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OpenTrials
Completed

NCT Number: NCT01479816

Urinary Continence Index for Prediction of Urinary Incontinence in Older Women

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.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women

Exclusion criteria

  • Men

Treatment and study plan

Primary outcomes

  1. 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 outcomes

  1. 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.

Sponsors and collaborators

Lead sponsor

Ananias Diokno

Other

Collaborators

  • National Institute on Aging (NIA)

Registry information

Important dates

Study start
2011
Primary completion
2015
Study completion
2015
First posted
Nov 24, 2011
Registry last updated
Jul 21, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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