- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07661485
Comparing Two Soft Tissues Technique on Piriformis Syndrome Patients (MPR-PIR)
Effect of Myofascial Release as Compared to Post Isometric Relaxation in Improving Pain and Lower Extremity Function in Piriformis Syndrome
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Dr. Muhammad Muneeb Jafar, PhD Physiotherapy
- Phone Number: +923127000616
- Email: Muneebjafar.DPT@tuf.edu.pk
Study Contact Backup
- Name: Dr. Muhammad Ateeb, PhD Public Health
- Phone Number: +923357333383
Study Locations
-
-
Punjab Province
-
Faisalābad, Punjab Province, Pakistan, 38000
- The University of Faisalabad
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Positive Lasegue sign
- Positive FAIR test
- Grade 1-3 tenderness on palpation of piriformis between sacrum and greater trochanter of femur
- 4 or more pain intensity on the VAS scale
Exclusion Criteria:
Lower extremity injuries including ligament, tendon injuries, muscle strains as well as nerve injuries
- Systemic diseases including tuberculosis, multiple sclerosis, Parkinson's disease as well as chronic inflammatory conditions
- Congenital deformities including hip dysplasia, limb length discrepancy, scoliosis and congenital pelvic asymmetry
- Cognitive issues including dementia, severe depression and severe psychotic disorders
- Lumbar Radiculopathy
- SIJ Dysfunction
- Lower Extremity Fractures
- Pregnancy
- Malignancy
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: Myofascial release
Myofascial release was then performed with the patient positioned in prone lying.
The piriformis muscle was identified.
Sustained pressure was applied directly to the trigger point/piriformis muscle for 10-100 seconds while the patient actively moved the affected limb repeatedly from internal to external rotation.
Kneading strokes parallel to the muscle fibers were then performed for 5 minutes to promote elongation.
This sequence was repeated three times.
|
Myofascial release is performed with the patient positioned in prone lying.
The piriformis muscle was identified.
Sustained pressure was applied directly to the trigger point/piriformis muscle for 10-100 seconds while the patient actively moved the affected limb repeatedly from internal to external rotation.
Kneading strokes parallel to the muscle fibers were then performed for 5 minutes to promote elongation.
This sequence was repeated three times.
|
|
Experimental: Post Isometric Relaxation
The patient is in supine and the hip in neutral rotation. The affected hip was passively moved into horizontal adduction until a mild stretch was felt, while the lumbar spine was stabilized. The patient performed a gentle isometric contraction into hip abduction for 7-10 seconds, followed by 2-3 seconds of relaxation. The leg was then moved into further adduction to a new barrier. This contraction-relaxation-stretch cycle was performed for 3 sets of 5 repetitions. |
Post-isometric relaxation (PIR) is performed with the patient in supine and the hip in neutral rotation.
The affected hip was passively moved into horizontal adduction until a mild stretch was felt, while the lumbar spine was stabilized.
The patient performed a gentle isometric contraction into hip abduction for 7-10 seconds, followed by 2-3 seconds of relaxation.
The leg was then moved into further adduction to a new barrier.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Visual analogue scale
Time Frame: Baseline and 4 week post intervention
|
Comparison on effect of pain.
The Visual Analog Scale is a self-reported measure of pain intensity.
Participants rate their pain on a 10-cm scale ranging from 0 to 10, where 0 indicates "no pain" and 10 indicates "worst imaginable pain."
|
Baseline and 4 week post intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Lower Extremity Functional Scale
Time Frame: Baseline and 4 week of post intervention
|
Comparison on effect of functional outcomes.
The Lower Extremity Functional Scale (LEFS) is a self-reported questionnaire used to assess functional status and difficulty performing everyday activities in individuals with lower extremity musculoskeletal conditions.
The scale consists of 20 items, each scored from 0 to 4, yielding a total score ranging from 0 to 80.
|
Baseline and 4 week of post intervention
|
Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Ajimsha MS, Al-Mudahka NR, Al-Madzhar JA. Effectiveness of myofascial release: systematic review of randomized controlled trials. J Bodyw Mov Ther. 2015 Jan;19(1):102-12. doi: 10.1016/j.jbmt.2014.06.001. Epub 2014 Jun 13.
- This citation will not be hyperlinked on ClinicalTrials.gov. Aleem A, Arfan MT, Razzaq et al. (2022) Effectiveness of post isometric relaxation versus reciprocal inhibition technique on hamstring muscle flexibility. Annals of King Edward Medical University 28(2): 205-209.
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
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
- Pain
- Neurologic Manifestations
- Musculoskeletal Diseases
- Nervous System Diseases
- Neuromuscular Diseases
- Peripheral Nervous System Diseases
- Congenital Abnormalities
- Neuralgia
- Pelvic Pain
- Mononeuropathies
- Nerve Compression Syndromes
- Sciatic Neuropathy
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Pathological Conditions, Signs and Symptoms
- Signs and Symptoms
- Radiculopathy
- Musculoskeletal Abnormalities
- Sciatica
- Piriformis Muscle Syndrome
- Therapeutics
- Complementary Therapies
- Physical Therapy Modalities
- Rehabilitation
- Therapy, Soft Tissue
- Musculoskeletal Manipulations
- Massage
- Myofascial Release Therapy
Other Study ID Numbers
- TUF/EIRB/148/2025
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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