Geneva, Sept. 25 -- International Clinical Trials Registry received information related to the study (NCT07829692) titled 'Effectiveness of an 8-week Independent Cadence Retraining Program on Stress Urinary Incontinence in Parous Runners: A Randomized Controlled Trial' on Sept. 15.

Study Type: Interventional

Study Design: Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: None (Open Label).

Primary Sponsor: Mayo Clinic

Condition: Stress Urinary Incontinence

Intervention: Other: Cadence Increase

Recruitment Status: Recruiting

Phase: N/A

Date of First Enrollment: August 5, 2026

Target Sample Size: 66

Countries of Recruitment: United States

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