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Clinical Trial Summary

To determine whether women exposed to the continence promotion intervention will report improved urinary symptoms and quality of life, and lower incontinence-related stigma and falls than women who receive a control intervention at one-year post-intervention.


Clinical Trial Description

This is a cluster-randomized 4-site intervention study testing the effect of a continence-promotion intervention on:

1. Improved urinary symptoms and quality of life

2. Reduction in falls

3. Reduction in stigma

A cost-effectiveness component will also be included ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01858493
Study type Interventional
Source Centre de Recherche de l'Institut Universitaire de Geriatrie de Montreal
Contact
Status Completed
Phase N/A
Start date May 2013
Completion date July 2017

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