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Effects of Corrective Versus Plank Exercises on Diastasis Recti

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

See every version on ClinicalTrials.gov ↗

  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 12 words
    • Publications: details revised at 5 of 6 entries
  2. Primary completion pushed from Apr 1, 2026 to Jul 1, 2026
    • Study completion pushed from May 1, 2026 to Aug 1, 2026
    v3
  3. Primary completion pushed from Feb 2026 to Apr 1, 2026
    • Study completion pushed from Mar 1, 2026 to May 1, 2026
    v2
  4. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
This study will be randomized clinical trial and will be conducted in Services Hospital and poly clinics. The total duration of treatment will be 12 weeks. Non-probability convenience sampling technique will be used and 56 participants will be recruited in study after randomization. The participants are randomly assigned to one of two groups: Group A performs corrective exercises focused on deep core engagement, while Group B performs plank exercises aimed at overall abdominal activation. Each group follows their respective regimen three times per week for 12 weeks. Baseline EMS and pelvic floor exercises are conducted for all participants to ensure core stability before the interventions begin. Outcome measures, including manual muscle testing (MMT) for strength, and the Numerical Pain Rating Scale (NPRS) for pain, are recorded both before and after the 12-week intervention. After data collection data will be analyzed by using SPSS version 25.
Trial Details
NCT Number NCT07440836
Lead Sponsor Riphah International University
Conditions
(from sponsor)		 Diastasis Recti
Related terms Pain
Enrollment 56 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov