[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"elderly-person\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:elderly-person":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,47,71],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":31,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100469153","finger-food-pleasure-at-your-fingertips-randomized-pilot-study-open-label-and-parallel-groups-100469153",false,"NCT05389098","Finger Food, Pleasure at Your Fingertips: Randomized Pilot Study, Open-label and Parallel Groups","L'Alimentation Manger-mains, le Plaisir au Bout Des Doigts : Etude Pilote randomisée, en Ouvert et en Groupes parallèles","PLAID","Inclusion Criteria:\n\n* Male or female residents over 75 years old living in a Accommodation facility for dependent elderly people for at least 3 months\n* Presenting at least one of the following 3 criteria:\n\n  * Unintentional weight loss ≥ 5% in 1 month\n  * Involuntary weight loss ≥ 10% in 6 months or compared to the usual weight or compared to the weight at entry to the EHPAD\n  * Confirmed sarcopenia:\n\n    * Male (at least one of the 2 criteria):\n\n      * Dynamometer (kg): \\\u003C 27 AND calf circumference (cm): \\\u003C 31\n      * Impedancemetry: appendicular muscle mass index \\\u003C 20 kg OR appendicular muscle mass index \\\u003C 7 kg\u002Fm²\n    * Woman (at least one of the 2 criteria):\n\n      * Dynamometer (kg): \\\u003C 16 AND calf circumference (cm): \\\u003C 31\n      * Impedancemetry: appendicular muscle mass index \\\u003C 15 kg OR appendicular muscle mass index \\\u003C 5.5 kg\u002Fm²\n* Loss of autonomy according to the Tully scale \\\u003C 12\u002F18 with a score of 2 or 3 on the item \"Able to bite, chew, swallow without making false routes\"\n* Person having given free, informed and express consent\n* Person having an affiliation to a social security scheme\n\nExclusion Criteria:\n\n* Protected person: safeguard of justice\n* Swallowing disorder having a contra-indication to the texture of hand-eating meals.\n* Lack of motor skills in both hands\n* Specific diet: pleasure diet, salt-free, sugar-free, fiber-free, artificial nutrition\n* Wearer of a pacemaker",true,"ALL","75 Years","120 Years",{"count":22,"type":23},30,"ESTIMATED","INTERVENTIONAL",[26],"NA","Food is available in easy-to-grip bites that allow residents in care settings to use their fingers for food. This new way of eating can help limit weight loss, increase food intake, gain independence and improve the enjoyment of eating for residents.",[29,30],"Undernutrition","Elderly Person",[29,30,32,33],"Nursing home","Nutrition","RECRUITING","2025-11-18",{"date":37,"type":38},"2025-11-24","ACTUAL",{"date":40,"type":38},"2023-08-03",{"date":42,"type":23},"2027-01-31",{"name":44,"class":45},"University Hospital, Tours","OTHER",2,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":24,"phases":56,"briefSummary":58,"conditions":59,"keywords":4,"overallStatus":61,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":4},"100575635","phase-3-aspirin-in-acute-pneumonia-in-the-elderly-a-multicenter-double-blind-randomized-placebo-controlled-trial-100575635","NCT06774846","Aspirin in Acute Pneumonia in the Elderly: a Multicenter, Double-blind, Randomized, Placebo-controlled Trial.","ASPAPY","Inclusion Criteria:\n\n* Informed consent obtained from patient or relative\u002Ftrusted person if patient unable to consent\n* Age ≥75 years\n* Clinical diagnosis of AP, presumed to be of bacterial or viral origin, with at least two of the following signs or symptoms:\n* cough,\n* purulent expectoration,\n* thoracic pain,\n* dyspnea\u002Ftachypnea,\n* temperature \\> 37.8°C or \\\u003C 36°C,\n* unilateral crackles\n* Patient hospitalized for at least 48 hours\n* Onset of clinical signs \\\u003C 7 days\n* New radiological infiltrate documented by X-ray, ultrasound or CT scan\n\nExclusion Criteria:\n\n* Mechanically ventilated pneumonia\n* Documented SARS CoV2 pneumonia\n* Patient with at least 3 episodes of inhalation pneumonitis in the 12 months prior to inclusion\n* Pre-acute episode swallowing disorders impairing oral medication intake\n* Physician-assessed life expectancy \\\u003C 90 days\n* Anticoagulant treatment (curative doses)\n* Antiplatelet therapy\n* Steroidal or non-steroidal anti-inflammatory treatment or oral corticosteroids without proton pump inhibitor (PPI)\n* Treatment with methotrexate (\\>20 mg per week), anagrelide, probenecid, nicorandil, defibrotide\n* Dyspepsia or gastroesophageal reflux disease (GERD) without PPI use\n* Contraindications to aspirin (preventive doses) or its placebo at the time of inclusion:\n* Hypersensitivity to acetylsalicylic acid or to any of the excipients of the investigational