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OpenTrials
Completed

NCT Number: NCT03140852

Community-Based Continence Promotion: Sustaining Healthy Aging in Place (SHAIP) Through Mind Over Matter (MOM)

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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Key information

Age range

50 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

University of Wisconsin-Madison School of Medicine and Public Health

Madison, Wisconsin, 53792, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • qualifying symptoms within last 3 months
  • able to speak English
  • lives independently

Exclusion criteria

  • new treatment for target symptoms within last 3 months

Treatment and study plan

Mind Over Matter; Healthy Bowels, Healthy Bladder

Behavioral

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.

Primary outcomes

  1. Symptom Improvement

    Time frame: 3 months after treatment group completes intervention

    Patient Global Impression of Improvement (PGI-I) regarding bladder or bowel incontinence

Secondary outcomes

  1. Pelvic Floor Distress Inventory-20

    Time frame: 3 months after treatment group completes intervention

    validated instrument

  2. Geriatric Self-Efficacy for Urinary Incontinence (GSE-UI)

    Time frame: 3 months after treatment group completes intervention

    validated instrument

  3. Barriers to Care-seeking for Accidental Bowel Leakage (BCABL)

    Time frame: 3 months after treatment group completes intervention

    validated instrument

  4. Barriers to Incontinence Care-seeking (BICS-Q)

    Time frame: 3 months after treatment group completes intervention

    validated instrument

Sponsors and collaborators

Lead sponsor

University of Wisconsin, Madison

Other

Collaborators

  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
  • Wisconsin Partnership Program

Registry information

Acronym: SHAIP

Important dates

Study start
2017
Primary completion
2017
Study completion
2017
First posted
May 4, 2017
Registry last updated
Aug 22, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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