Status:
COMPLETED
Mindfulness-Based Stress Reduction Techniques and Yoga for Treatment of Urinary Urge Incontinence (MBSR-Yoga)
Lead Sponsor:
University of Utah
Conditions:
Urinary Incontinence
Urinary Incontinence, Urge
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
Many women experience the accidental loss of urine called urge incontinence or overactive bladder (OAB) incontinence. Women describe this as a sudden, strong desire to pass urine which results in leak...
Eligibility Criteria
Inclusion
- Females at least 18 years of age
- Five or more urge urinary incontinence episodes on a three-day voiding diary. Urge incontinence episodes will be determined based on voiding diary and subject indication of coincident urge symptoms, allowing self-characterization of incontinence type.
- Urge predominant (urge \>50% of total incontinent episodes) urinary incontinence based on self-reported characterization of incontinent episodes on diary.
- Request for treatment for urge urinary incontinence.
- Subject is able to complete all study related items and interviews.
Exclusion
- Any current or recent (past 4 weeks) anticholinergic medication use. Patient may discontinue medication and after 4 weeks may be eligible for study.
- Past non-pharmacologic treatment for urge incontinence such as supervised behavioral therapy, supervised or unsupervised physical therapy, supervised biofeedback, and transvaginal electrical stimulation.
- Current symptomatic urinary tract infection that has not resolved prior start of MBSR group.
- Symptoms of pelvic organ prolapse screened by PFDI (Pelvic Floor Disorder Inventory question #3) "Do you have a bulge or something falling out that you can see or feel in the vaginal area?"
- Previous or currently implanted neuromodulation (sacral or tibial).
- Surgically altered detrusor muscle, such as augmentation cystoplasty.
- Women with known neurologic disease believed to potentially affect urinary function (Multiple sclerosis, spinal cord injuries, myasthenia gravis, Charcot-Marie-Tooth disease).
- In the opinion of the investigator, inability to understand diary instructions and complete 3-day voiding diary.
- Subject has been previously diagnosed with interstitial cystitis or chronic pelvic pain syndrome.
- Currently pregnant or within 6 months postpartum (pregnancy is not excluded for safety reasons but for quality of data)
Key Trial Info
Start Date :
February 1 2011
Trial Type :
INTERVENTIONAL
End Date :
February 1 2013
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT01470560
Start Date
February 1 2011
End Date
February 1 2013
Last Update
December 11 2014
Active Locations (1)
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1
University of Utah
Salt Lake City, Utah, United States, 84112