[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"virtual-care\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:virtual-care":27},{"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":59,"acronym":4,"eligibilityCriteria":60,"healthyVolunteers":11,"sex":61,"minAge":18,"maxAge":4,"enrollmentInfo":62,"targetDuration":64,"studyType":65,"phases":4,"briefSummary":66,"conditions":67,"keywords":76,"overallStatus":43,"whyStopped":4,"lastUpdateSubmitDate":82,"lastUpdatePostDateStruct":83,"startDateStruct":85,"completionDateStruct":87,"leadSponsor":89,"locationsCount":91},"100583536","canada-wide-implementation-of-a-virtual-sexual-health-and-rehabilitation-eclinic-shareclinic-for-prostate-cancer-patients-and-their-partners-100583536","NCT06877598","Canada-wide Implementation of a Virtual Sexual Health and Rehabilitation eClinic (SHAReClinic) for Prostate Cancer Patients and Their Partners","Inclusion Criteria:\n\n* Patients who are scheduled for first-line treatment for localized prostate cancer, either through radical prostatectomy (open or robotic) or radiation treatment (brachytherapy, external beam) Alone, or with adjuvant Androgen Deprivation Therapy (ADT) OR\n\n  * Patients currently undergoing active treatment for prostate cancer OR\n  * Patients who have undergone cancer treatment in the past 6 months\n  * Patients who are hormone and\u002For chemotherapy-naïve\n  * Patients who have access to a computer or smartphone with internet access\n  * Patients who are 18 years of age or older\n\nExclusion Criteria:\n\n* Patients on ADT alone as primary treatment, and\u002For patients on chemotherapy\n* Patients who lack English proficiency\n* Patients on nitrate therapy or have other contra-indications to phosphodiesterase type 5 inhibitors (PDE5i's)\n* Patients with medical conditions that would preclude safe sexual activity\n* Patients who have had previous treatment for PCa","MALE",{"count":63,"type":21},575,"12 Months","OBSERVATIONAL","The goal of this observational study is to evaluate the effectiveness of SHAReClinic, a national, virtual Sexual Health and Rehabilitation eClinic designed to support prostate cancer patients and their partners. Specifically, this study aims to assess SHAReClinic's impact on improving sexual function, satisfaction, and relational intimacy after treatment.\n\nThe primary objective is to evaluate SHAReClinic's effectiveness across participating sites and determine its role in supporting long-term sexual health and well-being.\n\nAs part of usual care, newly enrolled SHAReClinic patients will receive guided education modules and access to sexual health counselling at key recovery milestones.\n\nSHAReClinic seeks to expand access to sexual health care for prostate cancer patients across Canada by providing evidence-based, virtual sexual rehabilitation. Findings from this study will inform best practices in survivorship care and contribute to the development of a national standard for oncology sexual health interventions.",[68,69,70,71,27,72,73,74,75],"Prostate Cancer","Sexual Dysfunction, Physiological","Sexual Dysfunction, Psychological","Sexual Dysfunction","Virtual Clinic","Survivorship","Implementation of Evidence Based Programs","Implementation",[71,77,78,75,79,80,81,73],"Prostate cancer","Virtual health","Consolidated Framework for Implementation Research (CFIR)","Bio-psychosocial","Reach Effectiveness Adoption Implementation and Maintenance (RE-AIM)","2025-12-09",{"date":84,"type":47},"2025-12-11",{"date":86,"type":47},"2025-06-01",{"date":88,"type":21},"2027-12",{"name":90,"class":54},"University Health Network, Toronto",10]