- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07646314
Comparative Effects of Post-Isometric Relaxation and Reciprocal Inhibition Techniques inPiriformis Syndrome
Comparative Effects of Post-Isometric Relaxation and Reciprocal Inhibition Muscle Energy Techniques on Pain, ROM and Function in Piriformis Syndrome
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Imran Amjad
- Phone Number: 03324390125
- Email: Imran.amjad@riphah.edu.pk
Study Locations
-
-
Punjab Province
-
Lahore, Punjab Province, Pakistan, 54000
- Ghurki Hospital Lahore
-
Contact:
- Hira Shaukat, TDPT
- Phone Number: 03360405480
- Email: hira.shaukat@riphah.edu.pk
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Principal Investigator:
- Hafiza Mahnoor Anwar, MSOMPT
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Piriformis syndrome clinically confirmed via special tests (e.g., FAIR test, Freiberg sign, Pace test)
- Both gender male and female.
- Age between 25 and 40 years.
- Presence of antalgic gait due to pain.
- Moderate to severe pain (e.g., NPRS score ≥ 4)
- Voluntary consent to participate in the study.
- Medically stable, no acute or unstable medical conditions that would interfere with participation.
Exclusion Criteria:
Lumber disc herniation or radiculopathy confirmed by imaging or neurological signs
- History of hip or pelvis surgery.
- Other neuromuscular or musculoskeletal disorders e.g., stroke, multiple sclerosis, or rheumatoid arthritis
- Recent lower limb fracture or injury within the last 6 months.
- Pregnancy due to potential risks and altered biomechanics.
- Inability to follow instruction
- Ongoing physiotherapy or alternative treatments
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: Post isometrics Relaxation Techniques (PIR)
In this group First conventional treatment will be applied for 20 minutes including Hot Pack and TENS (for 15 minutes) and sonics (for 5 minutes) Followed by PIR.
|
Post-Isometric Relaxation is a type of MET in which the target muscle is gently contracted isometrically (without movement) against resistance, followed by a passive stretch during the post-contraction relaxation phase. To reduce muscle tension, increase flexibility, and lengthen tight muscles (like the piriformis in Piriformis Syndrome). Position the patient in a stretch position for the tight muscle just before the point of resistance. Then ask the patient to perform a gentle isometric contraction of the tight muscle (e.g., piriformis) for about 5-10 seconds against minimal resistance. After contraction, the patient relaxes for a few seconds. During this relaxation, the therapist passively stretches the muscle to a new barrier and holds for 15-30 seconds. Repeat 3-5 times. So, the whole treatment session will be of 50 minutes. This technique will be applied twice a week for 4 weeks. |
|
Active Comparator: Reciprocal Inhibition Technique
This group will receive Hot Pack and TENS (for 15 minutes) and Sonics (for 5 minutes) Followed by METs.
|
Reciprocal Inhibition is another MET technique where the antagonist of the tight muscle is contracted, which reflexively causes the tight (agonist) muscle to relax.
To inhibit the overactive muscle by activating its opposing muscle group, allowing for greater stretch and flexibility.
Place the muscle (e.g., piriformis) into a gentle stretch.
Ask the patient to contract the antagonist muscle (e.g., hip adductors/internal rotators) for about 5-10 seconds.
Therapist then passively stretches the target muscle (e.g., piriformis) further.
Repeat 3-5 times.
So, the whole treatment session will be of 50 minutes.
This technique will be applied twice a week for 4 weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
NPRS for assessment of pain
Time Frame: 4 weeks
|
To determine the degree of pain that the patient will report, the Numeric Pain Rating Scale (NPRS) will be utilized.
|
4 weeks
|
|
Lower Extremity Function Test (LEFT)
Time Frame: 4 weeks
|
The LEFT protocol includes a timed sequence of agility-based tasks, typically performed in a zigzag pattern or shuttle-based layout over a 120-foot course
|
4 weeks
|
|
GONIOMETERY
Time Frame: 4 weeks
|
Goniometry is the measurement of joint angles in the human body using a tool called a goniometer.
It is a standard and essential part of physical therapy and rehabilitation for assessing range of motion (ROM) in various joints
|
4 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Hira Shaukat, Mphill, Riphah International University
Publications and helpful links
General Publications
- Boyajian-O'Neill LA, McClain RL, Coleman MK, Thomas PP. Diagnosis and management of piriformis syndrome: an osteopathic approach. J Am Osteopath Assoc. 2008 Nov;108(11):657-64. doi: 10.7556/jaoa.2008.108.11.657.
- Kean Chen C, Nizar AJ. Prevalence of piriformis syndrome in chronic low back pain patients. A clinical diagnosis with modified FAIR test. Pain Pract. 2013 Apr;13(4):276-81. doi: 10.1111/j.1533-2500.2012.00585.x. Epub 2012 Aug 2.
- Kutty NN, Siddeeque S, Tamphaibema H, Othayoth N, Bineesh C. Effect of Muscle Energy Technique with Deep Friction Massage on Pain, Disability and Internal Rotation Range of Motion of Hip Joint in Individuals with Piriformis Syndrome. Indian Journal of Physiotherapy & Occupational Therapy. 2020;14(1).
- Tonley JC, Yun SM, Kochevar RJ, Dye JA, Farrokhi S, Powers CM. Treatment of an individual with piriformis syndrome focusing on hip muscle strengthening and movement reeducation: a case report. J Orthop Sports Phys Ther. 2010 Feb;40(2):103-11. doi: 10.2519/jospt.2010.3108.
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
Other Study ID Numbers
- REC/RCR&AHS/25/0120
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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