Comparison of Eccentric Training on Injury Prevention and Hamstring Strength in Football Players

July 18, 2023 updated by: Riphah International University
To determine the effect of the eccentric exercise training on injury prevention and hamstring strength in football players.

Study Overview

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

Interventional

Enrollment (Actual)

36

Phase

  • Not Applicable

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

    • Balochistan
      • Quetta, Balochistan, Pakistan, 87300
        • Etihad Football Club

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

18 years to 40 years (Adult)

Accepts Healthy Volunteers

Yes

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

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

  • 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
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.
Active Comparator: control group
CONVENTIONAL EXERCISES PROGRAM GROUP The conventional exercises program will perform conventional exercises.
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.

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.
8 weeks
Anaerobic Capacity
Time Frame: 8 weeks
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.
8 weeks
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.
8 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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.
8 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Saad Rauf, Ph.D*, Riphah International University

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 (Actual)

November 1, 2022

Primary Completion (Actual)

February 1, 2023

Study Completion (Actual)

July 12, 2023

Study Registration Dates

First Submitted

January 13, 2023

First Submitted That Met QC Criteria

March 15, 2023

First Posted (Actual)

March 16, 2023

Study Record Updates

Last Update Posted (Actual)

July 19, 2023

Last Update Submitted That Met QC Criteria

July 18, 2023

Last Verified

July 1, 2023

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)?

NO

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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