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A Well-Being Intervention for People With IBS

StatusNot Yet Recruiting
PhaseNot applicable
Started
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Record History

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  1. Start date pushed from Sep 2026 to Dec 2026
    • Eligibility criteria expanded, about 9 words
    • Study description revised
  2. Re-verified, no change to tracked fieldsv4
  3. Start date: Aug 2026 to Sep 2026v3
  4. Study description expanded, about 3 wordsv2
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT07600047
Lead Sponsor University of Wisconsin, Madison
Conditions
(from sponsor)		 Irritable Bowel Syndrome
Related terms Irritable Bowel Syndrome
Enrollment 150 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov