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Clinical Trials in Turkey / NCT07769203
Starting soon Not applicable

Effects of MET and MFR on Piriformis Syndrome

NCT07769203 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-08-30
Last updated
2026-08-17

Condition(s) studied

Piriformis Syndrome

Investigational drug(s) / intervention(s)

Muscle Energy TechniqueMyofascial Release TechniqueConventional Physical Therapy

Muscle Energy Technique: Muscle Energy Technique (MET) will be applied to participants by a trained physiotherapist in addition to conventional physical therapy. The intervention will be performed for 8 weeks, 2 sessions per week, totaling 16 sessions. The technique will include voluntary muscle contractions followed by relaxation and stretching procedures targeting the piriformis muscle.

Myofascial Release Technique: Myofascial Release Technique (MFR) will be applied to participants by a trained physiotherapist in addition to conventional physical therapy. The intervention will be performed for 8 weeks, 2 sessions per week, totaling 16 sessions. The technique will involve sustained manual pressure and soft tissue release techniques targeting the piriformis muscle and surrounding fascia.

Conventional Physical Therapy: Participants in the control group will receive conventional physical therapy for 8 weeks, 2 sessions per week, totaling 16 sessions.

Study summary

The aim of this study is to comparatively evaluate the effects of two different manual therapy approaches, Muscle Energy Technique (MET) and Myofascial Release Technique (MFR), on pain threshold, muscle activation patterns, and muscle strength in individuals diagnosed with piriformis syndrome.

In this study, the physiological effects of both interventions on the musculoskeletal system will be assessed using objective measurement tools such as an algometer, digital dynamometer, and electromyography (EMG). The study aims to provide evidence-based data regarding the most effective and preferable manual therapy approach in the conservative treatment of piriformis syndrome.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Individuals diagnosed with piriformis syndrome * Presence of piriformis tenderness and sciatic symptoms * Aged between 18 and 65 years * Voluntary agreement to participate in the study * No history of lumbar, hip, knee, or ankle surgery within the last year * Ability to cooperate with the assessment and treatment procedures Exclusion Criteria: * Individuals younger than 18 years or older than 65 years * Presence of any musculoskeletal disorder affecting the lower extremity * Presence of neurological, cardiac, pulmonary, or orthopedic disorders preventing participation in exercise * Presence of neurological deficits (muscle strength loss) * History of radiotherapy to the lumbar or hip region * Absence from more than 20% of treatment sessions * Inability to comply with the study procedures (e.g., cognitive impairment, communication problems, severe psychiatric disorders) * Corticosteroid or PRP injection within the last 3 months * Participation in another physical therapy program within the last 3 months * Use of analgesic, anti-inflammatory, or muscle relaxant medications within the last 48-72 hours * Use of psychotropic medications that may affect muscle activation or nervous system responses (e.g., antidepressants, antipsychotics, sedatives)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Hasan Kalyoncu University Faculty of Health Sciences Gaziantep Şehitkamil

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07769203 on ClinicalTrials.gov ↗ ← All trials in Turkey