are correct. Authors of comparative research articles should also include their methods for finding materials, selection methods, etc. Materiał i metody W tej części należy dokładnie przedstawić materiał badawczy (jeśli w eksperymencie biorą udział ludzie, należy podać ich liczbę, wiek, płeć oraz inne charakterystyczne cechy), omówić warunki, czas i metody prowadzenia badań oraz opisać wykorzystaną aparaturę (z podaniem nazwy wytwórni i jej adresu). Sposób wykonywania pomiarów musi być przedstawiony na tyle dokładnie, aby inne osoby mogły je powtórzyć. Jeżeli metoda jest zastosowana pierwszy raz, należy ją opisać szczególnie precyzyjnie, przedstawiając jej trafność i rzetelność (powtarzalność). Modyfikując uznane już metody, trzeba omówić, na czym polegają zmiany, oraz uzasadnić konieczność ich wprowadzenia. Gdy w eksperymencie biorą udział ludzie, konieczne jest uzyskanie zgody komisji etycznej na wykorzystanie w nim zaproponowanych przez autora metod (do maszynopisu należy dołączyć kopię odpowiedniego dokumentu). Metody statystyczne powinny być tak opisane, aby można było bez problemu stwierdzić, czy są one poprawne. Autor pracy przeglądowej powinien również podać metody poszukiwania materiałów, metody selekcji itp. Results The results should be presented both logically and consistently, as well as be closely tied with the data found in tables and figures. Discussion Here the author should create a discussion of the obtained results, referring to the results found in other literature (besides those mentioned in the introduction), as well as emphasizing new and important aspects of their work. 58 Wyniki Przedstawienie wyników powinno być logiczne i spójne oraz ściśle powiązane z danymi zamieszczonymi w tabelach i na rycinach. Dyskusja W tym punkcie, stanowiącym omówienie wyników, autor powinien odnieść uzyskane wyniki do danych z literatury (innych niż omówione we wstępie), podkreślając nowe i znaczące aspekty swojej pracy. HUMAN MOVEMENT Publishing guidelines – Regulamin publikowania prac Conclusions In presenting any conclusions, it is important to remember the original purpose of the research and the stated hypotheses, and avoid any vague statements or those not based on the results of their research. If new hypotheses are put forward, they must be clearly stated. Wnioski Przedstawiając wnioski, należy pamiętać o celu pracy oraz postawionych hipotezach, a także unikać stwierdzeń ogólnikowych i niepopartych wynikami własnych badań. Stawiając nowe hipotezy, trzeba to wyraźnie zaznaczyć. Acknowledgements The author may mention any people or institutions that helped the author in preparing the manuscript, or that provided support through financial or technical means. Podziękowania Należy wymienić osoby lub instytucje, które pomogły autorowi w przygotowaniu pracy, udzieliły konsultacji bądź wsparły go finansowo lub technicznie. Bibliography The bibliography should be composed of the article’s citations and be arranged and numbered in the order in which they appear in the text, not alphabetically. Referenced sources from literature should indicate the page number and enclose it in square brackets, e.g., Bouchard et al. [23]. The total number of bibliographic references (those found only in research databases such as SPORTDiscus, Medline) should not exceed 30 for empirical research papers (citing a maximum of two books); there is no limit for comparative research papers. There are no restrictions in referencing unpublished work. Bibliografia Bibliografię należy uporządkować i ponumerować według kolejności cytowania publikacji w tekście, a nie alfabetycznie. Odwołania do piśmiennictwa należy oznaczać w tekście numerem i ująć go w nawias kwadratowy, np. Bouchard et al. [23]. Bibliografia (powołania zawarte tylko w bazach danych, np. SPORTDiscus, Medline) powinna się składać najwyżej z 30 pozycji (dopuszcza się powołanie na 2 publikacje książkowe), z wyjątkiem prac przeglądowych. Niewskazane jest cytowanie prac nieopublikowanych. Citing journal articles Bibliographic citations of journal articles should include: the author’s (or authors’) surname, first name initial, article title, abbreviated journal title, year, volume or number, page number, doi, for example: Opis bibliograficzny artykułu z czasopisma Opis bibliograficzny artykułu powinien zawierać: nazwisko autora (autorów), inicjał imienia, tytuł artykułu, tytuł czasopisma w