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

StatusRecruiting
PhaseNot applicable
Started2026-08-05
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary endpoint reworded 5 of 5 changed
See other at-risk trials from Mayo Clinic

Amendment history

2026-09-24
Primary endpoint(s) modified5 entries, revised
WasGlobal Rating of Change, ICIQ-UI, PFDI-20, Preferred Cadence, QUID
NowGlobal Rating of Change (GROC), International Consultation on Incontinence Questionnaire - Urinary Incontinence (ICIQ-UI), Preferred Cadence, Questionnaire for Female Urinary Incontinence Diagnosis (QUID), The Pelvic Floor Distress Inventory-20 (PFDI-20)
Mayo Clinic
1,015 trials monitored
See 115 trials at risk
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.
Trial Details
NCT Number NCT07829692
Lead Sponsor Mayo Clinic
Conditions Stress Urinary Incontinence
Enrollment 66 participants
Start Date 2026-08-05
Primary Completion 2029-08-05 (estimated)
Study Completion 2029-08-05 (estimated)
Updated on ClinicalTrials.gov 2026-09-23