Comparing two stretching techniques for treating Quadratus Lumborum Syndrome
Comparison of Post Facilitation Stretch Versus Reciprocal Inhibition in Quadratus Lumborum Syndrome: a Randomized Controlled Trial
This study is testing two different stretching techniques to see which one helps young adults with chronic pain from Quadratus Lumborum Syndrome feel better.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 42 (estimated) |
| Ages | 18 Years to 35 Years |
| Sex | All |
| Sponsor | Foundation University Islamabad Academic / other |
| Locations | 1 site (Rawalpindi, Punjab Province) |
| Trial ID | NCT06534853 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to compare the effectiveness of Post Facilitation Stretch versus Reciprocal Inhibition in patients suffering from Quadratus Lumborum Syndrome. Participants aged 18-35 with chronic pain will be randomly assigned to one of two groups, with both receiving conventional physical therapy. Group A will undergo Post Facilitation Stretch, while Group B will receive Reciprocal Inhibition. Pain levels, lumbar range of motion, leg length discrepancy, and lumbar lordotic angle will be measured before and after the interventions to assess outcomes.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 18-35 experiencing chronic pain related to Quadratus Lumborum Syndrome.
Not a fit: Patients with conditions such as radiculopathy, previous lower limb surgeries, or those who are pregnant or lactating may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide patients with more effective treatment options for managing pain and improving mobility associated with Quadratus Lumborum Syndrome.
How similar studies have performed: While similar approaches have been explored, this specific comparison of Post Facilitation Stretch and Reciprocal Inhibition in Quadratus Lumborum Syndrome is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age 18-35 years * Both genders * Having pain of ≤ 8 on NPRS from at least 3 months * Pain decreases on supine lying * Any two of the following findings positive of unilateral quadratus lumborum on physical examination: 1. Taut bands 2. Local tenderness 3. Patient's pain recognition 4. Pain referral to greater trochanter 5. Local twitch response Exclusion criteria: * Painful isometric muscle testing of hip flexors, abductors, adductors, and extensors * Previous surgery of lower limb * Centralization/peripheralization * Lower back trauma * Positive SLR * Radiculopathy * Fracture/surgery of pelvic and/or hip region * Diagnosed fibromyalgia or other rheumatic diseases. * Lactating women * Intrauterine device * Pregnant women * Use of psychiatric medications
Where this trial is running
Rawalpindi, Punjab Province
- Foundation University College of Physical Therapy — Rawalpindi, Punjab Province, Pakistan (Recruiting)
Study contacts
- Study coordinator: Aqsa Ayaz, MS-MSKPT*
- Email: aqsaayaz77@gmail.com
- Phone: 03365765782
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.