przyjętym skrócie, rok wydania, tom lub numer, strony, numer doi, np. Tchórzewski D., Jaworski J., Bujas P., Influence of long-lasting balancing on unstable surface on changes in balance. Hum Mov, 2010, 11 (2), 144–152, doi: 10.2478/v10038-010- 0022-2. Tchórzewski D., Jaworski J., Bujas P., Influence of long-lasting balancing on unstable surface on changes in balance. Hum Mov, 2010, 11 (2), 144–152, doi: 10.2478/v10038-010-0022-2. If there are six or less authors, all the names should be mentioned; if there are seven or more, give the first six and then use the abbreviation “et al.” If the title of the article is in a language other than English, the author should translate the title into English, and then in square brackets indicate the original language; the journal title should be left in its native name, for example: Gdy autorami artykułu jest sześć lub mniej osób, należy wymienić wszystkie nazwiska, jeżeli jest ich siedem i więcej, należy podać sześć pierwszych, a następnie zastosować skrót „et al.”; Tytuł artykułu w języku innym niż angielski autor powinien przetłumaczyć na język angielski, a w nawiasie kwadratowym podać język oryginału, tytuł czasopisma należy zostawić w oryginalnym brzmieniu, np. Jaskólska A., Bogucka M., Świstak R., Jaskólski A., Mechanisms, symptoms and after-effects of delayed muscle soreness (DOMS) [in Polish]. Med Sport, 2002, 4, 189–201. Jaskólska A., Bogucka M., Świstak R., Jaskólski A., Mechanisms, symptoms and after-effects of delayed muscle soreness (DOMS) [in Polish]. Med Sportiva, 2002, 4, 189–201. The author’s research should only take into consideration articles published in English. W pracy powinny być uwzględnianie tylko artykuły publikowane ze streszczeniem angielskim. Citing books Bibliographic citations of books should include: the author (or authors’) or editor’s (or editors’) surname, first name initial, book title translated into English, publisher, place and year of publication, for example: Opis bibliograficzny książki Opis bibliograficzny książki powinien zawierać: nazwisko autora (autorów) lub redaktora (redaktorów), inicjał imienia, tytuł pracy przetłumaczony na język angielski, wydawcę, miejsce i rok wydania, np. Osiński W., Anthropomotoric [in Polish]. AWF, Poznań 2001. Osiński W., Anthropomotoric [in Polish]. AWF, Poznań 2001. Heinemann K. (ed.), Sport clubs in various European countries. Karl Hofmann, Schorndorf 1999. Heinemann K. (ed.), Sport clubs in various European countries. Karl Hofmann, Schorndorf 1999. Bibliographic citations of an article within a book should include: the author’s (or authors’) surname, first name initial, article title, book author (or authors’) or editor’s (or editors’) surname, first name initial, book title, publisher, place and year of publication, paga number, for example: Opis bibliograficzny rozdziału w książce powinien zawierać: nazwisko autora (autorów), inicjał imienia, tytuł rozdziału, nazwisko autora (autorów) lub redaktora (redaktorów), tytuł pracy, wydawcę, miejsce i rok wydania, strony, np. McKirnan M.D., Froelicher V.F., General principles of exercise testing. In: Skinner J.S. (ed.), Exercise testing and exercise prescription for special cases. Lea & Febiger, Philadelphia 1993, 3–28. McKirnan M.D., Froelicher V.F., General principles of exercise testing. In: Skinner J.S. (ed.), Exercise testing and exercise prescription for special cases. Lea & Febiger, Philadelphia 1993, 3–28. 59 HUMAN MOVEMENT Publishing guidelines – Regulamin publikowania prac Citing conference materials Citing conference materials (found only in international research databases such as SPORTDiscus) should include: the author’s (or authors’) surname, first name initial, article title, conference author’s (or authors’) or editor’s (or editor’s) surname, first name initial, conference title, publisher, place and year of publication, page number, for example: Opis bibliograficzny materiałów zjazdowych Opis bibliograficzny materiałów zjazdowych (umieszczanych tylko w międzynarodowych bazach danych, np. SPORTDiscus) powinien zawierać: nazwisko autora (autorów), inicjał imienia, tytuł, nazwisko autora (autorów) lub redaktora (redaktorów), tytuł pracy, wydawcę, miejsce i rok wydania, strony, np. Rodriguez F.A., Moreno D., Keskinen K.L., Validity of a twodistance simplified testing method for determining critical swimming velocity. In: Chatard J.C. (ed.), Biomechanics and