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A Well-Being Intervention for People With IBS
Sponsor: University of Wisconsin, Madison
Summary
The purpose of this randomized behavioral clinical trial is to examine whether a well-being intervention can improve both psychological well-being and physical outcomes in adults with Irritable Bowel Syndrome (IBS). The study aims to assess whether this intervention decreases anger, anxiety, and depression; increases self-esteem, empathy, and hope; and improves quality of life indicators such as IBS symptom severity, sleep quality, fatigue, and diet. Participants can expect to be on study for up to 9 months.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
150
Start Date
2026-08
Completion Date
2027-08
Last Updated
2026-05-22
Healthy Volunteers
No
Conditions
Interventions
Well-Being Intervention
The intervention will be once weekly over a 15-week period, lasting approximately one hour per session.
Locations (1)
UW Health Digestive Health Center
Madison, Wisconsin, United States