- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04329273
Eccentric and Trunk Stability Exercise Program Effects in Young Soccer Players
Effects of an 8-week Eccentric and Trunk Stability Exercise Program on Muscle Strength and Postural Stability in U19 Elite Soccer Players
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
A total of 123 male Under-19 (U19) players from several soccer teams were initially invited for participation in the study after signing informed consent forms. following a second contact with the participants, questionnaire forms with inclusion and exclusion criteria were send for completion.
Based on their self-report and a clinical examination by a health professional, of the 103 players, 42 did not meet the inclusion criteria, while 12 players did not participate for personal reasons. Of the remaining 69 players, 48 players were excluded, including 3 players reporting an anterior cruciate ligament reconstruction, 14 because of lower extremity injury led to more than two weeks absence from training and 10 players because of secondary injuries or health problems that led to loss of training the past 3 months.
A neutral, blinded investigator with no further involvement in the study was responsible for randomized allocation of participants in two groups. All training sessions in the training group will be supervised by a fitness coach, who will ensure that the exercises are performed according to protocol.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Serres, Greece, 62110
- Laboratory of Neuromechanics, Department of physical education and sport sciences, Aristotle University of Thessaloniki
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- 16 to 19 years old soccer players
- Trained at least 3 times and played 1 match weekly, the past 4 years
- Healthy
- Free from muscle injuries in the 6 months prior to the study
Exclusion Criteria:
- History of anterior cruciate ligament rupture
- History of ankle, hip or knee injury with duration at least 1 week, in the 3 months prior to the study
- Muscle injury with duration at least 1 week, in the 3 months prior to the study
- Any reason resulting in 2 weeks loss of training the preceding 6 months
- Involvement in hamstring strengthening, core stability or balance training program in the 6 months prior to the study
Study Plan
How is the study designed?
Design Details
- Primary Purpose: BASIC_SCIENCE
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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EXPERIMENTAL: Training group
For the balance exercise the participants will perform one-legged stance of certain duration, on a stable surface. For the sliding leg curl exercise the participants lay supine on a mat, wearing only socks in order to create a slippery surface between their heels and the gym floor. The player begins by extending the hip and having the working leg on knee flexion. The contralateral limb is on hip flexion and knee flexion. The base of support is the shoulder blades, the elbows and the heel of the working leg. After assuming this position, the player begins to extend the knee, as slowly as possible, resisting the low friction properties of the ground. The core stability program consists of front plank, side planks, supine bridge, leg lowering and superman exercise. These exercises will be performed at the end of the training session, in contrast to the balance and hamstring exercises which will be executed before the training session. |
The exercise protocol consists of the following sets and repetitions Week 1- 2 sessions with 2 sets of 6 repetitions Week 2- 2 sessions with 3 sets of 6 repetitions Week 3- 2 sessions with 4 sets of 6 repetitions Week 4- 2 sessions with 4 sets of 8 repetitions Week 5- 2 sessions with 4 sets of 10 repetitions Week 6- 2 sessions with 4 sets of 10 repetitions Week 7- 2 sessions with 4 sets of 8 repetitions Week 8- 2 sessions with 4 sets of 8 repetitions
The exercise protocol consists of 2 sessions/week with 4 sets of 30'' single stance. Week 1 and 2- 1 set of 30'' single leg stance and 3 sets of 30'' single leg stance and ball kicks with contralateral foot Week 3 and 4- 2 sets of 30'' single leg stance while moving the ball around the leg with the contralateral foot and 2 sets of 30'' single leg stance, moving a ball around the knee with hands and kicking a ball with contralateral foot Week 5 and 6- 2 sets of 30'' single leg stance while giving and receiving hand passes with medicine ball (in couples) and 2 sets of 30'' single leg stance with perturbations (in couples) Week 7 and 8- Same as week 5 and 6 with extra 15" in each repetition
The exercise protocol consists of the following sets and repetitions Week 1 and 2- 3 sets of 30'' front plank, 3 sets of 20'' side plank, 2 sets of 30'' superman, 2 sets of 30'' supine bridge and 2 sets of 10 repetitions leg lowering exercise Week 3 and 4- increasing difficulty in 2 of the sets Week 5 and 6- adding 1 more set at each exercise Week 7 and 8- adding 15" in each repetition
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NO_INTERVENTION: Control group
The participants in this group will follow only the usual training program
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Peak concentric and eccentric torque of hamstrings and quadriceps
Time Frame: Change from baseline assessment at 8 weeks
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Peak torque (N.m) is measured using isokinetic dynamometer at each angular velocity (30°·s-1, 180°·s-1, 240°·s-1).
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Change from baseline assessment at 8 weeks
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Total sway of the center of pressure (CoP)
Time Frame: Change from baseline assessment at 8 weeks
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This is defined as the average distance (mm) of the CoP from the reference lines and the amplitude is its standard deviation
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Change from baseline assessment at 8 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Angle at peak torque of hamstrings and quadriceps
Time Frame: Change from baseline assessment at 8 weeks
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The angle at which peak torque of hamstrings and quadriceps muscles was achieved, at each angular velocity, measured in degrees (°)
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Change from baseline assessment at 8 weeks
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Conventional hamstrings to quadriceps ratio
Time Frame: Change from baseline assessment at 8 weeks
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This is calculated by dividing peak isokinetic concentric hamstring strength by the peak isokinetic concentric quadriceps strength, at the same angular velocity
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Change from baseline assessment at 8 weeks
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Dynamic hamstrings to quadriceps ratio
Time Frame: Change from baseline assessment at 8 weeks
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This is calculated by dividing peak isokinetic eccentric hamstring strength by the peak isokinetic concentric quadriceps strength, at the same angular velocity
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Change from baseline assessment at 8 weeks
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Mixed hamstrings to quadriceps ratio
Time Frame: Change from baseline assessment at 8 weeks
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This is calculated by dividing peak isokinetic eccentric hamstring strength at 30°·s-1 by the peak isokinetic concentric quadriceps strength at 240°·s-1
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Change from baseline assessment at 8 weeks
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Average speed of CoP
Time Frame: Change from baseline assessment at 8 weeks
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This reflects the amplitude and frequency of CoP movements and is calculated as the total length of the path of CoP divided by the test trial time (mm·s-1 )
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Change from baseline assessment at 8 weeks
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Konstantinos Dafkou, Laboratory of Neuromechanics, Aristotle University of Thessaloniki
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- ERC-005/2020
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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