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Accelerometer Measured Early Recovery After Prolapse Surgery

Study acronym: AccelERate
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

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  1. Primary completion moved earlier from Mar 31, 2028 to Jun 30, 2027
    • Study completion moved earlier from Dec 31, 2028 to Mar 31, 2028
    v5
  2. Secondary endpoints: details revised at 1 of 9 entries
    • Study description shortened, about 5 words
    • Study title expanded, about 4 words
    v4
  3. Study sites: 6 to 7v3
  4. Site details revised at 4 of 6 sitesv2
  5. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 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.
Trial Details
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
(from sponsor)		 Pelvic Organ Prolapse, Pelvic Organ Prolapse (POP), Pelvic Organ Prolapse Vaginal Surgery, Pelvic Organ Prolapse, Patient Education
Related terms Pelvic Organ Prolapse
Enrollment 288 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov