NCT07547059

Brief Summary

This clinical study aimed to compare the effectiveness of Post-Facilitation Stretch (PFS) and Active Release Technique (ART) on pain, disability, quality of life, and range of motion of hip internal and external rotation in female patients with piriformis syndrome. After recruitment, participants were randomly allocated into two groups using the chit-box method, either in group A Post-Facilitation Stretch, and group B Active Release Technique. Clinical outcomes including pain, disability, quality of life, and hip range of motion (abduction and internal rotation) were assessed at baseline, during the third week of treatment, and at the sixth-week follow-up from the National Institute of Rehabilitation and Medicine (NIRM) Hospital.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jun 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2025

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 15, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 15, 2025

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

April 5, 2026

Completed
18 days until next milestone

First Posted

Study publicly available on registry

April 23, 2026

Completed
Last Updated

April 23, 2026

Status Verified

April 1, 2026

Enrollment Period

7 months

First QC Date

April 5, 2026

Last Update Submit

April 20, 2026

Conditions

Keywords

Piriformis SyndromePost-Facilitation StretchActive Release TechniquePainDisabilityQuality of LifeRange of MotionFemale

Outcome Measures

Primary Outcomes (4)

  • Pain Intensity

    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."

    Assessment was done at baseline, 3rd week and 6th week

  • Disability

    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).

    Assessment was done at baseline, 3rd week and 6th week

  • Quality of life of Patients

    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.

    Assessment was done at baseline, 3rd week and 6th week

  • Hip abduction and internal rotation range of motion

    Hip abduction and internal rotation range of motion was measured by goniometer

    Assessment was done at baseline, 3rd week and 6th week

Study Arms (2)

Post Facilitation Stretch

EXPERIMENTAL

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.

Other: Post Facilitation Stretch

Active Release Technique

EXPERIMENTAL

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.

Other: Active Release Technique

Interventions

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.

Post Facilitation Stretch

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.

Active Release Technique

Eligibility Criteria

Age25 Years - 45 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsFemale
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of Allied Health & Biological Sciences

Islamabad, Pakistan

Location

MeSH Terms

Conditions

Piriformis Muscle SyndromePain

Condition Hierarchy (Ancestors)

Sciatic NeuropathyMononeuropathiesPeripheral Nervous System DiseasesNeuromuscular DiseasesNervous System DiseasesNerve Compression SyndromesNeuralgiaNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsPelvic Pain

Study Officials

  • Muhammad Nazim Farooq, PhD-PT

    Ibadat International University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 5, 2026

First Posted

April 23, 2026

Study Start

June 1, 2025

Primary Completion

December 15, 2025

Study Completion

December 15, 2025

Last Updated

April 23, 2026

Record last verified: 2026-04

Locations