[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"physician-rounds\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:physician-rounds":32},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,55],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":34,"overallStatus":43,"whyStopped":4,"lastUpdateSubmitDate":44,"lastUpdatePostDateStruct":45,"startDateStruct":48,"completionDateStruct":50,"leadSponsor":52,"locationsCount":5},"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":20,"type":21},194,"ESTIMATED","INTERVENTIONAL",[24],"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.",[27,28,29,30,31,32,33],"Virtual Care","Family Engagement","Patient and Family Engagement","Health Care Delivery","Family-centered Care","Physician Rounds","Critical Care, Intensive Care",[35,36,28,37,38,39,40,41,42,32],"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","RECRUITING","2026-03-25",{"date":46,"type":47},"2026-03-31","ACTUAL",{"date":49,"type":47},"2024-11-18",{"date":51,"type":21},"2029-07",{"name":53,"class":54},"Lady Davis Institute","OTHER",{"id":56,"slug":57,"hasResults":11,"nctId":58,"briefTitle":59,"officialTitle":60,"acronym":4,"eligibilityCriteria":61,"healthyVolunteers":11,"sex":62,"minAge":18,"maxAge":4,"enrollmentInfo":63,"targetDuration":4,"studyType":22,"phases":65,"briefSummary":66,"conditions":67,"keywords":4,"overallStatus":43,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":5},"100609509","timing-of-physician-rounds-for-antepartum-patients-100609509","NCT07215507","Timing of Physician Rounds for Antepartum Patients","Effect of Timing of Physician Rounds on Hospital Experience for High-Risk Antepartum Patients: A Randomized Controlled TrialTiming of Physician Rounds for Antepartum Patients","Inclusion Criteria:\n\n* Pregnant women greater than 20 weeks gestation admitted to the antepartum list at Duke University Hospital\n\nExclusion Criteria:\n\n* Stillbirth\n* ICU admission\n* Admission to off-service unit\n* Active magnesium sulfate administration\n* Active severe hypertension or initiation of anti-hypertensive pathway within past 8 hours\n* Category II fetal heart rate tracing\n* Other pregnancy\u002Fdelivery complication precluding delayed rounding\n* Unstable\u002Funsuitable condition per overnight team or attending physician\n* Previously enrolled\u002Fon active board \\>1 day at morning rounds\n* Postpartum readmission\n* Antepartum admission within the last 4 weeks","FEMALE",{"count":64,"type":21},200,[24],"This study will include patients admitted to the Antepartum service at Duke University Hospital, many of whom are managing high-risk pregnancies that require extended hospital stays and frequent physician interactions. Currently, two rounding methods are used interchangeably for patients who do not have pregnancy or delivery complications that would preclude participation in delayed daytime rounding. This randomized controlled trial will compare two rounding models: the standard model, in which patients receive two rounds (an early morning bedside encounter and a later team discussion), and the intervention model, which consolidates both rounds into a single, later-morning bedside encounter following the team's review of clinical data. The primary objective is to assess whether consolidating physician rounds into a single, later-morning encounter-referred to as discovery rounding-improves patient satisfaction with communication.",[32,68],"Communication","2026-01-28",{"date":71,"type":47},"2026-01-29",{"date":73,"type":47},"2025-11-04",{"date":75,"type":21},"2027-02-20",{"name":77,"class":54},"Duke University"]