A Well-Being Intervention for People With IBS

Part of paid clinical trials in Madison, Wisconsin.

Sponsor
University of Wisconsin, Madison
Study ID
NCT07600047
Status
Not Yet Recruiting

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Conditions

  • Irritable Bowel Syndrome

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Well-Being Intervention — BEHAVIORAL
    The intervention will be once weekly over a 15-week period, lasting approximately one hour per session.

Study Details

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 Dates

Start date
Aug 31, 2026
Status verified
May 2026
Primary completion
Aug 31, 2027
Completion
Aug 31, 2027

Study Design

Enrollment
150 participants (estimated)
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT

Arms

  • Experimental: Well-Being Intervention
  • Active Comparator: Waitlist Control (delayed Well-Being Intervention)

Primary Outcome Measure

Anger measured by PROMIS Anger Scale Score [ Time Frame: data collected up to 17 weeks with a 4 week follow up at 21 weeks on study for the first intervention and waitlist-control, data collected up to 34 weeks with a 4 week follow up at 38 weeks on study to complete data collection in the crossover group ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
UW Health Digestive Health CenterMadisonWisconsin53705-

Find similar trials in Madison, WI

By research site
UW Health Digestive Health Center· Madison, WI

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