Accelerometer Measured Early Recovery After Prolapse Surgery
Recruiting
N/A
Interventional Study
Pelvic Organ Prolapse
Pelvic Organ Prolapse (POP)
Pelvic Organ Prolapse Vaginal Surgery
Pelvic Organ Prolapse, Patient Education
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 99
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 288 (estimated)
- Sponsor
- NICHD Pelvic Floor Disorders Network · Research network
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About This Trial
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 …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Subject has provided written informed consent
* Ambulatory women undergoing laparoscopic, robotic, or vaginal reconstructive or obliterative surgery for apical prolapse
* POP-Q \>= Stage III
* Willing to participate in a postoperative exercise regimen
* Able to read and consen…
Contacts
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