Accelerometer Measured Early Recovery After Prolapse Surgery

The AccelERate study will evaluate the physical recovery of patients who have undergone Pelvic Organ Prolapse (POP) surgery. This will be evaluated via a self-reported recovery questionnaire completed daily. Participants will wear an accelerometer device on their non-dominant wrist and be given either routine or exercise-focused postoperative instructions. The primary outcome will be a comparison of the number of days needed to reach self-reported "mostly recovered" status between randomly assigned instruction groups.

NCT Number	NCT07218016
Lead Sponsor	NICHD Pelvic Floor Disorders Network Collaborators: RTI International, University of California, San Diego, University of Chicago, Duke University, Women and Infants Hospital of Rhode Island, University of Pennsylvania, Kaiser Permanente, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Conditions	Pelvic Organ Prolapse, Pelvic Organ Prolapse (POP), Pelvic Organ Prolapse Vaginal Surgery, Pelvic Organ Prolapse, Patient Education
Enrollment	288 participants
Start Date	2025-10-02
Primary Completion	2027-06-30 (estimated)
Study Completion	2028-03-31 (estimated)
Updated on ClinicalTrials.gov	2026-04-27