[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"virtual-clinic\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:virtual-clinic":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,53],{"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":32,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100588092","virtual-ward-for-early-discharge-in-patients-receiving-inpatient-care-100588092",false,"NCT06936891","Virtual Ward for Early Discharge in Patients Receiving Inpatient Care","Virtual Ward for Early Discharge in Patients Receiving Inpatient Care: A Prospective Feasibility Study on Home Monitoring for the Early Discharge of Eligible Hospitalized Patients in an Outpatient Setting","VIP care","Inclusion Criteria:\n\n* Adult patients (≥18 years old).\n* Currently hospitalized and eligible for early discharge according to clinical judgment.\n* Ability to provide written informed consent.\n* Access to a smartphone or tablet with internet connection.\n* Patient is capable of using the Digizorg app or has support from a caregiver who can assist.\n* Suitable home situation for Virtual Ward care (e.g., safe environment, necessary utilities available).\n* Enrollment in one of the predefined Virtual Ward care pathways\n\nExclusion Criteria:\n\n* Patients requiring continuous hospital-based monitoring or interventions that cannot be safely delivered at home.\n* Patients who are hemodynamically unstable or require oxygen therapy \\>5 liters\u002Fminute at the time of discharge.\n* Patients unable or unwilling to comply with home monitoring procedures.\n* Patients with significant cognitive impairment without adequate caregiver support.\n* Patients with a life expectancy less than 30 days, as assessed by the treating physician.\n* Patients participating in another interventional clinical trial that could interfere with the Virtual Ward protocol.\n* Any other condition that, in the opinion of the treating physician, would make participation unsafe or infeasible.","ALL","18 Years",{"count":20,"type":21},306,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study evaluates the feasibility of providing hospital-level care at home for eligible patients through a Virtual Ward. Patients are discharged early from the hospital and monitored remotely using digital vital sign monitoring and anamnesis questionnaires. The primary aim is to determine if at least 30% of eligible patients can be safely and successfully transferred to the Virtual Ward under current Dutch healthcare conditions.",[27,28,29,30,31],"Early Discharge","Telemedicine","Virtual Clinic","Hospital at Home","Feasibility Studies",[33,34,35,36,37,38,39],"early discharge","telemedicine","virtual ward","virtual clinic","hospital at home","feasability","telemonitoring","RECRUITING","2026-02-15",{"date":43,"type":44},"2026-02-17","ACTUAL",{"date":46,"type":44},"2025-04-16",{"date":48,"type":21},"2028-12-31",{"name":50,"class":51},"Erasmus Medical Center","OTHER",1,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":57,"acronym":4,"eligibilityCriteria":58,"healthyVolunteers":11,"sex":59,"minAge":18,"maxAge":4,"enrollmentInfo":60,"targetDuration":62,"studyType":63,"phases":4,"briefSummary":64,"conditions":65,"keywords":74,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":89},"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":61,"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.",[66,67,68,69,70,29,71,72,73],"Prostate Cancer","Sexual Dysfunction, Physiological","Sexual Dysfunction, Psychological","Sexual Dysfunction","Virtual Care","Survivorship","Implementation of Evidence Based Programs","Implementation",[69,75,76,73,77,78,79,71],"Prostate cancer","Virtual health","Consolidated Framework for Implementation Research (CFIR)","Bio-psychosocial","Reach Effectiveness Adoption Implementation and Maintenance (RE-AIM)","2025-12-09",{"date":82,"type":44},"2025-12-11",{"date":84,"type":44},"2025-06-01",{"date":86,"type":21},"2027-12",{"name":88,"class":51},"University Health Network, Toronto",10]