Clinical Trial

Effects of Core Stability and Pelvic Clock Exercises in Sacroiliac Joint Dysfunction

Recruiting
View on ClinicalTrials.gov →
Record status
This record was last updated June 10, 2026 (before its estimated July 1, 2026 completion). Its status may not reflect the trial's current state.
Summary
The study will be a randomized control trial and will be conducted in DHQ and Sadiq Hospital in Sargodha District. This study will be completed in time duration of 10 months after the approval of synopsis. Nonprobability convenience sampling technique will be used and 50 participants will be recruited in study after randomization. The subjects will be divided into two groups. Group A(Experimental) will receive core stability and pelvic clock exercises with baseline treatment while Group B(Control) will receive only core stability exercises after baseline treatment. The tools that will be used are Numeric Pain Rating Scale (NPRS), Oswestry Disability index (ODI) and WHOQOL-BREF. Treatment have duration of 8 weeks with 3 sessions per week and an hour per session is requires. After data collection, data will be analyzed by using SPSS version 26.
Protocol Amendment History 3 changes
critical Primary endpoint(s) modified 2026-06-11
notable Primary completion pushed: 2026-04 -> 2026-07-01 2026-06-11
minor Completion pushed: 2026-04 -> 2026-08-01 2026-06-11
Trial Details
NCT Number NCT07440849
Lead Sponsor Riphah International University
Conditions Sacroiliac Joint Dysfunction
Enrollment 50 participants
Start Date 2024-12-01
Primary Completion 2026-07-01 (estimated)
Study Completion 2026-08-01 (estimated)
Updated on ClinicalTrials.gov 2026-06-10