An interventional study of Gong's mobilization and Jone's positional release in Sacro Iliac Joint Pain, Sacroiliac Disorder and Sacroiliac Joint Dysfunction, sponsored by Elite College of Management Sciences, Gujranwala, Pakistan. Completed at 1 site in Pakistan. Per ClinicalTrials.gov, last updated 2026-05-14.
Sponsored by Elite College of Management Sciences, Gujranwala, Pakistan · Not applicable, Interventional, and Treatment
This study aims to compare the efficacy of Gong's mobilization and Jones's positional release technique in individuals with sacroiliac joint dysfunction.
The study was designed as a randomized controlled trial involving 30 participants diagnosed with sacroiliac joint dysfunction. Participants were randomly divided into two equal groups of 15 using a lottery method. Group A underwent Gong's mobilization, whereas Group B received Jones's positional release technique. In addition, both groups were provided with baseline treatment, including TENS and stretching exercises. Each intervention was carried out three times per week for a duration of six weeks.
42 studies on the registry are indexed under Sacroiliitis; 11 are open to participants now.
This study's enrollment of 30 is below the median of 48 across 28 interventional studies indexed under Sacroiliitis.
Browse Sacroiliitis studies →Elite College of Management Sciences, Gujranwala, Pakistan is the lead sponsor of 17 studies on the registry; none are open to participants now.
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Exclusion Criteria:
A pain-free, sustained glide is applied to the sacroiliac joint by the therapist. The patient simultaneously performs active movements.
Other: Gong's mobilization
The therapist identifies a tender point. The patient is positioned in a way that reduces pain significantly. This position is held for about 90 seconds and the patient is then slowly returned to a neutral position.
Other: Jone's positional release
A pain-free, sustained glide is applied to the sacroiliac joint by the therapist. The patient simultaneously performs active movements.
The therapist identifies a tender point. The patient is positioned in a way that reduces pain significantly. This position is held for about 90 seconds and the patient is then slowly returned to a neutral position.
Modified Oswestry Low Back Pain Disability Questionnaire
The Modified Oswestry Low Back Pain Disability Questionnaire is a gold-standard tool used to measure a patient's functional disability level resulting from low back pain.
Time frame: 6 weeks
Visual Analogue Scale
The Visual Analogue Scale (VAS) is used to measure pain intensity. The VAS typically consists of a 100 mm (10 cm) horizontal line where zero means no pain and ten indicates worst possible pain.
Time frame: 6 weeks
Plan to share: No
This study is completed, as verified in May 2026. You cannot join it, but the record below documents what was studied.
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Elite College of Management Sciences, Gujranwala, Pakistan