Accelerometer Measured Early Recovery After Prolapse Surgery (NCT07218016)
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: Review the eligibility criteria below.
Location: Kaiser Permanente -- San Diego — San Diego, California
Age range: 18 Years to 99 Years
🧪 Interventions in This Study
- Postoperative Exercise regimen (BEHAVIORAL)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (7 Sites)
- Kaiser Permanente -- San Diego — San Diego, California
- University of California - San Diego — San Diego, California
- University of Chicago — Chicago, Illinois
- Duke University, Duke Division of Urogynecology and Reconstructive Pelvic Surgery — Durham, North Carolina
- University of Pennsylvania — Philadelphia, Pennsylvania
- Brown/ Women and Infants Hospital of Rhode Island, Division of Urogynecology and Reconstructive Pelvic Surgery — Providence, Rhode Island
- University of Texas Southwestern Medical Center — Dallas, Texas
📞 Contact the Study Coordinator
Phone: (619) 221-6274
Email: Gisselle.Zazueta-Damian@kp.org
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Pelvic Organ Prolapse
- POMEGRANATE Trial: Comparing Reia Pessary Versus Standard of Care Pessary for Pelvic Organ Prolapse Treatment — Birmingham, Alabama
- Intraoperative Costs and Patient Perceptions in Sacrocolpopexy for Prolapse — Rochester, Minnesota
- Composite Outcomes of Mesh vs Suture Techniques for Prolapse Repair: A Randomized Controlled Multicentre Trial — Vancouver, British Columbia
- Vaginal Orthosis Use After Vaginal Reconstructive Surgery — Birmingham, Alabama
- Platelet Rich Plasma as an Adjunct Therapy at the Time of Transvaginal Native Tissue Prolapse Surgery — Birmingham, Alabama
- Pessary Experience Study — Charlottesville, Virginia
Explore by condition: All Pelvic Organ Prolapse clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.