THE MYOFASCIAL SYSTEM AND MINIMIZING THE RISK OS INJURY IN SPORT

November 25, 2025 updated by: Bruno Ferreira Rondon Linhares, Aveiro University

EFFECT OF SELF-MYOFASCİAL RELEASE ON MUSCLE MECHANİCAL PROPERTİES, PERFORMANCE, NEUROMUSCULAR FUNCTİON AND MİNİMİZATİON OF İNJURY RİSK İN YOUNG SOCCER PLAYERS

The aim of the study is to evaluate the effect of myofascial self-release on muscle mechanical properties, performance, neuromuscular function, and injury risk reduction in young soccer players. The hypothesis is a reduction in the number of injuries in the experimental group, as well as improvements in muscle mechanical properties, performance, and neuromuscular function in young soccer players.The study will be a randomized clinical trial with a convenience sample of approximately 65 male athletes aged between 14 and 18 years, divided into control and experimental groups. Athletes with no history of injury in the three months prior to the study will be included, while those with a history of previous surgery or lower limb fractures in the past five years, or who are undergoing physiotherapy at the time of the study, will be excluded.Muscle mechanical properties (myotonometry), flexibility (sit-and-reach test), ankle dorsiflexion range of motion (Weight Bearing Lunge Test), motor control (Y Balance Test), and the reactive strength index (Myjump App) will be assessed before, immediately after, and at 8 and 16 weeks post-intervention. Myofascial self-release will be performed bilaterally on the quadriceps, hamstrings, and calves for 2 minutes per region, twice a week, using a structured massage roller. All procedures will be demonstrated beforehand during the study.

For the Myoton procedure, the athlete will simply lie in a supine and prone position on the examination table. The athlete will only be asked to remain still in the "face-up" or "face-down" position, feeling only the light contact of the device's probe, which is painless and will be demonstrated beforehand.

In the Y Balance Test, athletes will be asked to balance on one foot atop a grid placed on the floor, with their hands on their hips, and reach as far as possible with the non-supporting leg in three marked directions on the floor, without lifting the heel of the supporting leg.

For the Ankle Range of Motion - Weight Bearing Lunge Test, the athlete will place the tested foot on a measuring tape positioned on the floor and will be instructed to touch their knee to the wall in front of them without lifting the heel of the tested foot. Three attempts will be allowed, and the longest distance from the big toe to the wall will be recorded.

In the Sit-and-Reach Test, the athlete will sit on the floor with bare feet and both legs extended. They will be instructed to keep their hands side by side and try to reach the greatest possible distance on the ruler in front of them by bending forward without bending their legs, holding the position for one second to measure the distance. Three attempts will be allowed, and the greatest distance reached will be recorded.

For ground reaction strength, the athlete will be asked to jump off a 40 cm high box, and as soon as their feet touch the ground, they will be encouraged to jump upward as quickly and as high as possible.

In myofascial self-release, athletes in the experimental group will be asked to use the myofascial release roller for 2 minutes before training on each of the three muscle groups - anterior and posterior thigh and posterior leg. Athletes will be instructed to roll using as much pressure as possible on the roller. For the anterior thigh, they will roll across the entire front part of the thigh; for the posterior thigh, they will roll from just below the gluteal region to just above the knee; and for the posterior leg, they will roll from just below the knee to just above the heel.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

65

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

    • Porto District
      • Fão, Porto District, Portugal, 4740-364

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

No

Description

Inclusion Criteria:

  • Athletes at the youth and junior levels
  • Registered with the respective football association
  • Athletes with no history of injury in the past 3 months

Exclusion Criteria:

  • Athletes who failed pre-season medical examinations
  • Athletes with a history of previous surgery or lower limb fractures in the last 5 years
  • Athletes undergoing physiotherapy rehabilitation at the time of the study
  • Athletes participating in another injury prevention program or specific training

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental Group - Myofascial Self-Release
In this group, the following will be evaluated: muscle mechanical properties using the Myoton, flexibility using the sit-and-reach test, dorsiflexion range of motion using the Weight Bearing Lunge Test, motor control using the Y Balance Test, and the reactive strength index using the Myjump App. Myofascial self-release will be performed using a structured roller.
Athletes will be asked to use the myofascial release roller for 2 minutes before training on each of the three muscle groups: anterior and posterior thigh and posterior leg. They will be instructed to roll while applying as much pressure as possible on the roller. For the anterior thigh, the roller will be moved along the entire front part of the thigh; for the posterior thigh, it will be rolled from just below the gluteal region to just above the knee; and for the posterior leg, it will be rolled from just below the knee to just above the heel.
Other Names:
  • Foam rolling
No Intervention: No Intervention: Control Group
Athletes will maintain regular training sessions

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Incidence of sports injuries
Time Frame: Until the completion of the studies, an average of 5 months.
Monitor the incidence of injuries in the control and experimental groups
Until the completion of the studies, an average of 5 months.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evaluate Muscle Mechanical Properties
Time Frame: For a period of 8 and 16 weeks
Muscle elasticity will be assessed using myotonometry.
For a period of 8 and 16 weeks
Evaluate Muscle Mechanical Properties
Time Frame: For a period of 8 and 16 weeks
Tone will be assessed using myotonometry.
For a period of 8 and 16 weeks
Evaluate Muscle Mechanical Properties
Time Frame: For a period of 8 and 16 weeks
Stiffness will be assessed using myotonometry.
For a period of 8 and 16 weeks
Evaluate Neuromuscular Control
Time Frame: For a period of 8 and 16 weeks
Neuromuscular control will be assessed using the Y Balance Test.
For a period of 8 and 16 weeks
Evaluate Ankle Dorsiflexion Range of Motion
Time Frame: For a period of 8 and 16 weeks
Ankle dorsiflexion range of motion will be assessed using the Weight-Bearing Test.
For a period of 8 and 16 weeks
Evaluate Flexibility
Time Frame: For a period of 8 and 16 weeks
Flexibility will be assessed using the Sit and Reach Test.
For a period of 8 and 16 weeks
Evaluate the Reactive Strength Index
Time Frame: For a period of 8 and 16 weeks
The Reactive Strength Index will be assessed using the MyJump application.
For a period of 8 and 16 weeks
Evaluate the Jump Height
Time Frame: For a period of 8 and 16 weeks
The Jump Height will be assessed using the MyJump application.
For a period of 8 and 16 weeks
Evaluate the air time after the jump
Time Frame: For a period of 8 and 16 weeks
The air time after jump will be assessed using the MyJump application.
For a period of 8 and 16 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this 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 (Estimated)

January 1, 2026

Primary Completion (Estimated)

February 26, 2026

Study Completion (Estimated)

April 30, 2026

Study Registration Dates

First Submitted

March 5, 2025

First Submitted That Met QC Criteria

March 19, 2025

First Posted (Actual)

March 26, 2025

Study Record Updates

Last Update Posted (Actual)

December 2, 2025

Last Update Submitted That Met QC Criteria

November 25, 2025

Last Verified

November 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 12-CED/2024

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.

Clinical Trials on Muscle Stiffness

Clinical Trials on Myofascial Self-Release

Subscribe