- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04456374
Performance Testing in Young Soccer Players
June 28, 2020 updated by: Ioannis G. Fatouros, University of Thessaly
Evaluation of Soccer-specific Performance and Body Composition in Youth Soccer Players of Different Age Groups
The aim of this study is to investigate physiological characteristics, body composition and performance indicators among youth soccer players of four age categories (U-12, U-14, U-16, and U-18).
Participants will undergo assessment of their body weight, body height and percent of body fat as well as performance testing including flexibility, strength, vertical jump, speed, repeated sprint ability, agility, dribbling and endurance.
Study Overview
Detailed Description
This study aims at investigating anthropometric, body composition and performance indicators among male youth soccer players.
The study will be conducted prior to the preparation period.
Initially, participants and their parents (for those under 18 years) will be informed about the benefits, risks and discomforts associated with the study and will provide a written consent.
Participants will be instructed to refrain from strenuous exercise for at least 48 hours prior to testing and they will be also asked to consume their normal diet.
Prior to testing all participants will be familiarized with testing procedures and specific test.
Body weight will be measured on a seca beam balance.
Participants' height will be measured by using a fixed stadiometer and the percent body fat will be calculated with bioelectrical impedance analysis.
Flexibility will be assessed by using the sit and reach test and the lower body explosive strength will be determined through vertical jump testing (squat jump and counter movement jump without arm swing).
Knee flexor and extensor strength will be assessed on an isokinetic dynamometer.
Sprint performance will be assessed from a standing start over by infrared photocells with participants running 10m and 30m as fast as they can.
The repeated sprint ability will be tested by using linear sprint test including 5 maximum sprints of 30 meters with a 25-second recovery period in-between.
Maximal oxygen consumption (VO2max) will be determined by open-circuit spirometry via breath-by-breath analysis during a graded exercise test to exhaustion on a treadmill.
Furthermore, participants will be evaluated in agility by using the short dribbling test and the ability to recover after repeated intense exercise through the YO-YO Intermittent Recovery test 1 (only for u-16 and U-18 groups).
Study Type
Observational
Enrollment (Anticipated)
120
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Trikala, Greece, 42100
- University of Thessaly, School of Physical Education and Sports Science
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
11 years to 18 years (ADULT, CHILD)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Sampling Method
Non-Probability Sample
Study Population
Youth soccer players (aged 11-18 years) participating in regular soccer practice and competition with a training age of ≥ 3 years.
Description
Inclusion Criteria:
- Aged between 11 and 12 years
- Active soccer players participating in regular soccer practice and competition
- Training age ≥ 3 years
- Free of chronic diseases
- Free of musculoskeletal injury
Exclusion Criteria:
- Musculoskeletal injury
- Chronic disease
- Training age ≤ 2 years
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Under-12 (U12) players
|
Soccer-specific performance will be evaluated by measuring flexibility, jumping ability, maximum speed, repeated spring ability, agility and endurance.
|
|
Under-14 (U14) players
|
Soccer-specific performance will be evaluated by measuring flexibility, jumping ability, maximum speed, repeated spring ability, agility and endurance.
|
|
Under-16 (U16) players
|
Soccer-specific performance will be evaluated by measuring flexibility, jumping ability, maximum speed, repeated spring ability, agility and endurance.
|
|
Under-18 (U18) players
|
Soccer-specific performance will be evaluated by measuring flexibility, jumping ability, maximum speed, repeated spring ability, agility and endurance.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Flexibility
Time Frame: At baseline
|
Flexibility will be assessed by using the sit-and-reach test
|
At baseline
|
|
Jumping ability
Time Frame: At baseline
|
Jumping ability will be assessed by measuring the vertical jumping performance using two different techniques: i) countermovement and ii) squat jump.
|
At baseline
|
|
Maximum speed
Time Frame: At baseline
|
Maximum speed will be assessed over 10 m and 30 m by using light cells
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At baseline
|
|
Repeated sprint ability
Time Frame: At baseline
|
Repeated sprint ability will be assessed by performing five 30-m sprints with 25 seconds recovery period in-between, and using light cells.
|
At baseline
|
|
Agility
Time Frame: At baseline
|
The ability to change direction while dribbling the ball (termed agility) will be assessed by using the short dribbling test (performed according to standard procedures).
|
At baseline
|
|
Endurance
Time Frame: At baseline
|
Endurance will be assessed by using the Yo-Yo Intermittent Recovery test level 1
|
At baseline
|
|
Maximal oxygen consumption (VO2max)
Time Frame: At baseline
|
Maximal oxygen consumption will be measured by open-circuit spirometry via breath-by-breath analysis during a graded exercise test to exhaustion on a treadmill, using automated pulmonary gas exchange system.
|
At baseline
|
|
Knee flexor and extensor strength
Time Frame: At baseline
|
Concentric and eccentric peak torque of knee flexors and extensors in both limbs (dominant and non-dominant) will be assessed on an isokinetic dynamometer
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At baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Body height
Time Frame: At baseline
|
Body height will be measured on a beam balance with stadiometer.
|
At baseline
|
|
Body weight
Time Frame: At baseline
|
Body weight will be measured on a beam balance with stadiometer.
|
At baseline
|
|
Body composition
Time Frame: At baseline
|
Body fat and fat-free mass will be estimated by using bioelectrical impedance.
|
At baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Athanasios Poulios, PhD, University of Thessaly
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ANTICIPATED)
August 5, 2020
Primary Completion (ANTICIPATED)
August 30, 2020
Study Completion (ANTICIPATED)
September 10, 2020
Study Registration Dates
First Submitted
June 24, 2020
First Submitted That Met QC Criteria
June 28, 2020
First Posted (ACTUAL)
July 2, 2020
Study Record Updates
Last Update Posted (ACTUAL)
July 2, 2020
Last Update Submitted That Met QC Criteria
June 28, 2020
Last Verified
June 1, 2020
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- YOUTH SOCCER STUDY-UTH-2020
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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