Further Enhancing Non-pharmacologic Therapy for Incontinence
Urge Urinary Incontinence
About this trial
This is an interventional treatment trial for Urge Urinary Incontinence focused on measuring urge incontinence, biofeedback, pelvic floor muscle training, behavior modification
Eligibility Criteria
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.
Sites / Locations
- Geriatric Continence Research Unit, NE547 Montefiore UPMC
Arms of the Study
Arm 1
Experimental
Biofeedback
Biofeedback assisted pelvic floor muscle therapy (3 visits)