Comparing two muscle energy techniques for treating Piriformis Syndrome
Comparative Effects of Autogenic Inhibition and Reciprocal Inhibition Muscle Energy Techniques in Piriformis Syndrome
This study is testing two different muscle treatment techniques to see which one helps people with Piriformis Syndrome feel better.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 32 (estimated) |
| Ages | 25 Years to 45 Years |
| Sex | All |
| Sponsor | Riphah International University Academic / other |
| Locations | 1 site (Rawalpindi, Punjab Province) |
| Trial ID | NCT06460675 on ClinicalTrials.gov |
What this trial studies
This study investigates the effectiveness of two different Muscle Energy Techniques (METS) - Autogenic Inhibition and Reciprocal Inhibition - in treating patients with Piriformis Syndrome. The trial will involve 32 participants aged 25-45, who will be randomly assigned to one of the two treatment groups. Each participant will undergo six sessions of their assigned technique over three weeks, with follow-up assessments to evaluate pain, range of motion, and disability. The goal is to determine which technique is more effective in alleviating symptoms associated with this condition.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 25-45 diagnosed with Piriformis Syndrome and experiencing moderate hip pain.
Not a fit: Patients with hip degenerative changes, trauma history, or other systemic conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide patients with a more effective treatment option for managing Piriformis Syndrome.
How similar studies have performed: While there is limited data on the specific comparison of these two techniques, similar approaches in muscle energy techniques have shown promise in treating musculoskeletal conditions.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Both genders with ages between 25-45 years. * Patients diagnosed with Piriformis syndrome using the Piriformis FAIR test, Freiberg test, Lasegue test, Beaty test, and pace sign. * Hip pain with a threshold of NPRS 3-6. * Limited ROM of Hip Internal Rotation and Abduction measured using a goniometer. * Buttock pain ≥ 3 months. * Pain with prolonged sitting (more than 20 minutes) Exclusion Criteria: * Hip Degenerative changes. * History of Trauma or Fracture * Other Systemic Conditions * Postural abnormality/deformity * Diagnosed Psychological Disorders * Pregnancy
Where this trial is running
Rawalpindi, Punjab Province
- IIMCT Railway General Hospital — Rawalpindi, Punjab Province, Pakistan (Recruiting)
Study contacts
- Principal investigator: Rabiya Noor, PhD — Riphah International University
- Study coordinator: Mateen Asghar, MS-DPT
- Email: mateen04443@gmail.com
- Phone: 03046368317
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.