Autogenic vs. Reciprocal Inhibition Techniques for SI Joint Dysfunction
Official title: Comparative Effects of Autogenic Inhibition and Reciprocal Inhibition Technique on Pain, Functional Disability and Gait in Sacroiliac Joint Dysfuction.
Run by Foundation University Islamabad · NCT07600359 · Data updated 2026-11-12
The study tests two muscle-lengthening techniques (autogenic inhibition and reciprocal inhibition) to see if they reduce pain and improve function and walking in adults with sacroiliac joint dysfunction.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 25 Years to 45 Years |
| Sex | All |
| Enrollment | 40 (estimated) |
| Sponsor | Foundation University Islamabad Academic / other |
| Locations | 1 site (Islamabad, Punjab Province) |
| Status | Recruiting |
| Started | May 15, 2026 |
| Main results expected | July 1, 2026 |
| Study ends | July 15, 2026 |
| Registry record updated | May 20, 2026 |
| Trial ID | NCT07600359 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 25-45 with chronic (>4 weeks) sacroiliac joint-related low back pain and positive SIJ-related tests.
✕Probably not a fit
Patients with non-specific back pain, hip pathology, neurological issues, or those requiring assistive devices may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This interventional study compares two therapy approaches—autogenic inhibition and reciprocal inhibition—delivered over 12 sessions in 3 weeks. Participants have chronic low back pain due to sacroiliac joint dysfunction and will receive either autogenic inhibition of specific hip and back muscles with core stabilization, or reciprocal inhibition of those muscles with standard care. Both groups also receive conventional therapy and core stability exercises, with sessions including TENS and hot packs. Outcomes focus on pain, functional disability, and gait, using predefined clinical tests to confirm eligibility. The trial is conducted at Foundation University Islamabad with a single lead sponsor and no listed collaborators.
Why it matters
Potential benefit: If successful, patients may experience reduced pain and improved mobility and daily functioning.
How similar studies have gone: Previous work has explored similar muscle inhibition approaches, with some evidence of symptom improvement in related musculoskeletal conditions.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients having low back pain greater than 4 weeks * Patients with positive gaenslen's test, thigh thurst test, standing flexion test, sacral compression and distraction test. * Patients not having any other condition that can affect gait * 25-45 years * Both males and females Exclusion Criteria: * Patients having nonspecific low back * Patients with lumbosacral fusion * Patients with any neurological condition * Patients with history of trauma of spine * Patients with any other lumbar spine condition (lumbar radiculopathy, spinal stenosis, spondylolisthesis, inflammatory arthritis) * Patients with any hip joint pathology * Patients using any assistive device
Where it's running
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Foundation University College of Physical Therapy
Islamabad, Punjab Province, Pakistan Recruiting
Study contacts
- Principal investigator: Fajar Sajjad, DPT — Foundation University Islamabad
- Study coordinator: Fajar Sajjad, DPT
- Email: fajarsajjad1999@gmail.com
- Phone: 0331-5817637
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.