Reducing Chronic Pain Following Cesarean Delivery

StatusRecruiting
PhaseNot applicable
Started

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Trial flagged as At Risk
Primary completion moved at least 31 days later Dec 31, 2026 → Jan 31, 2027
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Record History

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  1. Recruitment opened
    • Site details revised
  2. Re-verified, no change to tracked fields
  3. Primary completion pushed from Dec 31, 2026 to Jan 31, 2027
    • Study completion pushed from Jan 26, 2027 to Mar 14, 2027
    • Start date pushed from Sep 15, 2026 to Oct 5, 2026
    • Secondary endpoints revised (10)
  4. Study First Submitted
  • 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 pilot study will evaluate the feasibility and acceptability of delivering Empowered Relief (ER), a single-session pain relief skills class, to postpartum women with ongoing pain and/or pain interference following cesarean delivery. Participants will receive ER in addition to standard postpartum care and will be followed through 12 weeks postpartum.
Trial Details
NCT Number NCT07799883
Lead Sponsor Stanford University
Collaborators: Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institute on Drug Abuse (NIDA)
Conditions
(from sponsor)		 Chronic Pain, Cesarean Section Complications, Postpartum
Related terms Agnosia, Chronic Pain, Postoperative Pain
Enrollment 30 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov