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Group Learning Achieves Decreased Incidents of Lower Urinary Symptoms — Gladiolus  

Urinary Incontinence, Stress Clinical Trial

Official title:
Group Learning Achieves Decreased Incidents of Lower Urinary Symptoms

Clinical Trial Summary

This three-site randomized controlled trial compares the effectiveness and cost-effectiveness of a group-administered behavioral treatment program to no treatment. Women with stress, urgency, or mixed urinary incontinence will be recruited and screened centrally, evaluated clinically at each of three study sites, and random assigned to one of two treatment arms: 1. Group behavioral treatment or 2. No treatment. Group treatment modalities have the potential to reach a larger population of older women with urinary incontinence, not only in the traditional medical settings, but also in community settings. The investigators hypothesize that group behavioral treatment will be more effective than no treatment. The investigators hypothesize that the group treatment will be cost-effective compared to no treatment.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02001714
Study type Interventional
Source William Beaumont Hospitals
Contact
Status Completed
Phase N/A
Start date September 2013
Completion date December 2016
View Details
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