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Postoperative Active Recovery

Oregon Health & Science University (OHSU) logo

Oregon Health & Science University (OHSU)

Status

Completed

Conditions

Pelvic Floor Disorders

Treatments

Other: Active Recovery
Other: Standard of Care

Study type

Interventional

Funder types

Other

Identifiers

NCT05950633
OHSU IRB 25625

Details and patient eligibility

About

This is a study evaluating a novel active recovery program in the immediate postoperative period following pelvic reconstructive surgery.

Full 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.

Enrollment

72 patients

Sex

Female

Ages

18 to 89 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Between the ages of 18 and 89
  2. 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.
  3. Have access to reliable email for communication and questionnaires.

Exclusion criteria

  1. Unable to consent
  2. Unable to read and complete questionnaires in English
  3. Unable to sustain 30 minutes of moderate walking/activity at baseline (self-reported)
  4. Use a mobility assistance device such as a walker/cane at baseline
  5. Balance or stability problems
  6. Patients on chronic opioids

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

72 participants in 2 patient groups

Standard of Care
Active Comparator group
Description:
Participants will receive standard postoperative instructions only
Treatment:
Other: Standard of Care
Active Recovery
Active Comparator group
Description:
Participants will receive active recovery instructions with specific walking goals, abdominal strengthening exercises, and pelvic floor exercises
Treatment:
Other: Active Recovery

Trial contacts and locations

1

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Central trial contact

Women's Health Research Unit Department of Ob/Gyn

Data sourced from clinicaltrials.gov

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