- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07474597
Investigation of the Effectiveness of Myofascial Release Techniques Applied to the Popliteus Muscle in Individuals With Knee Pain.
March 15, 2026 updated by: Aysegul Kutsal, Istanbul Rumeli University
This study aimed to evaluate the effectiveness of popliteus muscle-targeted myofascial release techniques (MFR) when added to conventional physical therapy and rehabilitation (PTR) and exercise protocols in patients with knee pain.
Study Overview
Detailed Description
This study aimed to evaluate the effectiveness of popliteus muscle-targeted myofascial release techniques (MFR) when added to conventional physical therapy and rehabilitation (PTR) and exercise protocols in patients with knee pain.
Sixty patients presenting with knee pain were assessed according to inclusion and exclusion criteria, and 45 eligible participants were enrolled.
Participants were allocated into two groups: the popliteus group (23) and the control group (22).
Assessments were performed before treatment and after treatment.
Both groups received a standard PTR program consisting of heat therapy (20 min), transcutaneous electrical nerve stimulation (TENS) (20 min), therapeutic ultrasound (US) (4 min), and exercises, administered 5 days per week for a total of 10 sessions.
In addition, popliteus muscle-targeted MFR techniques were applied to the popliteus group.
Outcome measures included pain (visual analog scale, VAS), functional status (Western Ontario and McMaster Universities Osteoarthritis Index, WOMAC), quality of life (Short Form-12 Health Survey, SF-12), range of motion (ROM), limb circumference measurement, and balance tests (single-leg stance test, SLST).
Study Type
Interventional
Enrollment (Actual)
45
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 Locations
-
-
-
Istanbul, Turkey (Türkiye)
- İstanbul Fatih Sultan Mehmet Eğitim ve Araştırma Hastahanesi
-
-
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
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Being between 18-70 years of age
- Being able to communicate in Turkish
- Being literate
- Having a diagnosis of non-specific knee pain, Patellafemoral pain syndrome, or Knee Osteoarthritis
- Volunteering to participate in the study
Exclusion Criteria:
- Having undergone surgery on the knee joint
- Having a diagnosis of inflammatory rheumatism
- Having a significant clinical infection
- Having a fracture in the bones forming the knee joint
- Having received cortisol treatment within the last 6 months
- Having a disease that prevents the patient from lying prone
- Having a history of deep vein thrombosis
- Having severe varicose vein disease
- Being an active cancer patient
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: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Popliteus
Myofascial Release Techniques Applied to the Popliteus Muscle
|
Classical Myofascial Release
|
|
No Intervention: Kontrol Grubu
Myofascial Release uygulanmadı
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Myofascial Release Techniques AppliMeasurement of quality of life in individuals with knee pain following myofascial release techniques applied to the popliteus muscle.
Time Frame: 5 days 10 sessions
|
Measurement of quality of life in individuals with knee pain following myofascial release techniques applied to the popliteus muscle.
The SF-12 scale was used as the measurement.
Patella circumference measurements were also taken.
|
5 days 10 sessions
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Ali CIMBIZ, Istanbul Rumeli Universitesi
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)
October 1, 2025
Primary Completion (Actual)
January 2, 2026
Study Completion (Actual)
January 2, 2026
Study Registration Dates
First Submitted
January 29, 2026
First Submitted That Met QC Criteria
March 11, 2026
First Posted (Actual)
March 16, 2026
Study Record Updates
Last Update Posted (Actual)
March 17, 2026
Last Update Submitted That Met QC Criteria
March 15, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRU-FTR-AK-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Sharing Supporting Information Type
- SAP
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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