Effectiveness of an 8-week Independent Cadence Retraining Program on Stress Urinary Incontinence in Parous Runners.

Part of paid clinical trials in Rochester, Minnesota.

Sponsor
Mayo Clinic
Study ID
NCT07829692
Status
Recruiting
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Conditions

  • Stress Urinary Incontinence

Eligibility Criteria

Sex
FEMALE
Age
18 Years - N/A
Healthy Volunteers
Accepted

Interventions

  • Cadence Increase — OTHER
    Utilizing cadence alarm on a garmin device, the intervention group will attempt to increase their running cadence by 10%.
  • Cadence Maintenance — OTHER
    Participants will use cadence alarms to maintain preferred running cadence.

Study Details

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.

Key Dates

First listed
Sep 21, 2026
Start date
Aug 5, 2026
Status verified
Sep 2026
Primary completion
Aug 5, 2029
Completion
Aug 5, 2029

Study Design

Enrollment
66 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Cadence increase group
    Participants will log running data and set cadence alarms to increase running cadence by 10%
  • Placebo Comparator: Cadence Maintenance Arm
    Participants will log their running data and set cadence alarm to maintain cadence.

Primary Outcome Measure

Preferred Cadence [ Time Frame: Baseline and 8 weeks ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Mayo ClinicRochesterMinnesota55905
Sally Olmstead
[email protected]
316-641-6192
Nicole Ron
[email protected]
505-480-4548

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