- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05771792
Comparison of Eccentric Training on Injury Prevention and Hamstring Strength in Football Players
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Hamstrings injuries are common among footballers with a higher prevalence rate in male footballers. Despite the relatively high incidence of hamstring injuries in sports, no clear prevention methods have been identified. Most hamstring muscle injuries occur during an eccentric phase of any activity. Eccentric hamstring training has been used for injury prevention in recent years. The two distinguishing characteristics of eccentric muscle contractions have been well understood: 1) great force output; and 2) low energy cost to produce the force. Due to these distinguishing characteristics, eccentric exercise is widely used in injury prevention programs.
The aim of this study is to determine the effectiveness of eccentric training as compared to conventional training in hamstring muscle injury prevention and strengthing in football players.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Balochistan
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Quetta, Balochistan, Pakistan, 87300
- Etihad Football Club
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Football players with age 18 to 40
- Male
- Players playing football for > 1 year
Exclusion Criteria:
- Having history of injury and surgery in past
- Those players having any kind of musculoskeletal, neurological, cardiovascular, or degenerative problems
- Those players who have any medical conditions
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: eccentric exercise group
SPECIFIC MODIFIED EXERCISE PROGRAM GROUP The modified exercise group will perform 6 exercises
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Eccentric Exercise training group will perform 8 weeks of protocol with a total 24 sessions for 45 minutes (3 session per week).
During each 45 minutes training session, subjects will complete the warmup for 10 minutes, Eccentric Exercise training for 25 minutes and cool down 10minutes.
All players will perform each repetition in a slow, controlled manner, 10 repetition and 3 sets in first 4 week and 15 repetition and 3 sets in last 4 weeks of all exercises for 45 minutes.
Eccentric exercise training protocol is as follow: Prone Hamstring Curl, Seated TheraBand Hamstring Curl, Exercise Ball (or glider) Bridge with Curl, Stiff-Legged Deadlift, Single Leg Deadlift, Nordic Hamstring Curl.
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|
Active Comparator: control group
CONVENTIONAL EXERCISES PROGRAM GROUP The conventional exercises program will perform conventional exercises.
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The participant of the Control Group will perform 8 weeks of protocol with a total 24 sessions for 45 minutes (3 session per week).
During each 45 minutes training session, subjects will complete the warmup for 10 minutes, conventional training for 25 minutes and cool down 10minutes.
All players will perform each repetition in a slow, controlled manner, 10 repetition and 3 sets in first 4 week and 15 repetition and 3 sets in last 4 weeks of all exercises for 45 minutes.
The exercise will be as follow: Side Lunges, Split Squats, Calf Raises.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hamstring Strength
Time Frame: 8 weeks
|
Vertical jumps: The person puts chalk on their finger tips to mark the wall at the height of their jump.
The person then stands away from the wall, and jumps vertically as high as possible using both arms and legs to assist in projecting the body upwards.
Attempt to touch the wall at the highest point of the jump.
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8 weeks
|
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Anaerobic Capacity
Time Frame: 8 weeks
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SPRINT FATIGUE TEST: A repeat sprint test of anaerobic capacity consisting of ten 30-second sprints.
This is an anaerobic capacity test, which measures the ability to recover between sprints while maintaining the same level of strength.
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8 weeks
|
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Agility
Time Frame: 8 weeks
|
5-0-5 AGILITY TEST: The ability to turn 180 degrees is measured by the 505 Agility test.
The test can also be modified for sport-specific testing by having the subject dribble a soccer ball, a hockey puck, or a basketball through the course.
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8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Injury Prevention ( FASH )
Time Frame: 8 weeks
|
FASH (Functional assessment scale for acute hamstring injuries) questionnaire is a self-administered questionnaire used for acute hamstring injuries assessment.
It is a valid and reliable instrument for assessing and determining the severity of hamstring injuries in an athlete population.
It is a 10-item questionnaire that look the ability of a patient to perform certain lower extremity activities.
This is a self-report questionnaire that patient can rate difficulty and interference with daily life.
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8 weeks
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Saad Rauf, Ph.D*, Riphah International University
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/01404 Shivam Sachdev
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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