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Clinical Trial Summary

This project seeks to understand whether, and how, tailoring an online continence intervention can increase engagement and uptake of health behaviors known to improve bladder and bowel symptoms.


Clinical Trial Description

The investigators will conduct a two-arm, parallel, randomized, controlled trial (RCT) comparing an online continence promotion program with standard weekly reminders (control arm) to an online continence promotion program with tailoring (treatment arm) to determine the impact of tailoring on program engagement. Women in the treatment arm will receive tailored content and digital reminders for 24 weeks based on their individual characteristics, symptoms, and behaviors assessed at baseline, with reassessment of key inputs every 2 weeks resulting in re-tailored outputs. Participants will complete electronic surveys at enrollment, 4, 12, and 24 weeks. To contextualize the findings from all 3 aims, a subset of participants will be invited to complete semi-structured qualitative interviews about their engagement with the program, their adoption of health behaviors, and their perceived barriers to and facilitators of engagement and behavior change. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05183217
Study type Interventional
Source University of Wisconsin, Madison
Contact Madeline K Moureau, BS
Phone 608-417-6493
Email [email protected]
Status Not yet recruiting
Phase N/A
Start date June 2022
Completion date February 2024

See also
  Status Clinical Trial Phase
Completed NCT04036604 - Investigation of The Effect of Pelvic Floor Exercise Programme in Elderly. N/A
Suspended NCT04297904 - Urinary Incontinence and Sedentary Behaviour in Nursing Homes
Completed NCT03176901 - Comparing Approaches to Treat Older Adult Women's Urge Incontinence: Pilot Feasibility and Randomized Controlled Trial N/A
Completed NCT03140852 - Community-Based Continence Promotion: Sustaining Healthy Aging in Place (SHAIP) Through Mind Over Matter (MOM) N/A