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Gong's Mobilization and Jone's Positional Release for SIJ Dysfunction

Comparing The Effects of Gong's Mobilization and Jone's Positional Release for Sacroiliac Joint Dysfunction.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07580430
Enrollment
30
Registered
2026-05-12
Start date
2025-08-01
Completion date
2026-04-30
Last updated
2026-05-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sacro Iliac Joint Pain, Sacroiliac Disorder, Sacroiliac Joint Dysfunction

Keywords

sacroiliac arthritis, sacroiliitis, physical therapy, Gong's mobilization

Brief summary

This study aims to compare the efficacy of Gong's mobilization and Jones's positional release technique in individuals with sacroiliac joint dysfunction.

Detailed description

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.

Interventions

A pain-free, sustained glide is applied to the sacroiliac joint by the therapist. The patient simultaneously performs active movements.

OTHERJone's positional release

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.

Sponsors

Elite College of Management Sciences, Gujranwala, Pakistan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Positive provocation tests * Low Back and Buttocks pain for more than 3 months * Oswestry score of atleast thirty percent

Exclusion criteria

* Spinal fracture * Lower extremity fracture * surgery * pregnancy * spinal deformity

Design outcomes

Primary

MeasureTime frameDescription
Modified Oswestry Low Back Pain Disability Questionnaire6 weeksThe 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.
Visual Analogue Scale6 weeksThe 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.

Countries

Pakistan

Contacts

STUDY_DIRECTORSyeda Mahnoor Hassan, MS Physical Therapy

Elite College of Management Sciences, Gujranwala

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 15, 2026