Overview
This is a study evaluating a novel active recovery program in the immediate postoperative period following pelvic reconstructive surgery.
Description
This is a randomized controlled trial comparing usual care postoperative restrictions and a novel new active recovery program to look at differences in pelvic floor function, patient quality of life, and mental health in between groups.
Eligibility
Inclusion Criteria:
- Between the ages of 18 and 89
- Undergoing minimally invasive apical prolapse reconstructive procedure at OHSU. This includes laparoscopic and robotic-assisted sacrocolpopexy, laparoscopic and vaginal uterosacral ligament suspension, and vaginal sacrospinous ligament fixation. We will include patients undergoing concomitant procedures such as hysterectomy and incontinence procedures.
- Have access to reliable email for communication and questionnaires.
Exclusion Criteria:
- Unable to consent
- Unable to read and complete questionnaires in English
- Unable to sustain 30 minutes of moderate walking/activity at baseline (self-reported)
- Use a mobility assistance device such as a walker/cane at baseline
- Balance or stability problems
- Patients on chronic opioids