Further Enhancing Non-pharmacologic Therapy for Incontinence



Status:Active, not recruiting
Conditions:Urology
Therapuetic Areas:Nephrology / Urology
Healthy:No
Age Range:60 - Any
Updated:4/21/2016
Start Date:February 2004
End Date:September 2016

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To determine the mechanisms mediating the therapeutic efficacy of pelvic floor muscle
exercises and biofeedback for urge urinary incontinence, as well as the characteristics of
patients most likely to respond. By identifying the key components of this treatment, we
hope to simplify it and make it more easily applicable, more effective, less expensive, and
thus more useful for people with urge incontinence in the future.

Urinary incontinence (UI) is prevalent and morbid in the elderly, and its associated costs
exceed $26 billion annually. Although effective therapy exists, it is underutilized. This is
particularly true for non-pharmacologic therapies, which are at least as effective as drugs
but safer, and recommended as the initial approach by every national panel. If therapies
such as biofeedback (which targets pelvic muscles and detrusor suppression) are to become
more widely used, they will require simplification, fewer and briefer sessions, less
expensive equipment, and less sophisticated therapists. Unfortunately, such protocols cannot
yet be devised because it is unknown which components are essential. We postulate that the
mechanisms mediating effectiveness can be identified and that such knowledge will make it
possible to enhance efficacy and to formulate more feasible and cost-effective protocols.
Since reduction in UI correlates weakly with improved quality of life, however, it is
important that biofeedback's impact on life quality be assessed concomitantly to ensure that
formulation of such streamlined methods does not eliminate components essential for improved
quality of life, even if they have no physiological correlates. We will address these issues
by treating at least 150 elderly subjects with urge UI in an 8-week course of biofeedback.
We will collect clinical and quality of life data and perform extensive physiologic testing
on each subject at baseline and 8 weeks later. Improvement will be correlated with change in
physiologic and quality of life parameters to identify the parameters that likely mediated
it. Knowledge from this study should identify predictors and mechanisms mediating success of
biofeedback; suggest ways that it could be further improved; facilitate development of less
expensive, quicker, and more feasible protocols to deliver it (potentially permitting
application to less motivated or cognitively impaired patients); and shed insight into
mechanisms that may even improve efficacy of other interventions.

Inclusion Criteria:

- ambulatory women over age 60, who are incontinent at least twice weekly for 3 months
despite correction of potentially reversible causes.

- urinary incontinence (urge or predominantly urge) by clinical criteria.

- able to accurately complete a voiding diary, to perform a 24-hour pad test under
direction, and to undergo instruction in biofeedback.

Exclusion Criteria:

- significant mental impairment [mini mental status exam (MMSE) ≤ 20)

- urethral obstruction

- history of bladder cancer

- spinal cord lesions

- multiple sclerosis

- pelvic radiation

- interstitial cystitis

- artificial sphincter implant

- expected to have changes in medications/doses during the trial

- medically unstable

- Patients with factors that could cause transient UI [e.g., current urinary tract
infection (UTI), acute confusion] will be treated in concert with the subject's
primary care provider and considered for enrollment if their UI persists.

- conditions that require endocarditis prophylaxis (such as heart valve problems or
bacterial endocarditis)

- being unable to undergo fMRI because of claustrophobia or any metallic objects in the
body, such pacemakers, metallic prostheses, aneurism clips or others.
We found this trial at
1
site
165
mi
from 43215
Pittsburgh, PA
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