The Effect of Myofascial Release Technique on Sportive Performance, Balance and Injury Risk in Runners

Medipol Health Group

Status: Unknown

Conditions: Runt

Treatments: Other: Myofascial therapy

Study type: Interventional

Funder types: Other

Identifiers

NCT05392153

E-10840098-772.02-2678

Details and patient eligibility

About

In order to investigate the effect of myofascial release technique on sportive performance, balance and injury risk in runners, 49 athletes will include in the study. The myofascial application group (n=26)will receive 12 sessions of 6-weekly lower extremity posterior muscle therapy. The control group (n=23) will continue the routine exercise program.

Full description

Running is a sport that involves repetitive movement and is particularly vulnerable to injury in the lower extremities. Myofascial release, on the other hand, is a manual method that is effective in increasing blood and oxygen permeability between tissues, renewing the tissue, protecting it from injury and increasing performance. The aim of our study is to investigate the effect of Myofascial application on sportive performance balance and injury risk in runners. The study will carry out on runners with a 3-month running history. Myofascial application group (n=26) and control group (n=23) will divide into two groups as randomized controlled. My Jump 2 App, Y balance test and Functional Movement Analysis (FMS) will use as assessment methods. The myofascial application group will receive 12 sessions of 6 weeks of therapy for the lower extremity posterior group muscles. The control group will continue the routine exercise program.

Enrollment: 49 estimated patients

Sex: All

Ages: 18 to 45 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Have a running history of more than 3 months
• Be between 18 and 45 years old
• Being a healthy individual without chronic disease
• No acute injury affecting the lower extremity
• Running at least 5 km a week
• Willingness to participate in the research

Exclusion criteria

• Pregnancy or suspected pregnancy
• Use of alcohol or active substance
• Having another ongoing treatment process
• Having a history of surgery on the lower extremity
• Refusal to participate in the study

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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49 participants in 2 patient groups

Myofascial therapy group

Experimental group

Description:

The myofascial therapy group (n=26) will receive 12 sessions of 6-weekly lower extremity posterior muscle myofascial therapy.

Treatment:

Other: Myofascial therapy

Control group

No Intervention group

Description:

The control group (n=23) will not receive lower extremity posterior muscle myofascial therapy. They will continue the routine exercise program.