Tailoring Online Continence Promotion — TOCP  

Urinary Incontinence in Old Age Clinical Trial

Official title: Tailoring Online Continence Promotion for Women

Status Active, not recruiting

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. ;

Related Conditions & MeSH terms

• Fecal Incontinence
• Fecal Incontinence in Old Age
• Urinary Incontinence
• Urinary Incontinence in Old Age

• NCT number: NCT05183217
• Study type: Interventional
• Source: University of Wisconsin, Madison
• Status: Active, not recruiting
• Phase: N/A
• Start date: November 30, 2023
• Completion date: September 30, 2024