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Effectiveness of an 8-week Independent Cadence Retraining Program on Stress Urinary Incontinence in Parous Runners.
RecruitingHealthy volunteers welcome
Effectiveness of an 8-week Independent Cadence Retraining Program on Stress Urinary Incontinence in Parous Runners: A Randomized Controlled Trial.
Who can join
Ages 18 and older · Women · Healthy volunteers welcome
Full eligibility criteria
Inclusion Criteria: * Healthy * Nonpregnant * Female volunteers * Self-reported urinary incontinence during running with history of at least one prior delivery after 32 weeks gestation and who run 6 miles/week with a preferred cadence of less than or equal to 170 steps per minute determined via personal report from current Garmin watch data. * Participants must own their own or have access to a Garmin watch. * Participants must read, speak, and understand English sufficiently to provide informed consent and complete study procedures and questionnaires. Exclusion Criteria: * Unwillingness to complete all components of the study * Urge only urinary incontinence * \<3 months postpartum or current pregnancy * History of prolapse repair or incontinence surgery * Participants will also be excluded if they do not own or utilize a Garmin watch that provides cadence assessment and alarm.
About the study
The purpose of this research is to assess the impact of an eight-week home cadence training program on stress urinary incontinence symptoms in parous women.
What is being tested
- Cadence Increase (other)
- Cadence Maintenance (other)
Sponsor: Mayo Clinic · Participants: 66 · Started: Aug 5, 2026
Contact the study team
- Sally Olmstead · Phone: 316-641-6192
Official record on ClinicalTrials.gov — NCT07829692
Locations in the U.S.
| Minnesota | Mayo Clinic, Rochester |
Conditions
From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.