[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100599402":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":19,"centralContacts":20,"locations":30,"responsibleParty":48,"collaborators":19,"id":50,"slug":51,"hasResults":52,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":56,"eligibilityCriteria":57,"healthyVolunteers":58,"sex":59,"minAge":60,"maxAge":19,"enrollmentInfo":61,"targetDuration":19,"studyType":64,"phases":65,"briefSummary":67,"conditions":68,"keywords":71,"overallStatus":33,"whyStopped":19,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":85,"locationsCount":86},{"fullName":5,"class":6},"University Hospital, Toulouse","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Perceive, Recall, Plan and Perform-Intervention (PRPP-I)","EXPERIMENTAL","task-based cognitive strategy training during activities appropriate for delivery in home-based setting.",[13],"Other: Perceive, Recall, Plan and Perform-Intervention protocol (PRPP-I)",[15],{"type":6,"name":16,"description":17,"armGroupLabels":18,"otherNames":19},"Perceive, Recall, Plan and Perform-Intervention protocol (PRPP-I)","delivered over a 4-week period, in 12 sessions (45\u002F60 min, 3 days a week for 4 weeks) for all patients according to the PRPP-I protocol. The intervention will be carried out by a PRPP-certified occupational therapist working on a Master's degree.\n\nIt will consist of :\n\n* Implementation of training in functional cognitive strategies and meta-prompts through performance in home activities,\n* Repeated measurement of performance judgment criteria ;\n* Assessment of cognitive strategies\n* personalized implementation of the PRPP-I cognitive strategy training protocol.\n* Collection of feasibility modalities when tracking the intervention (e.g., time, transport, etc.).",[9],null,[21,26],{"name":22,"role":23,"phone":24,"phoneExt":19,"email":25},"Margot MORIN","CONTACT","05 61 77 73 47","morin.mar@chu-toulouse.fr",{"name":27,"role":23,"phone":28,"phoneExt":19,"email":29},"Clémence Le Bervet","0561777087","drci.toulouse@chu-toulouse.fr",[31],{"facility":32,"status":33,"city":34,"state":19,"zip":19,"country":35,"countryCode":36,"cosmosGeoPoint":37,"geoPoint":42,"contacts":43},"University Hospital of Toulouse","RECRUITING","Toulouse","France","FR",{"type":38,"coordinates":39},"Point",[40,41],1.44367,43.60426,{"lat":41,"lon":40},[44],{"name":45,"role":23,"phone":46,"phoneExt":19,"email":47},"Claire VILLEPINTE, MD","(+33 5 67 7)7 17 24","villepinte.c@chu-toulouse.fr",{"type":49,"investigatorFullName":19,"investigatorTitle":19,"investigatorAffiliation":19,"oldNameTitle":19,"oldOrganization":19},"SPONSOR","100599402","home-based-cognitive-strategy-training-for-daily-living-in-adults-with-chronic-stroke-100599402",false,"NCT07084025","Home-based Cognitive Strategy Training for Daily Living in Adults With Chronic Stroke","Feasibility of Home-based Cognitive Strategy Training for Independence of Activities of Daily Living in Adults With Chronic Stroke","PRPP-HOME","Patient's Main Eligibility criteria:\n\n* Adult over 18 years of age;\n* cognitive deficits (or Acquired Brain Injury) diagnosed due to ischemic or hemorrhagic, hemispheric or brainstem stroke, confirmed by brain imaging longer than 6 months;\n* Patient with mild (\\\u003C26\u002F30 or \\\u003C25\u002F30 for patients aged 71-85 yr) or moderate (\\[18-25\\]\u002F30) cognitive impairment, measured by the Montreal Cognitive Assessment test ;\n* adults living in a home or community-based setting;\n* Patient with a non-professional caregiver;\n\nPatient's Main Exclusion criteria\n\n* Neurological pathology other than stroke or psychiatric disorder;\n* Significant cognitive impairment, according to MoCA score \\\u003C18\u002F30;\n* Patient with severe aphasia, Boston Diagnostic Aphasia Examination score \\>2",true,"ALL","18 Years",{"count":62,"type":63},18,"ESTIMATED","INTERVENTIONAL",[66],"NA","This pilot experimental study aims to describe the feasibility of a cognitive strategy training protocol : PRPP-I, in activities of daily life across home-based setting for adults with chronic stroke for improvement of independence and quality of life. Aditionnally to examine preliminary effectiveness of PRPP-I protocol within a home-based setting on functional cognitive strategies, independence, quality of life and career burden.",[69,70],"Stroke","Cerebrovascular Disorders",[72,73,74,75,76],"Cognitive strategy training","Task-based","Ecological","Performance","Activities of Daily Living","2026-05-07",{"date":79,"type":80},"2026-05-08","ACTUAL",{"date":82,"type":80},"2026-01-05",{"date":84,"type":63},"2027-12-31",{"name":5,"class":6},1]