[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100561160":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":24,"centralContacts":29,"locations":36,"responsibleParty":62,"collaborators":65,"id":69,"slug":70,"hasResults":71,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":75,"eligibilityCriteria":76,"healthyVolunteers":71,"sex":77,"minAge":78,"maxAge":12,"enrollmentInfo":79,"targetDuration":12,"studyType":82,"phases":83,"briefSummary":85,"conditions":86,"keywords":94,"overallStatus":39,"whyStopped":12,"lastUpdateSubmitDate":103,"lastUpdatePostDateStruct":104,"startDateStruct":107,"completionDateStruct":109,"leadSponsor":111,"locationsCount":112},{"fullName":5,"class":6},"Lady Davis Institute","OTHER",[8,13],{"label":9,"type":10,"description":11,"interventionNames":12},"Phase 1 (Control group)","NO_INTERVENTION","Participants will be able to engage in care as per current family engagement practices. Family members in the usual care group will not participate in daily ICU rounds. In-person or virtual family participation in rounds is not routinely performed at any of the trial sites.",null,{"label":14,"type":15,"description":16,"interventionNames":17},"Phase 2 (Intervention)","EXPERIMENTAL","Participants in the Intervention group will be invited to participate in attending team rounds.",[18],"Other: Participation in attending team rounds",[20],{"type":6,"name":21,"description":22,"armGroupLabels":23,"otherNames":12},"Participation in attending team rounds","Family members can participate both in-person and virtually, which can vary daily if desired. If the family member wishes to participate in-person, they will be invited to be present when the team rounds in the ICU. If the family member wishes to participate virtually, they will be provided with a personalized link by email to attend rounds.",[14],[25],{"name":26,"affiliation":27,"role":28},"Michael J Goldfarb, MD, MSc","Lady Davis Institute, McGill University, Jewish General Hospital","PRINCIPAL_INVESTIGATOR",[30],{"name":31,"role":32,"phone":33,"phoneExt":34,"email":35},"Jillian Kifell, MSc","CONTACT","5143408222","25806","jillian.kifell.ccomtl@ssss.gouv.qc.ca",[37,53],{"facility":38,"status":39,"city":40,"state":41,"zip":12,"country":42,"countryCode":43,"cosmosGeoPoint":44,"geoPoint":49,"contacts":50},"Jewish General Hospital","RECRUITING","Montreal","Quebec","Canada","CA",{"type":45,"coordinates":46},"Point",[47,48],-73.58781,45.50884,{"lat":48,"lon":47},[51,52],{"name":31,"role":32,"phone":33,"phoneExt":34,"email":35},{"name":26,"role":28,"phone":12,"phoneExt":12,"email":12},{"facility":54,"status":55,"city":40,"state":41,"zip":12,"country":42,"countryCode":43,"cosmosGeoPoint":56,"geoPoint":58,"contacts":59},"McGill University Health Centre","NOT_YET_RECRUITING",{"type":45,"coordinates":57},[47,48],{"lat":48,"lon":47},[60,61],{"name":31,"role":32,"phone":33,"phoneExt":34,"email":35},{"name":26,"role":28,"phone":12,"phoneExt":12,"email":12},{"type":28,"investigatorFullName":63,"investigatorTitle":64,"investigatorAffiliation":5,"oldNameTitle":12,"oldOrganization":12},"Michael Goldfarb","Attending Staff, Division of Cardiology",[66],{"name":67,"class":68},"Canadian Institutes of Health Research (CIHR)","OTHER_GOV","100561160","the-family-icu-trial-100561160",false,"NCT06586541","The Family-ICU Trial","Family Participation in Intensive Care Unit Rounds (The Family-ICU Trial)","Family-ICU","Inclusion Criteria:\n\n* Adult family members (age ≥ 18 years) of ICU patients\n* Expected ICU stay ≥ 48 hours\n* Family members wishing to participate in rounds virtually must have the technological capability and understanding to participate virtually (must have a phone or computer with internet and audio\u002Fvideo capabilities)\n\nExclusion Criteria:\n\n* Family members who do not wish to participate in care\n* Repeat admissions within the study period\n* Another family member has already participated in the study","ALL","18 Years",{"count":80,"type":81},194,"ESTIMATED","INTERVENTIONAL",[84],"NA","Family inclusion in adult intensive care unit (ICU) rounds is recommended by critical care professional societies, yet widespread uptake of this practice is limited. A key barrier cited by ICU clinicians is insufficient evidence to support this practice. There is a need for robust evidence to support family participation in adult ICU rounds and influence change to routine clinical care. The primary purpose of this study is to assess whether family participation in adult ICU rounds improves family engagement in care. The secondary objectives are to assess family satisfaction, and anxiety and depression, to explore user experiences of family participation in ICU rounds, and to evaluate strategies to improve family member recruitment and retention rates. This is a stepped-wedge cluster randomized trial (n=194) at 6 Canadian ICUs. The stepped wedge cluster randomized trial is a pragmatic study design that overcomes methodological limitations in evaluating a healthcare service delivery intervention. In the stepped-wedge cluster design, there is random and sequential crossover of clusters from control (phase 1) to intervention (phase 2) until all clusters are exposed. The stepped-wedge design also allows each site to function as its own control. The stepped-wedge design is more powerful than a parallel design when substantial cluster level effects are present.",[87,88,89,90,91,92,93],"Virtual Care","Family Engagement","Patient and Family Engagement","Health Care Delivery","Family-centered Care","Physician Rounds","Critical Care, Intensive Care",[95,96,88,97,98,99,100,101,102,92],"Patient- and Family-Centered","Patient- and Family-Centered Care","Critical Care","Intensive Care Unit","Person-Centered Care","Delivery of Health Care","Virtual Rounds","Family Participation in Rounds","2026-03-25",{"date":105,"type":106},"2026-03-31","ACTUAL",{"date":108,"type":106},"2024-11-18",{"date":110,"type":81},"2029-07",{"name":5,"class":6},2]