CompletedNot Applicable

In-person Focus Groups in the Management of Urinary Incontinence in Women

United States10 participantsStarted 2019-04-01

Plain-language summary

The purpose of this study is to investigate how a support group with other individuals who share the condition urinary incontinence (UI) impacts patients experience with management of urinary incontinence.

Who can participate

Age range18 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 18 years or older * English-speaking * Have the ability to commute to the meeting facility without institutional assistance Exclusion Criteria: • Those unable to attend all three focus group sessions

What they're measuring

Change in mixed urinary incontinence symptoms

Timeframe: Baseline, 12 weeks

Change in urinary distress

Timeframe: Baseline, 12 weeks

Change in overactive bladder satisfaction with treatment

Timeframe: Baseline, 12 weeks

Change in urinary tract condition severity

Timeframe: Baseline, 12 weeks

Change in urinary tract condition improvement

Timeframe: Baseline, 12 weeks

Change in sexual quality of life

Timeframe: Baseline, 12 weeks

Change in Patient Health Questionnaire

Timeframe: Baseline, 12 weeks

Change in physical activity

Timeframe: Baseline, 12 weeks

Trial details

NCT IDNCT05395793

SponsorMayo Clinic

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2019-09-29

View on ClinicalTrials.gov More Urinary Incontinence trials