[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100527877":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":18,"centralContacts":18,"locations":18,"responsibleParty":25,"collaborators":30,"id":34,"slug":35,"hasResults":36,"nctId":37,"briefTitle":38,"officialTitle":38,"acronym":18,"eligibilityCriteria":39,"healthyVolunteers":36,"sex":40,"minAge":41,"maxAge":42,"enrollmentInfo":43,"targetDuration":18,"studyType":46,"phases":47,"briefSummary":49,"conditions":50,"keywords":54,"overallStatus":60,"whyStopped":18,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":18},{"fullName":5,"class":6},"Chinese University of Hong Kong","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"VR-based sensory stimulation","EXPERIMENTAL","Participants in the experimental group will receive VR-based sensory stimulation.",[13],"Device: VR-based intervention",{"label":15,"type":16,"description":17,"interventionNames":18},"Usual care","NO_INTERVENTION","Participants in the control group will receive usual care.",null,[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":18},"DEVICE","VR-based intervention","The Virtual Reality-based sensory stimulation intervention will last for up to fourteen days, with all interventions administered by a research team. The primary outcomes will include delirium incidence, duration, and severity. The secondary outcomes will encompass patients' psychological well-being (post-traumatic stress disorder, sleep quality, and ICU memory), patients' clinical outcomes, and other outcomes (quality of life, independence, and cognitive function).",[9],{"type":26,"investigatorFullName":27,"investigatorTitle":28,"investigatorAffiliation":29,"oldNameTitle":18,"oldOrganization":18},"PRINCIPAL_INVESTIGATOR","Liang Surui","Dr","Shenzhen Hospital of Southern Medical University",[31,32],{"name":29,"class":6},{"name":33,"class":6},"Peking University Shenzhen Hospital","100527877","effectiveness-of-a-virtual-reality-based-sensory-stimulation-intervention-in-preventing-delirium-in-intensive-care-units-100527877",false,"NCT06153472","Effectiveness of a Virtual Reality-Based Sensory Stimulation Intervention in Preventing Delirium in Intensive Care Units","Inclusion Criteria:\n\n* All ICU patients admitted to the study setting will be recruited if they are have: (1) ≥ 18 years, (2) the first time admitted to ICU and (3) a Richmond Agitation-Sedation Scale (RASS) score ≥-3\n\nExclusion Criteria:\n\n* Patients will be excluded if they have: (1) been diagnosed with dementia, delirium or acute psychiatric illness at admission, (2) been diagnosed with end-stage cancer, (3) severe hearing impairment and cannot be corrected by hearing aids and (4) been admitted to ICU with radioactive material.","ALL","18 Years","90 Years",{"count":44,"type":45},324,"ESTIMATED","INTERVENTIONAL",[48],"NA","The goal of this clinical trial is to evaluate the effectiveness of a VR-based sensory stimulation system in preventing ICU delirium in patients. The main questions it aims to answer are:\n\nIs the VR-based sensory stimulation system more effective in preventing ICU delirium compared to usual care? Does VR sensory stimulation improve patient psychological well-being and clinical outcomes in the ICU?\n\nParticipants will:\n\nExperimental Group:\n\nEngage in VR-based sensory stimulation sessions involving visual or\u002Fand auditory stimulation.\n\nControl Group:\n\nReceive usual care without additional VR-based interventions.\n\nComparison:\n\nResearchers will compare the outcomes between the experimental group (receiving VR-based sensory stimulation) and the control group (receiving usual care) to determine the effects of VR sensory stimulation on ICU delirium prevention, as well as its impact on patient psychological well-being and clinical outcomes.",[51,52,53],"Delirium","Intensive Care Unit","Randomised Controlled Trial",[55,56,57,58,59],"delirium","intensive care unit","randomised controlled trial","sensory stimulation","virtual reality","NOT_YET_RECRUITING","2023-11-22",{"date":63,"type":64},"2023-12-01","ACTUAL",{"date":66,"type":45},"2024-01",{"date":68,"type":45},"2026-12",{"name":5,"class":6}]