[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100591846":3},{"organization":4,"armGroups":7,"interventions":17,"overallOfficials":11,"centralContacts":22,"locations":11,"responsibleParty":32,"collaborators":11,"id":34,"slug":35,"hasResults":36,"nctId":37,"briefTitle":38,"officialTitle":38,"acronym":39,"eligibilityCriteria":40,"healthyVolunteers":36,"sex":41,"minAge":42,"maxAge":11,"enrollmentInfo":43,"targetDuration":11,"studyType":46,"phases":47,"briefSummary":49,"conditions":50,"keywords":11,"overallStatus":51,"whyStopped":11,"lastUpdateSubmitDate":52,"lastUpdatePostDateStruct":53,"startDateStruct":56,"completionDateStruct":58,"leadSponsor":60,"locationsCount":11},{"fullName":5,"class":6},"Centre Médical Porte Verte","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"VR group","EXPERIMENTAL",null,[13],"Other: Virtual Reality",{"label":15,"type":16,"description":11,"interventionNames":11},"contrrol arm","NO_INTERVENTION",[18],{"type":6,"name":19,"description":20,"armGroupLabels":21,"otherNames":11},"Virtual Reality","Use of virtual reality to elicit positive emotions and improve the well-being of elderly patients hospitalized in SMR",[9],[23,29],{"name":24,"role":25,"phone":26,"phoneExt":27,"email":28},"Baptiste ISABET","CONTACT","0634227138","0033","Baptiste.ISABET@lpv.univi.fr",{"name":30,"role":25,"phone":11,"phoneExt":11,"email":31},"Fatima Zohra IZEDAREN","Fatima-Zohra.Izedaren@lpv.univi.fr",{"type":33,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100591846","contribution-of-virtual-reality-to-the-well-being-of-elderly-patients-hospitalized-in-smr-100591846",false,"NCT06985732","Contribution of Virtual Reality to the Well-being of Elderly Patients Hospitalized in SMR","RV-SMR","Inclusion Criteria:\n\nPeople hospitalized in the SMR unit at La Porte Verte Hospital for a minimum of 3 weeks,\n\n* People with preserved or slightly impaired cognitive status with an MMSE ≥ 20,\n* People who have been informed and have signed written informed consent\n\nExclusion Criteria:\n\nPeople under guardianship or curatorship,\n\n* People with difficulty understanding the VR study and materials,\n* People with vision problems that impact the use of VR,\n* People with hearing problems that impact the use of VR,\n* People with epilepsy,\n* People at risk of nausea and dizziness when using the VR headset,\n* People who cannot tolerate the VR headset,\n* Not affiliated with a social security scheme.\n* People receiving care with reflexology and relaxation massage","ALL","70 Years",{"count":44,"type":45},50,"ESTIMATED","INTERVENTIONAL",[48],"NA","The objective of this clinical trial is to evaluate the effect of using virtual reality on the well-being of elderly patients hospitalized in SMR for 3 weeks. The study also allows to evaluate the effect of VR on apathy, and the autonomy of patients hospitalized in the SMR department for 3 weeks.",[19],"NOT_YET_RECRUITING","2025-05-22",{"date":54,"type":55},"2025-05-28","ACTUAL",{"date":57,"type":45},"2025-09-01",{"date":59,"type":45},"2026-09-01",{"name":5,"class":6}]