[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100626023":3},{"organization":4,"armGroups":7,"interventions":13,"overallOfficials":17,"centralContacts":18,"locations":17,"responsibleParty":28,"collaborators":17,"id":32,"slug":33,"hasResults":34,"nctId":35,"briefTitle":36,"officialTitle":37,"acronym":38,"eligibilityCriteria":39,"healthyVolunteers":34,"sex":40,"minAge":41,"maxAge":17,"enrollmentInfo":42,"targetDuration":17,"studyType":45,"phases":46,"briefSummary":48,"conditions":49,"keywords":17,"overallStatus":51,"whyStopped":17,"lastUpdateSubmitDate":52,"lastUpdatePostDateStruct":53,"startDateStruct":56,"completionDateStruct":58,"leadSponsor":60,"locationsCount":17},{"fullName":5,"class":6},"Centre Médical Porte Verte","OTHER",[8],{"label":9,"type":6,"description":10,"interventionNames":11},"before\u002Fafter study","To evaluate the effectiveness of the TNmP method in reducing the intensity and\u002For frequency of behavioral disturbances by comparing two groups of centers (four using the conventional PNPT selection method and six using the TNmP method).",[12],"Other: TNmP",[14],{"type":6,"name":15,"description":10,"armGroupLabels":16,"otherNames":17},"TNmP",[9],null,[19,24],{"name":20,"role":21,"phone":22,"phoneExt":17,"email":23},"Valérie BRENIERE, Dr","CONTACT","01 81 70 51 97","valerie.breniere@univi.fr",{"name":25,"role":21,"phone":26,"phoneExt":17,"email":27},"Fatima IZEDAREN","0139637451","fatima-zohra.izedaren@lpv.univi.fr",{"type":29,"investigatorFullName":30,"investigatorTitle":31,"investigatorAffiliation":5,"oldNameTitle":17,"oldOrganization":17},"PRINCIPAL_INVESTIGATOR","Valérie BRENIERE","Principal Investigator","100626023","impact-of-implementing-the-personalized-non-pharmacological-therapies-method-in-facilities-for-the-elderly-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":43,"type":44},226,"ESTIMATED","INTERVENTIONAL",[47],"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.",[50],"Personalized Non-pharmacological Therapies","NOT_YET_RECRUITING","2026-02-24",{"date":54,"type":55},"2026-02-27","ACTUAL",{"date":57,"type":44},"2026-04-05",{"date":59,"type":44},"2027-04-05",{"name":5,"class":6}]