[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100354387":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":25,"locations":30,"responsibleParty":98,"collaborators":19,"id":100,"slug":101,"hasResults":102,"nctId":103,"briefTitle":104,"officialTitle":105,"acronym":106,"eligibilityCriteria":107,"healthyVolunteers":102,"sex":108,"minAge":109,"maxAge":19,"enrollmentInfo":110,"targetDuration":19,"studyType":113,"phases":114,"briefSummary":116,"conditions":117,"keywords":19,"overallStatus":33,"whyStopped":19,"lastUpdateSubmitDate":119,"lastUpdatePostDateStruct":120,"startDateStruct":123,"completionDateStruct":125,"leadSponsor":127,"locationsCount":128},{"fullName":5,"class":6},"Hospices Civils de Lyon","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Patients with subjective cognitive complaint or neurocognitive","EXPERIMENTAL",": Real-life cohort patients with subjective cognitive complaint or neurocognitive disorders undergoing medical examination in memory centers, and for whom extensive evaluations will be performed for the study",[13],"Other: no intervention",[15],{"type":6,"name":16,"description":17,"armGroupLabels":18,"otherNames":19},"no intervention","This is study carried out in current practice. Patients are undergoing a medical examination in a memory center, with extensive and systematic evaluations for the study involving the following tests: IADL, DAD6, New AGGIR, NPI, and mini-Zarit) assessing the functions (autonomy, behavior and caregiver burden).",[9],null,[21],{"name":22,"affiliation":23,"role":24},"Pierre Krolak-Salmon, PhD","Centre Mémoire de Ressources et de Recherche","PRINCIPAL_INVESTIGATOR",[26],{"name":22,"role":27,"phone":28,"phoneExt":19,"email":29},"CONTACT","04 72 43 20 50","pierre.krolak-salmon@chu-lyon.fr",[31,50,64,73,87],{"facility":32,"status":33,"city":34,"state":19,"zip":35,"country":36,"countryCode":37,"cosmosGeoPoint":38,"geoPoint":43,"contacts":44},"Hôpital Dugoujon","RECRUITING","Caluire-et-Cuire","69300","France","FR",{"type":39,"coordinates":40},"Point",[41,42],4.8464,45.79462,{"lat":42,"lon":41},[45],{"name":46,"role":27,"phone":47,"phoneExt":48,"email":49},"Sylvain Gaujard, MD","04 72 00 15 32","+33","sylvain.gaujard@chu-lyon.fr",{"facility":51,"status":33,"city":52,"state":19,"zip":53,"country":36,"countryCode":37,"cosmosGeoPoint":54,"geoPoint":58,"contacts":59},"Centre Hospitalier Lyon Sud","Lyon","69310",{"type":39,"coordinates":55},[56,57],4.84789,45.74906,{"lat":57,"lon":56},[60],{"name":61,"role":27,"phone":62,"phoneExt":19,"email":63},"Marc Bonnefoy, PhD","04 78 86 15 81","marc.bonnefoy@chu-lyon.fr",{"facility":65,"status":33,"city":52,"state":19,"zip":19,"country":36,"countryCode":37,"cosmosGeoPoint":66,"geoPoint":68,"contacts":69},"Service de neuro-cognition et neuro-ophtalmologie du Groupement Hospitalier Est",{"type":39,"coordinates":67},[56,57],{"lat":57,"lon":56},[70],{"name":71,"role":27,"phone":19,"phoneExt":19,"email":72},"Virginie Desestret, PhD","virginie.desestret@chu-lyon.fr",{"facility":74,"status":33,"city":75,"state":19,"zip":76,"country":36,"countryCode":37,"cosmosGeoPoint":77,"geoPoint":81,"contacts":82},"CHU Saint-Etienne","Saint-Etienne","42055",{"type":39,"coordinates":78},[79,80],4.39,45.43389,{"lat":80,"lon":79},[83],{"name":84,"role":27,"phone":85,"phoneExt":19,"email":86},"Jean-Claude Getenet, MD","04 77 12 78 05","j.claude.getenet@chu-st-etienne.fr",{"facility":88,"status":33,"city":89,"state":19,"zip":90,"country":36,"countryCode":37,"cosmosGeoPoint":91,"geoPoint":95,"contacts":96},"Centre Mémoire de Ressources et de Recherche de Lyon","Villeurbanne","69100",{"type":39,"coordinates":92},[93,94],4.8795,45.76601,{"lat":94,"lon":93},[97],{"name":22,"role":27,"phone":28,"phoneExt":19,"email":29},{"type":99,"investigatorFullName":19,"investigatorTitle":19,"investigatorAffiliation":19,"oldNameTitle":19,"oldOrganization":19},"SPONSOR","100354387","predictive-factors-of-autonomy-loss-in-real-life-cohort-100354387",false,"NCT03894254","Predictive Factors of Autonomy Loss in Real-life Cohort","Predictive Factors Associated With Impairment in Functional Autonomy in a Regional Real-life Cohort of Patients With Alzheimer's Disease or Related Disorders (ADRD)","MEM-AURA","Inclusion Criteria:\n\n* Patients aged 18 years and older, undergoing a medical visit in a memory center or neuro-cognition service\n* Patients living at home or in housing\n* Patients with memory impairment, at all stage of the disease\n\nExclusion Criteria:\n\n* Patients in institution\n* Patients under legal protection\n* Patients with a hearing or visual impairment, which prevents carrying out examinations","ALL","18 Years",{"count":111,"type":112},5400,"ESTIMATED","INTERVENTIONAL",[115],"NA","The Alzheimer's disease or related disorders (ADRD) are among the most disabling diseases because of their main features such as cognitive impairment, loss of functional autonomy and behavioural disorders. In absence of current curative treatment, the identification of the predictive risk factors of progression of the disease, evaluated through its main symptoms, represents a major stake of public health. The Investigators aim at developing a regional database, which includes the patient medical records on a prospective basis, in collaboration with the medical and administrative staff and with the University hospital computer science departments.\n\nThe main objective is to study the predictive factors associated with change in functional autonomy level, measured every 6 to 12 months in centres across Region Auvergne Rhone-Alpes in France.\n\nThe real-life study population will consist in about 5400 patients with ADRD. The inclusion period will be of 3 years, the length of follow-up of each patient will be of 10 years max for a total study length of 13 years.",[118],"Memory Disorders","2022-04-25",{"date":121,"type":122},"2022-05-02","ACTUAL",{"date":124,"type":122},"2020-09-09",{"date":126,"type":112},"2032-03-01",{"name":5,"class":6},5]