- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07484698
Myofascial Release Combined With FIFA 11+: Effects on Hamstring Flexibility and Injury Risk
Effect of Myofascial Release Combined With the FIFA 11+ Program on Hamstring Flexibility and Injury Risk in Football Players
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Zavata Afnan, MS NMPT
- Phone Number: 03434411214
- Email: Zavata.afnan@riphah.edu.pk
Study Locations
-
-
KPK
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Chakdara, KPK, Pakistan, 18800
- Recruiting
- Riphah international University Malakand Campus
-
Contact:
- Zavata Afnan, MS NMPT
- Phone Number: 03434411214
- Email: Zavata.afnan@riphah.edu.pk
-
Principal Investigator:
- Muhammad idrees, MS OMPT
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
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
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
Sponsor
Investigators
- Principal Investigator: Zavata Afnan, MS NMPT, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
- REC-01025 Muhammand Idrees
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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