Myofascial Release Techniques in Football Players

June 11, 2025 updated by: Musa Güneş, Karabuk University

Investigation of Acute Effects of Myofascial Release Techniques on Jumping Performance, Balance, and Proprioception in Football Players

Fascial tissue ensures optimal function and mobility by providing gliding and force transfer during movement. However, fascial order can be disrupted in cases such as overuse and trauma. Therefore, treatment of fascial tissue is important. Therefore, this study aimed to investigate the effects of different myofascial release techniques on jumping performance, flexibility, balance, and proprioception in amateur football players.

Study Overview

Detailed Description

Fascial tissue ensures optimal function by providing gliding and force transfer during movement. It is also associated with an increase in functional capacity by providing flexibility. However, excessive exercise, incorrect movements, and excessive load on the tissue cause dysfunctions in the fascial tissue, leading to myofascial limitations. Elimination of these limitations is important for the maintenance of optimal function. Fascia also provides sensory transmission as a proprioceptive organ. Myofascial limitations also cause problems in sensory organization, leading to injuries and injuries. For this reason, a decrease in flexibility, balance, and sports functions can be observed. Various methods are used to eliminate this myofascial limitation, and there is an increasing demand for myofascial release techniques in many areas daily. The effects of different myofascial release techniques have been examined in the literature in various disease groups and sports injuries, and their effects on joint range of motion, pain, and flexibility have been shown. However, since there are different release techniques, information on which method is more effective or the optimal usage period is unclear. Therefore, this study aimed to investigate the effects of different myofascial release techniques applied with Graston and foam roller on jumping performance, flexibility, balance, and proprioception in amateur football players.

Study Type

Interventional

Enrollment (Estimated)

48

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

      • Karabük, Turkey
        • Recruiting
        • Karabuk University, Physiotherapy and Rehabilitation Application and Research Center
        • Contact:

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Being between the ages of 18-35
  • Being able to communicate in Turkish
  • Being willing to participate in the study.
  • Being a licensed football player

Exclusion Criteria:

  • Those with a body mass index of 30 kg/m² or higher
  • Those with a history of lower extremity surgery in the last 6 months
  • Those with cardiac, musculoskeletal, vestibular, and neurological problems
  • Those with mental, perceptual problems (Mini-mental test score <24)

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: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control
No intervention will be applied to the control group.
Experimental: Fascial release with instrument assisted soft tissue mobilization
The fascial release group will be treated with the Graston device to the superficial and deep fascia of the hamstrings and the gastro-soleus muscle complex.
The fascial release group will be treated with the Graston device to the superficial and deep fascia of the hamstrings and the gastro-soleus muscle complex in both extremities for a total of 16 minutes.
Experimental: Fascial release with foam roller
The fascial release group will be treated with the self-foam roller treatment to the fascia of the hamstrings and the gastro-soleus muscle complex.
Fascial release with a foam roller will be applied to the fascia of the hamstring and gastro-soleus muscle complex with a self-foam roller for a total of 16 minutes.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Jumping perfomance
Time Frame: baseline, immediately after the intervention
My Jump 2, a mobile app designed for vertical jump performance, high-speed video capture
baseline, immediately after the intervention
Proprioception
Time Frame: baseline, immediately after the intervention
Proprioception will be evaluated with an inclinometer at a 30-45 degree angle.
baseline, immediately after the intervention
Balance
Time Frame: baseline, immediately after the intervention
The Y Balance Test (YBT) will ve used for evaluating dynamic balance across three reach directions: anterior (ANT), posteromedial (PM), and posterolateral (PL)
baseline, immediately after the intervention
Flexibilty
Time Frame: baseline, immediately after the intervention
Flexibility will be assessed with a sit-and-reach test.
baseline, immediately after the intervention

Collaborators and Investigators

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

Investigators

  • Study Director: Musa Güneş, PhD, Karabuk University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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)

April 28, 2025

Primary Completion (Estimated)

September 30, 2025

Study Completion (Estimated)

December 31, 2025

Study Registration Dates

First Submitted

April 28, 2025

First Submitted That Met QC Criteria

April 28, 2025

First Posted (Actual)

May 6, 2025

Study Record Updates

Last Update Posted (Actual)

June 15, 2025

Last Update Submitted That Met QC Criteria

June 11, 2025

Last Verified

June 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Karabuk-2282

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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