Comparing two muscle energy techniques for treating iliotibial band syndrome
Comparison of Effects of Autogenic Inhibition and Reciprocal Inhibition Muscle Energy Techniques on Iliotibial Band Syndrome
NA · Foundation University Islamabad · NCT06867159
This study is testing two different muscle techniques to see which one helps people with iliotibial band syndrome feel less pain and move better.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 19 Years to 45 Years |
| Sex | All |
| Sponsor | Foundation University Islamabad (other) |
| Locations | 1 site (Rawalpindi, Punjab Province) |
| Trial ID | NCT06867159 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to compare the effects of autogenic inhibition and reciprocal inhibition muscle energy techniques on patients suffering from iliotibial band syndrome. It will be a single-blinded randomized control trial conducted over one year at Foundation University Islamabad, involving 40 participants divided into two groups. Each group will perform their assigned technique three times a week for two weeks, with outcomes measured in terms of pain reduction, hip range of motion, and lower extremity function. Assessments will utilize the Numeric Pain Rating Scale, goniometer, and Lower Extremity Functional Scale.
Who should consider this trial
Good fit: Ideal candidates are males and females aged 19-45 with lateral knee pain lasting more than three months and specific tenderness and positive test results.
Not a fit: Patients with recent lower limb surgeries, fractures, or significant structural disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide effective non-invasive treatment options for patients with iliotibial band syndrome.
How similar studies have performed: While similar muscle energy techniques have been explored, this specific comparison of autogenic versus reciprocal inhibition is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria * Both male and female participants * Age : 19-45years (8) * Lateral knee pain (\>3 months) * Tenderness over lateral femoral condyle * Positive Flexibility Tests * Modified Ober's test (9) * Length assessment of Tensor Fasciae Latae and Iliotibial Band (10) * Positive Pain Provocation Tests * Renne's test * Noble's Compression test (11) \*(individuals with 3 positive tests out of above mentioned 4 tests will be included) Exclusion Criteria * Recent lower limb or pelvic girdle surgery within the past 3 months * Lower limb fractures or trauma within the past year. * Multiple lower limb surgeries (\>2) * Presence of any structural or postural disorders (kyphosis or severe scoliosis) * Neurological disorders * Hip and knee Osteoarthritis * Rheumatoid Arthritis * Pregnancy
Where this trial is running
Rawalpindi, Punjab Province
- Foundation University College of Physcial Therapy — Rawalpindi, Punjab Province, Pakistan (RECRUITING)
Study contacts
- Study coordinator: Rida Ishtiaq, MS-MSKPT*
- Email: ridaishtiaq777@gmail.com
- Phone: 03365530415
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.
Conditions: Iliotibial Band Syndrome