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Urinary Continence Index for Prediction of Urinary Incontinence in Older Women

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01479816
First Posted: November 24, 2011
Last Update Posted: July 21, 2016
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
National Institute on Aging (NIA)
Information provided by (Responsible Party):
Ananias Diokno, William Beaumont Hospitals
  Purpose
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.

Condition
Urinary Incontinence

Study Type: Observational
Study Design: Observational Model: Ecologic or Community
Time Perspective: Retrospective
Official Title: Urinary Continence Index for Prediction of Urinary Incontinence in Older Women

Resource links provided by NLM:


Further study details as provided by Ananias Diokno, William Beaumont Hospitals:

Primary Outcome Measures:
  • Index Estimation for Urinary Incontinence Prediction [ Time Frame: 2 years ]
    Several risk factors identified can serve as an index in predicting the development of urinary incontinence in elderly women.


Secondary Outcome Measures:
  • Predictive Reliability of Urinary Incontinence Index and its Validation [ Time Frame: 3 years ]
    The urinary continence index developed in Outcome measure 1 will reliably predict the development of urinary incontinence in women when tested against existing datasets.


Enrollment: 702
Study Start Date: September 2011
Study Completion Date: December 2015
Primary Completion Date: September 2015 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   55 Years and older   (Adult, Senior)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Women 55 years and older
Criteria

Inclusion Criteria:

  • Women

Exclusion Criteria:

  • Men
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01479816


Locations
United States, Michigan
Oakland University
Rochester, Michigan, United States, 48309
William Beaumont Hospital
Royal Oak, Michigan, United States, 48073
Sponsors and Collaborators
Ananias Diokno
National Institute on Aging (NIA)
Investigators
Principal Investigator: Ananias Diokno, MD William Beaumont Hospitals
  More Information

Responsible Party: Ananias Diokno, Principal Investigator, William Beaumont Hospitals
ClinicalTrials.gov Identifier: NCT01479816     History of Changes
Other Study ID Numbers: E2011-047
1R01AG038673 ( U.S. NIH Grant/Contract )
First Submitted: November 22, 2011
First Posted: November 24, 2011
Last Update Posted: July 21, 2016
Last Verified: July 2016
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Keywords provided by Ananias Diokno, William Beaumont Hospitals:
continence
index

Additional relevant MeSH terms:
Urinary Incontinence
Enuresis
Urination Disorders
Urologic Diseases
Lower Urinary Tract Symptoms
Urological Manifestations
Signs and Symptoms
Behavioral Symptoms
Elimination Disorders
Mental Disorders