Home › Pelvic Floor Disorders › NCT02316275
Impact of Unrestrictive Exercise Following Mid-Urethral Sling Surgery
IMpact of Unrestricted ACTIVity Following Mid-Urethral Sling Surgery (I'M ACTIVe): Quality of Life and Cost Implications
Who can join
Ages 18 and older · Women
Full eligibility criteria
Inclusion Criteria: * Non-pregnant female * Self-reported stress urinary incontinence * Incontinence demonstrated on physical exam and/or by an urodynamics study * Planned mid-urethral sling surgery * Available for 2 years of follow-up * Willing and able to complete study assessments per the judgment of the treating clinician * Willing and able to provide written informed consent Exclusion Criteria: * Age \<18 years at time of enrollment * Concomitant prolapse surgery other than anterior colporrhaphy * Currently pregnant or \<12 months post-partum * Unable to read, write, or comprehend English
About the study
To determine the impact of unrestricted postoperative activity on intermediate- and long-term continence outcomes of mid-urethral sling surgery in women with stress urinary incontinence.
To assess the natural return to baseline activity level when patients are unrestricted following mid-urethral sling surgery with or without concomitant anterior or posterior pelvic organ prolapse repair.
What is being tested
- No post-operative activity restrictions (other)
- Standard post-operative activity restriction (other)
Sponsor: Cedars-Sinai Medical Center · Participants: 50 · Started: 2011-12
Contact the study team
- Jennifer Anger, MD, MPH · Phone: 3103852992
Official record on ClinicalTrials.gov — NCT02316275
Locations in the U.S.
| California | Cedars-Sinai Medical Center, Beverly Hills |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.