drug or placebo\n* History of asthma induced by the administration of salicylates or non-steroidal anti-inflammatory drugs\n* Active peptic ulcer disease or history of recurrent peptic ulcer disease\n* History of cerebrovascular haemorrhage\n* Previous gastrointestinal hemorrhage\n* History of hemorrhage with Hemoglobin \\> 3g \u002Fdl requiring transfusion, vasoactive treatment or surgery\n* Known hereditary or acquired coagulation disorder\n* Thrombocytopenia (platelets \\\u003C 50 giga\u002FL)\n* Acute kidney injury (clairance \\\u003C 15 ml\u002Fmin selon MDRD - Modification of Diet in Renal Disease),\n* Liver cirrhosis or acute liver failure (PTT\\\u003C50%),\n* Severe uncontrolled heart failure\n* Persistente severe hypertension (PAS \\> 180mmHg)\n* Patient with mastocytosis\n* Person not affiliated to a national social security scheme\n* Patient under court protection",{"count":55,"type":23},600,[57],"PHASE3","Acute pneumonia is a very common disease, and one of the leading causes of hospitalization and death in France. Almost a century after the discovery of penicillin, no major breakthrough has significantly reduced pneumonia-related mortality. While the choice of an appropriate antibiotic is decisive in the acute phase of the disease, the longer-term prognosis depends essentially on the worsening of other underlying pathologies, particularly in the elderly. In cured patients, excess mortality persists several months after the episode of pneumonia, due in particular to the onset of cardiovascular complications. Recent scientific literature shows an association between the prescription of cardio-protective drugs and survival after pneumonia. Older patients are usually excluded from interventional studies, so there are no specific recommendations for these patients at high risk of both acute pneumonia and cardiovascular events.\n\nThe aim of this study is to assess the efficacy of low-dose aspirin therapy after pneumonia in preventing cardiovascular events in the elderly.\n\nThe main objective is therefore to evaluate the impact of aspirin at a dose of 100mg per day on all-cause mortality at 90 days in patients over 75 years of age hospitalized for pneumonia.",[60,30],"Acute Pneumonia","NOT_YET_RECRUITING","2025-09-11",{"date":64,"type":38},"2025-09-12",{"date":66,"type":23},"2026-02",{"date":68,"type":23},"2029-06",{"name":70,"class":45},"Centre Hospitalier Universitaire Dijon",{"id":72,"slug":73,"hasResults":11,"nctId":74,"briefTitle":75,"officialTitle":76,"acronym":77,"eligibilityCriteria":78,"healthyVolunteers":11,"sex":18,"minAge":79,"maxAge":80,"enrollmentInfo":81,"targetDuration":4,"studyType":24,"phases":83,"briefSummary":84,"conditions":85,"keywords":88,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":90,"lastUpdatePostDateStruct":91,"startDateStruct":93,"completionDateStruct":95,"leadSponsor":97,"locationsCount":46},"100544153","evaluation-of-the-concordance-of-five-times-sit-to-stand-results-between-a-physical-consultation-and-a-teleconsultation-100544153","NCT06365177","Evaluation of the Concordance of Five Times Sit To Stand Results Between a Physical Consultation and a Teleconsultation","Evaluation of the Concordance of Five Times Sit To Stand Results Between a Physical Consultation and a Teleconsultation of the Elderly","TELETEST","Inclusion Criteria:\n\n* Volunteers over the age of 65.\n* Elderly people who can walk and move around independently.\n* Subjects capable of giving informed consent.\n* GIR 3,4,5,6.\n* Affiliated to a Social Security scheme.\n\nExclusion Criteria:\n\n* GIR \\\u003C 3\n* Major visual and\u002For hearing impairment (known pathology and not fitted with hearing aids)\n* Patient deprived of liberty by judicial or administrative decision, under guardianship or curatorship\n* Subject having refused to participate.\n* Subject at risk of syncope on rising (cardiac pathologies, orthostatic hypotension).\n* Subjects with known vestibular disorders.","65 Years","110 Years",{"count":82,"type":23},108,[26],"This study concerns elderly person aged more than 65 years with autonomous mobility.\n\nIt is a multicentric randomized trial in two arms :\n\nArm one : remote consultation then physical consultation Arm two : physical consultation then remote consultation\n\nConsultations consist to take a Five Times Sit To Stand test, in physical consultation with physiotherapist in the same room and in remote consultation with a physiotherapist in the next room to the patient.",[86,30,87],"Rehabilitation","Teleconsultation",[89,87],"Five Time Sit To Stand","2024-07-03",{"date":92,"type":38},"2024-07-05",{"date":94,"type":38},"2024-06-20",{"date":96,"type":23},"2026-12-20",{"name":98,"class":45},"University Hospital, Brest"]