Effectiveness of an 8-week Independent Cadence Retraining Program on Stress Urinary Incontinence in Parous Runners.
Effectiveness of an 8-week Independent Cadence Retraining Program on Stress Urinary Incontinence in Parous Runners: A Randomized Controlled Trial.
- Stress Urinary Incontinence
At a glance
- Phase
- Phase not stated
- Study type
- Interventional
- Sponsor
- Mayo Clinic
- Enrolment target
- 66
- Started
- 5 August 2026
- Main results due
- 5 August 2029
- Study sites
- 1
- Registry updated
- 23 September 2026
Can you take part?
- Aged 18 years and over.
- Women only.
- Healthy volunteers can take part.
These are the headline rules only. Every study has a longer list, and whether you are eligible is decided by the research team at the site — never by this page.
Read the 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.
What this study is about
In the sponsor’s own words, from the registry.
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.
Study sites(1)
Mayo Clinic
Rochester, Minnesota, United States
Recruiting
Showing 1 of 1 sites. 1 of the 1 site on this study is recruiting right now — a site can stop enrolling while the study as a whole is still open.
Source: ClinicalTrials.gov record NCT07829692. Trialion does not run this study, is not paid to refer anyone to it, and cannot enrol you. Eligibility is always decided by the research team at the site.
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