[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100638973":3},{"organization":4,"armGroups":7,"interventions":18,"overallOfficials":23,"centralContacts":28,"locations":33,"responsibleParty":46,"collaborators":11,"id":48,"slug":11,"hasResults":49,"nctId":50,"briefTitle":51,"officialTitle":51,"acronym":11,"eligibilityCriteria":52,"healthyVolunteers":49,"sex":53,"minAge":54,"maxAge":11,"enrollmentInfo":55,"targetDuration":11,"studyType":58,"phases":59,"briefSummary":61,"conditions":62,"keywords":64,"overallStatus":66,"whyStopped":11,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":76},{"fullName":5,"class":6},"University of Wisconsin, Madison","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Well-Being Intervention","EXPERIMENTAL",null,[13],"Behavioral: Well-Being Intervention",{"label":15,"type":16,"description":11,"interventionNames":17},"Waitlist Control (delayed Well-Being Intervention)","ACTIVE_COMPARATOR",[13],[19],{"type":20,"name":9,"description":21,"armGroupLabels":22,"otherNames":11},"BEHAVIORAL","The intervention will be once weekly over a 15-week period, lasting approximately one hour per session.",[15,9],[24],{"name":25,"affiliation":26,"role":27},"Mark Benson, MD","UW School of Medicine and Public Health","PRINCIPAL_INVESTIGATOR",[29],{"name":25,"role":30,"phone":31,"phoneExt":11,"email":32},"CONTACT","608-263-1995","mb4@medicine.wisc.edu",[34],{"facility":35,"status":11,"city":36,"state":37,"zip":38,"country":39,"cosmosGeoPoint":40,"geoPoint":45,"contacts":11},"UW Health Digestive Health Center","Madison","Wisconsin","53705","United States",{"type":41,"coordinates":42},"Point",[43,44],-89.40123,43.07305,{"lat":44,"lon":43},{"type":47,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100638973",false,"NCT07600047","A Well-Being Intervention for People With IBS","Inclusion Criteria:\n\n* Men and women currently diagnosed with Irritable Bowel Syndrome (IBS) by a healthcare provider.\n* Able to read and write in English.\n* Willing to complete questionnaires and participate in either the intervention or control group.\n* Capable of providing informed consent.\n* Must be a UW Health patient or referred through UW Digestive Health Center.\n\nExclusion Criteria:\n\n* Individuals with cognitive impairments or reading difficulties that would interfere with understanding study materials or completing assessments.\n* Individuals unable to provide informed consent.\n* Prior participation in a similar intervention study.\n* Non-English speakers (since study materials are in English)","ALL","18 Years",{"count":56,"type":57},150,"ESTIMATED","INTERVENTIONAL",[60],"NA","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.",[63],"Irritable Bowel Syndrome",[65],"well being","NOT_YET_RECRUITING","2026-05-19",{"date":69,"type":70},"2026-05-22","ACTUAL",{"date":72,"type":57},"2026-08",{"date":74,"type":57},"2027-08",{"name":5,"class":6},1]