University of Wisconsin-Madison School of Medicine and Public Health
Madison, Wisconsin, 53792, United States
NCT Number: NCT03140852
The goal of this study is to obtain data about the effectiveness, reach, adoption, and implementation potential of an innovative, combined urinary/bowel continence workshop through a randomized controlled trial in six Wisconsin communities. This three-session workshop is based on proven principles of behavior change addressing urinary and bowel continence self-management and health education and has been developed specifically for administration to women age 50 and older in senior centers. We hypothesize that workshop participants will experience improvements in urinary and bowel incontinence symptoms, will have increased levels of care-seeking and self-efficacy for these conditions, and will maintain the self-management strategies taught in the workshop 3 months following completion of the workshop. We further hypothesize that this workshop will reach its intended target population (independent senior women with incontinence) and will improve their mental health by destigmatizing the condition of incontinence.
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Notify Me50 year and older
Female
Interventional
Not applicable
Madison, Wisconsin, 53792, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
This three-session workshop is based on proven principles of behavior change addressing urinary and bowel continence self-management and health education and has been developed specifically for administration to women age 50 and older in senior centers.
Time frame: 3 months after treatment group completes intervention
Patient Global Impression of Improvement (PGI-I) regarding bladder or bowel incontinence
Time frame: 3 months after treatment group completes intervention
validated instrument
Time frame: 3 months after treatment group completes intervention
validated instrument
Time frame: 3 months after treatment group completes intervention
validated instrument
Time frame: 3 months after treatment group completes intervention
validated instrument
University of Wisconsin, Madison
Other
Acronym: SHAIP
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