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IRIS: Incontinence Research Intervention Study

Primary Purpose

Urinary Incontinence, Urinary Incontinence, Stress

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Knack therapy
Sponsored by
University of Michigan
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Urinary Incontinence focused on measuring pelvic muscle therapy, urinary incontinence therapy, stress incontinence intervention, incontinence intervention, Incontinence, SUI, Stress Incontinence

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Women who are incontinent Women who experience leakage with coughing, sneezing or exercising Women who are generally healthy Women who are over the age of eighteen Women who are not pregnant nor expecting to become pregnant within a year Exclusion Criteria: No urine leakage when coughing, sneezing, or exercising Under the age of eighteen Pregnant or expecting to become pregnant Untreated urinary tract infection Pronounced pain or discomfort with pelvic exams History of neurologic conditions

Sites / Locations

  • University of Michigan, School of Nursing

Outcomes

Primary Outcome Measures

The short-term outcome of "positive response" is defined as able to reduce leakage during coughing to under 2 ml or 50% decrease from baseline (whichever is more stringent). This will be evaluated immediately at 1 month.

Secondary Outcome Measures

Long-term success (3-months and 1-year) is defined both by the paper towel test criteria and by documentation of at least 50% reduction of leakage in diary to reflect success at home.

Full Information

First Posted
July 27, 2005
Last Updated
November 9, 2010
Sponsor
University of Michigan
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
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1. Study Identification

Unique Protocol Identification Number
NCT00125177
Brief Title
IRIS: Incontinence Research Intervention Study
Official Title
Office for Research on Women's Health (ORWH): Specialized Centers of Research (SCOR) on Sex and Gender Factors Affecting Women's Health. Project 3: Selection Criteria For Muscle Therapy in SUI
Study Type
Interventional

2. Study Status

Record Verification Date
July 2005
Overall Recruitment Status
Completed
Study Start Date
January 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
April 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University of Michigan
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

4. Oversight

5. Study Description

Brief Summary
The IRIS project stands for Incontinence Research Intervention Study. The purpose of this research project is to develop an effective behavioral therapy for urinary incontinence and specifically to test Knack therapy, a self-help treatment. The Knack therapy involves learning the skill of performing a pelvic muscle contraction simultaneously with an event known to trigger leakage, in order to stop that leakage.
Detailed Description
This proposal aims to develop and test, in a general population of women with stress urinary incontinence (SUI), a model for predicting who will succeed in overcoming incontinence long-term (1-year) by simply using Knack therapy (thus avoiding invasive and costly surgery and time consuming Kegel's exercises). Specific Aims are to: develop a logistic regression model to predict success with the Knack; validate the model by determining the proportion of people who succeed according to who is predicted to succeed; and develop long-term effectiveness of the Knack (1-year). The project will be implemented in three phases: model development (n=160 women), model validation (n~160), and long-term follow-up of women who demonstrate response. This will be evaluated immediately and at 1 month and at 3-months and 1-year.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Incontinence, Urinary Incontinence, Stress
Keywords
pelvic muscle therapy, urinary incontinence therapy, stress incontinence intervention, incontinence intervention, Incontinence, SUI, Stress Incontinence

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
320 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Behavioral
Intervention Name(s)
Knack therapy
Primary Outcome Measure Information:
Title
The short-term outcome of "positive response" is defined as able to reduce leakage during coughing to under 2 ml or 50% decrease from baseline (whichever is more stringent). This will be evaluated immediately at 1 month.
Secondary Outcome Measure Information:
Title
Long-term success (3-months and 1-year) is defined both by the paper towel test criteria and by documentation of at least 50% reduction of leakage in diary to reflect success at home.

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women who are incontinent Women who experience leakage with coughing, sneezing or exercising Women who are generally healthy Women who are over the age of eighteen Women who are not pregnant nor expecting to become pregnant within a year Exclusion Criteria: No urine leakage when coughing, sneezing, or exercising Under the age of eighteen Pregnant or expecting to become pregnant Untreated urinary tract infection Pronounced pain or discomfort with pelvic exams History of neurologic conditions
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Janis M Miller, PhD, APRN
Organizational Affiliation
University of Michigan, School of Nursing, Dept. Obstetrics & Gynecology
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
John OL DeLancey, MD
Organizational Affiliation
University of Michigan, Obstetrics & Gynecology
Official's Role
Study Director
Facility Information:
Facility Name
University of Michigan, School of Nursing
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States

12. IPD Sharing Statement

Learn more about this trial

IRIS: Incontinence Research Intervention Study

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