Myofascial Release Combined With FIFA 11+: Effects on Hamstring Flexibility and Injury Risk

March 16, 2026 updated by: Riphah International University

Effect of Myofascial Release Combined With the FIFA 11+ Program on Hamstring Flexibility and Injury Risk in Football Players

Football is a physically demanding sport that involves frequent jumping, cutting, and sudden changes in direction, making players vulnerable to various musculoskeletal injuries especially around the knee(1, 2). If not properly addressed, such mechanical demands can place excessive stress on key structures like the Hamstring, ACL and MCL, increasing the risk of injury during high-impact movement(1). Hamstring strains are one of the most common injuries among football players, with significant impact on their performance and career longevity(1). These injuries are especially prevalent due to the high-intensity nature of football, involving rapid sprinting, cutting, and changes of direction. Studies have shown that hamstring strains account for a substantial proportion of all injuries in football, ranging from 12% to 20% of total injuries in professional and amateur levels. Given the high rate of recurrence and the long recovery times associated with hamstring injuries, there has been growing interest in injury prevention programs aimed at reducing the risk of these injuries. Many of these injuries stem from deficits in dynamic balance, inadequate landing strategies, and reduced strength in the lower limbs(3). When such deficits persist, they increase biomechanical load on the knee joint, raising the likelihood of ligament injuries during explosive actions(4). By addressing these movement impairments, programs like FIFA 11+ aim to improve neuromuscular coordination and reduce injury rates among football players

Study Overview

Detailed Description

Although the FIFA 11+ program has been widely studied, there is limited evidence on its effectiveness in addressing hamstring injury-related factors combined with myofascial release among academy-level male football players in Pakistan. Most existing research focuses on professional athletes from developed countries and often lacks detailed assessments of neuromuscular and biomechanical components. Additionally, few studies have employed a randomized control design. This study will address these gaps by evaluating the FIFA 11+ program using validated assessment tools within a local youth football population.

This study will be significant, as it focuses on an underrepresented group, academy-level male football players in Pakistan, where data on injury prevention remains scarce. By examining the effects of the FIFA 11+ program on hamstring-related biomechanical and neuromuscular outcomes, the study will provide insights beyond basic injury incidence. The results will help inform effective, evidence-based warm-up strategies adapted to the local football environment.

Hamstring injuries are a frequent concern in football, often impairing player performance and longevity. A survey of male footballers from Peshawar clubs found a 53.3% prevalence of lower limb injuries, highlighting high injury risk at the grassroots level in Pakistan.

While FIFA 11+ has demonstrated strong preventive outcomes, its direct impact on flexibility is limited. Myofascial release offers an evidence-based method for improving hamstring extensibility, which could reduce strain risk. By combining MFR with FIFA 11+, this study addresses two major modifiable risk factors, flexibility deficits and poor neuromuscular control, thereby potentially reducing injuries more effectively than either approach alone.

Study Type

Interventional

Enrollment (Estimated)

28

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 Contact

Study Locations

    • KPK
      • Chakdara, KPK, Pakistan, 18800
        • Recruiting
        • Riphah international University Malakand Campus
        • Contact:
        • Principal Investigator:
          • Muhammad idrees, MS OMPT

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

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Male football players aged 16-30 years.
  • Able to comply with a 6-week FIFA 11+ program.
  • Provide informed consent.

Exclusion Criteria:

  • Acute or chronic hamstring injury.
  • Recent major surgery of the lower limb or ongoing rehab plan.
  • Inability to safely perform exercises included in the FIFA 11+ program.
  • Non-compliance with baseline assessments or the training schedule.
  • Current musculoskeletal injuries affecting lower limb function.
  • Unable to achieve ≥65% limb symmetry index (LSI) in any hop test.
  • Undergoing physiotherapy or post-rehabilitation care.

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: intervention group
The intervention group will participate in the FIFA 11+ injury prevention program, which includes a structured series of exercises designed to improve strength, balance, and neuromuscular control. The program will be conducted three times per week for Six weeks as part of their regular training schedule. Myofascial Release: Manual therapist will perform standardized MFR techniques on hamstring fascia prior to FIFA 11+ sessions, lasting 10-15 minutes.
The intervention group will participate in the FIFA 11+ injury prevention program, which includes a structured series of exercises designed to improve strength, balance, and neuromuscular control. The program will be conducted three times per week for Six weeks as part of their regular training schedule. Myofascial Release: Manual therapist will perform standardized MFR techniques on hamstring fascia prior to FIFA 11+ sessions, lasting 10-15 minutes.
Experimental: Control group

the control group will continue their standard warm-up routines without incorporating the FIFA 11+ exercises. Frequency: 3 sessions per week for 6 weeks (same as the intervention group).

Consistency: Participants will continue their usual warm-up routine without modifications.

the control group will continue their standard warm-up routines without incorporating the FIFA 11+ exercises

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Injury Surveillance Form
Time Frame: six weeks
Players' baseline information form, Injury report form, exposure report form.
six weeks
Manual Muscle Testing (MMT) for strength
Time Frame: Six weeks
to assess the muscles' strength on a scale of 5
Six weeks
Passive Straight Leg Raise (SLR) with Goniometer
Time Frame: Six weeks
to assess hamstring flexibility
Six weeks
Single-Leg Hop Test for Distance
Time Frame: Six weeks
(To assess functional outcome)
Six weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Zavata Afnan, MS NMPT, 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 15, 2025

Primary Completion (Estimated)

May 30, 2026

Study Completion (Estimated)

July 31, 2026

Study Registration Dates

First Submitted

March 16, 2026

First Submitted That Met QC Criteria

March 16, 2026

First Posted (Actual)

March 20, 2026

Study Record Updates

Last Update Posted (Actual)

March 20, 2026

Last Update Submitted That Met QC Criteria

March 16, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • REC-01025 Muhammand Idrees

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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