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NCT01479816 Clinical Trial

Urinary Continence Index for Prediction of Urinary Incontinence in Older Women

Urinary Incontinence Clinical Trial

Official title:
Urinary Continence Index for Prediction of Urinary Incontinence in Older Women

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01479816
Other study ID # E2011-047
Secondary ID 1R01AG038673
Status Completed
Phase N/A
First received November 22, 2011
Last updated July 19, 2016
Start date September 2011
Est. completion date December 2015

Study information
Verified date July 2016
Source William Beaumont Hospitals
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

This study will analyse existing data to establish a clinically useful index to predict those women who are more likely to become incontinent. This would create significant opportunities for focused prevention and early intervention strategies.

Recruitment information / eligibility
Status Completed
Enrollment 702
Est. completion date December 2015
Est. primary completion date September 2015
Accepts healthy volunteers No
Gender Female
Age group 55 Years and older
Eligibility Inclusion Criteria:

- Women

Exclusion Criteria:

- Men

Study Design

Observational Model: Ecologic or Community, Time Perspective: Retrospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States Oakland University Rochester Michigan
United States William Beaumont Hospital Royal Oak Michigan

Sponsors (2)
Lead Sponsor Collaborator
Ananias Diokno National Institute on Aging (NIA)

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Index Estimation for Urinary Incontinence Prediction Several risk factors identified can serve as an index in predicting the development of urinary incontinence in elderly women. 2 years No
Secondary Predictive Reliability of Urinary Incontinence Index and its Validation The urinary continence index developed in Outcome measure 1 will reliably predict the development of urinary incontinence in women when tested against existing datasets. 3 years No
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