[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100638973":3},{"organization":4,"armGroups":7,"interventions":18,"overallOfficials":23,"centralContacts":28,"locations":33,"responsibleParty":47,"collaborators":11,"id":49,"slug":50,"hasResults":51,"nctId":52,"briefTitle":53,"officialTitle":53,"acronym":11,"eligibilityCriteria":54,"healthyVolunteers":51,"sex":55,"minAge":56,"maxAge":11,"enrollmentInfo":57,"targetDuration":11,"studyType":60,"phases":61,"briefSummary":63,"conditions":64,"keywords":66,"overallStatus":68,"whyStopped":11,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":78},{"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,"countryCode":40,"cosmosGeoPoint":41,"geoPoint":46,"contacts":11},"UW Health Digestive Health Center","Madison","Wisconsin","53705","United States","US",{"type":42,"coordinates":43},"Point",[44,45],-89.40123,43.07305,{"lat":45,"lon":44},{"type":48,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100638973","a-well-being-intervention-for-people-with-ibs-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":58,"type":59},150,"ESTIMATED","INTERVENTIONAL",[62],"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.",[65],"Irritable Bowel Syndrome",[67],"well being","NOT_YET_RECRUITING","2026-05-19",{"date":71,"type":72},"2026-05-22","ACTUAL",{"date":74,"type":59},"2026-08",{"date":76,"type":59},"2027-08",{"name":5,"class":6},1]