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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

Sponsor: Mayo Clinic · Participants: 66 · Started: Aug 5, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07829692

Locations in the U.S.

MinnesotaMayo Clinic, Rochester

Conditions

From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.