Medicine in Swimming IX, Proceedings of the IXth World Symposium on Biomechanics and Medicine in Swimming. Université de St. Etienne, St. Etienne 2003, 385–390. Rodriguez F.A., Moreno D., Keskinen K.L., Validity of a twodistance simplified testing method for determining critical swimming velocity. In: Chatard J.C. (ed.), Biomechanics and Medicine in Swimming IX, Proceedings of the IXth World Symposium on Biomechanics and Medicine in Swimming. Université de St. Etienne, St. Etienne 2003, 385–390. Citing articles in electronic format Citing articles in electronic format should include: author’s (or authors’) surname, first name initial, article title, abbreviated journal title, year of publication, journal volume and number, website address where it is available, doi number, for example: Opis bibliograficzny artykułu w formie elektronicznej Opis bibliograficzny artykułu w formie elektronicznej powinien zawierać: nazwisko autora (autorów), inicjał imienia, tytuł artykułu, tytuł czasopisma w przyjętym skrócie, tom lub numer, rok wydania, adres strony, na której jest dostępny, numer doi, np. Donsmark M., Langfort J., Ploug T., Holm C., Enevoldsen L.H., Stallknech B. et al., Hormone-sensitive lipase (HSL) expression and regulation by epinephrine and exercise in skeletal muscle. Eur J Sport Sci, 2002, 2 (6). Available from: URL: http://www.humankinetics.com/ejss/bissues. cfm/, doi: 10.1080/17461391.2002.10142575. Donsmark M., Langfort J., Ploug T., Holm C., Enevoldsen L.H., Stallknech B. et al., Hormone-sensitive lipase (HSL) expression and regulation by epinephrine and exercise in skeletal muscle. Eur J Sport Sci, 2 (6), 2002. Available from: URL: http://www.humankinetics.com/ejss/bissues. cfm/, doi: 10.1080/17461391.2002.10142575. 8. The main text of any other articles submitted for consideration should maintain a logical continuity and that the titles assigned to any sections must reflect the issues discussed within. 9. Footnotes/Endnotes (explanatory or supplementary to the text). Footnotes should be numbered consecutively throughout the work and placed at the end of the main text. 10. Tables, figures and photographs – Must be numbered consecutively in the order in which they appear in the text and provide captions –Should be placed within the text – Additionally, figures or photographs must be attached as separate files in .jpg or .pdf format (minimum resolution of 300 dpi) – May not include the same information/data in tables and also figures – Illustrative materials should be prepared in black and white or in shades of gray (Human Movement is published in such a fashion and cannot accept color) –Symbols such as arrows, stars, or abbreviations used in tables or figures should be clearly defined using a legend. 8. Tekst główny w pracach innego typu powinien zachować logiczną ciągłość, a tytuły poszczególnych części muszą odzwierciedlać omawiane w nich zagadnienia. 9.Przypisy (objaśniające lub uzupełniające tekst) – powinny być numerowane z zachowaniem ciągłości w całej pracy i umieszczone na końcu tekstu głównego. 10. Tabele, ryciny i fotografie – należy opatrzyć numerami i podpisami; – należy umieścić w tekście artykułu; – dodatkowo ryciny i fotografie trzeba dołączyć w postaci osobnych plików zapisanych w formacie *.jpg lub *.pdf (gęstość co najmniej 300 dpi); – nie można powtarzać tych samych wyników w tabelach i na rycinach; – materiał ilustracyjny powinien zostać przygotowany w wersji czarno-białej lub w odcieniach szarości (w taki sposób jest drukowane czasopismo Human Movement); – symbole, np. strzałki, gwiazdki, lub skróty użyte w tabelach czy na rycinach należy dokładnie objaśnić, tak by były czytelne i zrozumiałe niezależnie od tekstu pracy. Prior to printing, the author will receive their article in .pdf format. It is the author’s responsibility to immediately inform the Editorial Office if they accept the article for publication. At such a point in time, only minor corrections can be accepted from the author. Przed drukiem autor otrzyma swój artykuł do akceptacji w formie pliku pdf. Obowiązkiem autora jest niezwłoczne przesłanie do Redakcji Human Movement informacji o akceptacji artykułu do druku. Na tym etapie będą przyjmowane tylko drobne poprawki autorskie. SUBSCRIBING to THE HUMAN MOVEMENT JOURNAL ZASADY PRENUMERATY CZASOPISMA HUMAN MOVEMENT http://www.awf.wroc.pl/pl/article/1003/5954/Prenumerata_subscription/ 60