- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07547059
Comparative Effects of Post Facilitation Stretch and Active Release Technique in Female Patients With Piriformis Syndrome.
Comparative Effects of Post Facilitation Stretch and Active Release Technique on Pain, Disability, Quality of Life and Range of Motion in Female Patients With Piriformis Syndrome.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Background: Piriformis syndrome (PS) is a neuromuscular condition in which the piriformis muscle irritates the sciatic nerve, causing pain, numbness, and tingling in the buttock, hip, and posterior thigh, sometimes radiating to the low back or sacroiliac joint. Women are more commonly affected, comprising 35-79% of cases (Hopayian et al., 2010). Conservative physiotherapy interventions are effective in improving pain, function, and quality of life.
Literature / Rationale: Post-Facilitation Stretch (PFS) involves isometric contraction followed by stretching of the piriformis to enhance hip range of motion (ROM) and reduce pain. Active Release Technique (ART) targets soft tissue adhesions to improve mobility and function. Prior studies indicate benefits of these techniques individually, but direct comparisons in female patients are limited.
Methods: Forty female patients with PS at NIRM Islamabad were randomly allocated via chit-box into PFS and ART groups. Interventions were administered twice weekly for 3 weeks.
PFS: Supine, hip >60° flexion, slight adduction/external rotation; 10-sec isometric external rotation contraction + 30-sec relaxation; stretch into internal rotation/adduction 15 sec; repeat 5× per session(Shahzad et al., 2020).
ART: Targeted soft tissue release of the piriformis muscle.
Outcomes included pain (measured by NPRS), hip IR and abduction ROM (measured by goniometer), functional disability (measured by LEFS-U), and quality of life (measured by SF-36), assessed at baseline, week 3, and week 6.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Islamabad, Pakistan
- Faculty of Allied Health & Biological Sciences
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 25 to 45-year-old women.
- Clinically diagnosed with piriformis syndrome by Orthopaedic Surgeon.
- Unilateral pain.
- Sitting exacerbates buttock pain.
- External soreness in the vicinity of the greater sciatic notch.
- Positive findings on standard piriformis syndrome clinical tests (FAIR, Beatty, Freiberg, and Pace).
- Limited SLR ability
Exclusion Criteria:
- History of trauma and malignancies.
- Hip dislocation, osteoporosis, and femur fractures.
- Any postural abnormality, including disc pathology.
- Patients with neurological symptom, metabolic disease (RA) and diagnosed psychological problem.
- Pregnancy.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Post Facilitation Stretch
Following a 10-minute application of a moist hot pack, participants were positioned supine with the hip flexed beyond 60° and gentle resistance was applied to facilitate an isometric external rotation contraction.
This was followed by a passive stretch held for 15 seconds, performed for 5 repetitions per session.
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Following a 10-minute application of a moist hot pack, participants were positioned supine with the hip flexed beyond 60° and gentle resistance was applied to facilitate an isometric external rotation contraction.
This was followed by a passive stretch held for 15 seconds, performed for 5 repetitions per session.
|
|
Experimental: Active Release Technique
Following a 10-minute application of a moist hot pack, participants were positioned prone, and deep manual pressure was applied over the piriformis muscle for approximately 90 seconds while the patient actively moved the hip from internal to external rotation.
This procedure was repeated for 10 repetitions per session.
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Following a 10-minute application of a moist hot pack, participants were positioned prone, and deep manual pressure was applied over the piriformis muscle for approximately 90 seconds while the patient actively moved the hip from internal to external rotation.
This procedure was repeated for 10 repetitions per session.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain Intensity
Time Frame: Assessment was done at baseline, 3rd week and 6th week
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Pain was measured by Numerical Pain Rating Scale.
On this scale, ten values range from 0 to 10, with 0 representing "no pain" and 10 representing "worst possible pain."
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Assessment was done at baseline, 3rd week and 6th week
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Disability
Time Frame: Assessment was done at baseline, 3rd week and 6th week
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Disability was measured by the Urdu version of the Lower Extremity Functional Scale.
It is a 20-item self-report questionnaire assessing functional difficulty in daily, work, and recreational activities for adults with lower limb musculoskeletal conditions.
Ranging from 0 (extreme difficulty) to 80 (high function).
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Assessment was done at baseline, 3rd week and 6th week
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Quality of life of Patients
Time Frame: Assessment was done at baseline, 3rd week and 6th week
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Quality of life was measured by the Short Form Health Survey (SF-36) questionnaire.
The overall score goes from 0 to 100.
Higher scores indicate a higher quality of life, while lower numbers indicate a lower quality of life.
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Assessment was done at baseline, 3rd week and 6th week
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Hip abduction and internal rotation range of motion
Time Frame: Assessment was done at baseline, 3rd week and 6th week
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Hip abduction and internal rotation range of motion was measured by goniometer
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Assessment was done at baseline, 3rd week and 6th week
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Collaborators and Investigators
Investigators
- Principal Investigator: Muhammad Nazim Farooq, PhD-PT, Ibadat International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IIUI/RERC/ADT/2025/04/74
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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