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

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 3 months later Jul 1, 2026 → Oct 2026
See other at-risk trials from Riphah International University

Record History

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  1. Primary completion pushed from Jul 1, 2026 to Oct 2026
    • Study completion pushed from Aug 1, 2026 to Oct 2026
    • Eligibility criteria expanded, about 9 words
    • Publications: details revised at 4 of 5 entries
  2. Primary endpoint(s) modified
    • Primary completion pushed from Apr 2026 to Jul 1, 2026
    • Study completion pushed from Apr 2026 to Aug 1, 2026
    v2
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT07440849
Lead Sponsor Riphah International University
Conditions
(from sponsor)		 Sacroiliac Joint Dysfunction
Enrollment 50 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov