[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Centre Médical Porte Verte\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":78},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,39,60],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":4},"100626023",false,"NCT07430241","Impact of Implementing the Personalized Non-Pharmacological Therapies Method in Facilities for the Elderly","Impact of Implementing the Personalized Non-Pharmacological Therapies Method in Facilities for the Elderly - A Multicenter Comparative Study","IMPACT-TNmP","Inclusion Criteria:\n\n* Individuals aged 65 years and older;\n* Dependent older adults residing in institutional settings, including individuals under legal guardianship or trusteeship, who have been recently admitted to the facility;\n* Individuals presenting a neurocognitive disorder associated with disruptive cognitive and psychological symptoms (CPS), such as agitation, oppositional behavior, or excessive wandering;\n* Free and informed consent to participate in the study, signed by the participant or their legal representative.\n\nExclusion Criteria:\n\n* Lack of affiliation to a health insurance or social security scheme;\n* Life expectancy of less than three months;\n* Inability to obtain a signed informed consent form from the resident or their legal representative","ALL","65 Years",{"count":19,"type":20},226,"ESTIMATED","INTERVENTIONAL",[23],"NA","To evaluate, by comparison with the classical method, the effectiveness of using the TNmP method in reducing the intensity or frequency of behavioral disorders in elderly people institutionalized in an institution.",[26],"Personalized Non-pharmacological Therapies","NOT_YET_RECRUITING","2026-02-24",{"date":30,"type":31},"2026-02-27","ACTUAL",{"date":33,"type":20},"2026-04-05",{"date":35,"type":20},"2027-04-05",{"name":37,"class":38},"Centre Médical Porte Verte","OTHER",{"id":40,"slug":4,"hasResults":10,"nctId":41,"briefTitle":42,"officialTitle":42,"acronym":43,"eligibilityCriteria":44,"healthyVolunteers":10,"sex":16,"minAge":45,"maxAge":4,"enrollmentInfo":46,"targetDuration":4,"studyType":21,"phases":48,"briefSummary":49,"conditions":50,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":52,"lastUpdatePostDateStruct":53,"startDateStruct":55,"completionDateStruct":57,"leadSponsor":59,"locationsCount":4},"100591846","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","70 Years",{"count":47,"type":20},50,[23],"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.",[51],"Virtual Reality","2025-05-22",{"date":54,"type":31},"2025-05-28",{"date":56,"type":20},"2025-09-01",{"date":58,"type":20},"2026-09-01",{"name":37,"class":38},{"id":61,"slug":4,"hasResults":10,"nctId":62,"briefTitle":63,"officialTitle":64,"acronym":65,"eligibilityCriteria":66,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":67,"targetDuration":4,"studyType":68,"phases":4,"briefSummary":69,"conditions":70,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":74,"completionDateStruct":75,"leadSponsor":77,"locationsCount":4},"100591845","NCT06985719","Effectiveness of Adapted Physical Activity Programs in Preventing Falls in People Aged Over 65","Effectiveness of Adapted Physical Activity Programs in Preventing Falls in People Aged Over 65: a Prospective Multicenter Study Carried Out Within the Maisons Sport Santé of Ile de France Departement","APA-SAFE","Inclusion Criteria:\n\n* People at risk of falling People practicing an APA program for 3 months Persons who have given their consent to participate in the study\n\nExclusion Criteria:\n\n* Patient refusal to participate in the study Absolute or relative contraindication to APA Persons under guardianship Non-affiliation to a social security scheme",{"count":47,"type":20},"OBSERVATIONAL","The objective of this study is to evaluate the effectiveness of Adapted Physical Activity (APA) programs offered by Sport-Health Centers (MSS) in reducing the risk of falls in the elderly.",[71],"Adapted Physical Activity","2025-05-21",{"date":52,"type":31},{"date":56,"type":20},{"date":76,"type":20},"2025-12-30",{"name":37,"class":38},""]