- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07484373
Effects of Hip Abductor Strengthening Exercises in Patients With Piriformis Syndrome
Effects of Hip Abductor Strengthening Exercises on Pain, Range of Motion and Lower Extremity Function in Patients With Piriformis Syndrome
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Punjab Province
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Lahore, Punjab Province, Pakistan, 40100
- Hashir Ali clinic
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 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.
Exclusion Criteria:
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 .
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Arm 1: Hip Abductor Strengthening Exercise Group + conventional physiotherapy
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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 conventional Physiotherapy treatment
|
|
Active Comparator: Arm 2: Conventional Physiotherapy Group
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conventional Physiotherapy treatment
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Lower Extremity Functional Scale (LEFS)
Time Frame: From enrolment to the end of treatment at 4 weeks
|
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)
Time Frame: from enrollment to the end of treatment at 4 weeks
|
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 Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hip Abduction range of motion
Time Frame: from enrollment to the end of treatment.
|
Changes in hip abduction range of motion at baseline and 4 weeks of intervention were measured using a universal goniometer.
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from enrollment to the end of treatment.
|
|
Hip external roration ROM
Time Frame: From enrollment to the end of treatment at 4 weeks.
|
Changes in hip external rotation range of motion at baseline and 4 weeks of intervention were measured using a universal goniomete
|
From enrollment to the end of treatment at 4 weeks.
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Humera Mubashar, Ms-OMPT, Riphah 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
- REC/RCR & AHS/24/01113
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
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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