NCT07484373

Brief Summary

The study was conducted to determine the effects of hip abductor strengthening exercises on pain, range of motion, and lower extremity function in patients with piriformis syndrome.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
48

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 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

January 13, 2025

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 31, 2025

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 31, 2025

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

March 16, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

March 20, 2026

Completed
Last Updated

March 20, 2026

Status Verified

March 1, 2026

Enrollment Period

5 months

First QC Date

March 16, 2026

Last Update Submit

March 16, 2026

Conditions

Keywords

Piriformis syndrome PainQuality of lifeHip abductor strengthening exercisesLower Extremity Functional Scale

Outcome Measures

Primary Outcomes (2)

  • Lower Extremity Functional Scale (LEFS)

    The Lower Extremity Functional Scale (LEFS) is a self-reported questionnaire used to assess lower extremity functional status in individuals with musculoskeletal conditions. It consists of 20 items related to daily activities such as walking, climbing stairs, squatting, and running. Each item is scored on a 5-point Likert scale (0 = extreme difficulty/unable to perform, 4 = no difficulty), with a maximum total score of 80. Higher scores indicate better functional ability. The LEFS is widely used due to its high reliability, validity, and responsiveness in evaluating functional improvement over time.

    From enrolment to the end of treatment at 4 weeks

  • Numeric Pain Rating Scale (NPRS)

    The Numeric Pain Rating Scale (NPRS) is a subjective measure used to assess pain intensity. Patients are asked to rate their current pain level on a scale from 0 to 10, where 0 represents "no pain" and 10 represents "worst imaginable pain." It is simple, quick to administer, and clinically reliable for monitoring changes in pain over time. A reduction of 2 points or more is generally considered clinically meaningful improvement

    from enrollment to the end of treatment at 4 weeks

Secondary Outcomes (2)

  • Hip Abduction range of motion

    from enrollment to the end of treatment.

  • Hip external roration ROM

    From enrollment to the end of treatment at 4 weeks.

Study Arms (2)

Arm 1: Hip Abductor Strengthening Exercise Group + conventional physiotherapy

EXPERIMENTAL
Other: Progressive Hip Abductor Strengthening ExercisesOther: conventional physiotherapy treatment

Arm 2: Conventional Physiotherapy Group

ACTIVE COMPARATOR
Other: conventional physiotherapy treatment

Interventions

Experimental Group (Hip Abductor Strengthening + Baseline Physiotherapy) A structured hip abductor strengthening program divided into three progressive phases over four weeks, along with baseline physiotherapy treatment. Phase I (Week 1 - Non-weight bearing / Isolated activation) Exercises: Bridging, Side-lying clam exercises, Side-lying hip abduction, Towel squeeze Dosage: 3 × 15 repetitions Phase II (Week 2 - Weight-bearing strengthening) Exercises: Squats, Side-stepping, Single-limb sit-to-stand, Step-up/Step-down, Leg press Dosage: 3 × 15 repetitions Phase III (Weeks 3-4 - Dynamic/Functional training) Exercises: Forward lunges, Double-limb jump Dosage: Week 3 → 3 × 15 repetitions Week 4 → 5 × 20 repetitions

Arm 1: Hip Abductor Strengthening Exercise Group + conventional physiotherapy

conventional Physiotherapy treatment * Hydro-collateral pack for 10 minutes over piriformis muscle (40°C) * Pulsed ultrasound for 10 minutes at 2.25 W/cm² * Piriformis stretching maneuver (20-second hold × 10 repetitions)

Arm 1: Hip Abductor Strengthening Exercise Group + conventional physiotherapyArm 2: Conventional Physiotherapy Group

Eligibility Criteria

Age18 Years - 45 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Males and Females between 18 and 45 .
  • Unilateral involvement, Onset of pain not \> 2 weeks.
  • Grade 1-3 Tenderness at piriformis muscle.
  • Numeric pain rating scale\>3and equal to, \<6.
  • Any three positive test among Piriformis Test, Beatty Test, Freiberg Test, FAIR Test, Sign of Pace \& Nagel.

You may not qualify if:

  • Positive Leagues' sign.
  • Any pathology or recent injury around hip, knee and SI joint .
  • Fracture of femur \& hip joint dislocation.
  • Pain due to neurological, spinal or pelvic origin.
  • Limb length discrepancy .
  • Stenosis of spine and disc herniation .
  • Any postural abnormality/ deformity .
  • Tumors and facet joint pathology.
  • Congenital or acquired abnormality in the spinal column .
  • Pregnancy .
  • Neurological conditions like, CVA, Parkinson's disease, non-cooperative \& subjects with psychological impairment .

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hashir Ali clinic

Lahore, Punjab Province, 40100, Pakistan

Location

MeSH Terms

Conditions

Piriformis Muscle Syndrome

Condition Hierarchy (Ancestors)

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

Study Officials

  • Humera Mubashar, Ms-OMPT

    Riphah International University

    PRINCIPAL INVESTIGATOR

Study Design

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

Study Record Dates

First Submitted

March 16, 2026

First Posted

March 20, 2026

Study Start

January 13, 2025

Primary Completion

May 31, 2025

Study Completion

October 31, 2025

Last Updated

March 20, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Locations