[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"dual-task-exercises-in-elderly-people\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:dual-task-exercises-in-elderly-people":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,43],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100627463","individualized-dual-task-training-for-balance-and-mobility-in-older-adults-100627463",false,"NCT07448961","INDIVIDUALIZED DUAL-TASK TRAINING FOR BALANCE AND MOBILITY IN OLDER ADULTS","EFFECTS OF SENSORİAL AND COGNİTİVE INDİVİDUALİZED DUAL-TASK TRAİNİNG ON FUNCTİONAL BALANCE, MOBİLİTY, AND DUAL-TASK PERFORMANCE İN OLDER ADULTS: A RANDOMİZED CONTROLLED TRİAL","Inclusion Criteria:\n\n* Aged 65 years and older.\n* Living independently in the community.\n* Ability to walk at least 10 meters without the use of an assistive device (e.g., cane, walker).\n* Cognitively intact, defined as a Montreal Cognitive Assessment (MoCA) score of 24 or higher.\n* Stable medical condition allowing for participation in an 8-week exercise program.\n* Willingness to participate in the study and provide written informed consent.\n\nExclusion Criteria:\n\n* History of neurological disorders affecting movement or cognition (e.g., Stroke, Parkinson's Disease, Dementia).\n* Acute or chronic orthopedic conditions that severely limit gait or balance (e.g., recent lower limb fracture or major joint replacement within the last 6 months).\n* Severe visual or hearing impairment that prevents following instructions or performing tasks.\n* Uncontrolled cardiovascular or pulmonary disease.\n* Currently participating in another structured exercise or dual-task training program.\n* Inability to commit to the 8-week training schedule.",true,"ALL","65 Years",{"count":20,"type":21},48,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this clinical trial is to prevent functional decline and improve mobility in healthy older adults aged 65 and over. The main questions it aims to answer are:\n\nWhat is the effect of individualized dual-task training on functional balance and mobility compared to standard training? Does personalized sensory and cognitive training significantly reduce the dual-task cost during walking tasks? Researchers will compare the Individualized Dual-Task Group to a Standardized Dual-Task Group and a Single-Task Control Group to see if personalized adjustments in sensory and cognitive loads lead to superior improvements in balance, gait speed, and motor-cognitive interference.\n\nParticipants will:\n\nComplete an initial assessment of motor and cognitive capacities to determine individual baseline levels.\n\nParticipate in a supervised exercise program 3 days a week for 8 weeks, with each session lasting 40-45 minutes.\n\nPerform motor tasks such as walking, obstacle crossing, and balance exercises while simultaneously engaging in cognitive tasks (e.g., counting, verbal fluency).\n\n(For the individualized group) Undergo weekly adjustments in exercise difficulty, including sensory manipulations like surface changes and head movements based on their performance.",[27,28,29,30],"Healthy Older Adults","Postural Balance","Dual Task Exercises in Elderly People","Dual Task Cost","RECRUITING","2026-04-29",{"date":34,"type":35},"2026-05-05","ACTUAL",{"date":32,"type":35},{"date":38,"type":21},"2027-04",{"name":40,"class":41},"Sezen Karaborklu Argut","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":50,"targetDuration":4,"studyType":22,"phases":52,"briefSummary":53,"conditions":54,"keywords":58,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":4},"100608704","freefrail-project-a-multicomponent-intervention-for-the-management-of-frailty-in-primary-care-a-randomized-controlled-trial-100608704","NCT07205016","FreeFrail Project: A Multicomponent Intervention for the Management of Frailty in Primary Care: A Randomized Controlled Trial","FreeFrail Project: Effectiveness of a Multicomponent Intervention Including Dual-task Exercise to Increase Functionality and Cognitive Performance in Frail and Pre-frail Individuals Over 65 Years Aged in Primary Care Compared to Usual Care: Protocol for a Randomized Controlled Trial","Inclusion Criteria:\n\n* Aged 65 or older\n* Frailty according to Fragil-VIG index (\\>0,20)\n* Barthel index \\> 60\n* Able to perform physical exercise\n* Able to understand and communicate in Catalan or Spanish\n\nExclusion Criteria:\n\n* Decompensated \u002F Unstable cardiovascular disease or recent diagnosed\n* Upper or lower injury with functional impairment\n* Institutionalized patient.\n* Terminal or tumoral processes\n* People who participated in another clinical trial or exercise programme during last year\n* Diagnosis of severe dementia",{"count":51,"type":21},220,[24],"The primary aim is to assess the effectiveness of a multicomponent intervention including dual-task exercise in improving functionality and cognitive performance and in reducing frailty among community-dwelling adults aged ≥65 years compared to usual care. Secondary objectives include evaluating its impact on pain, anxiety or depression, sleep quality, quality of life, physical activity, handgrip strength, and polypharmacy.\n\nA double-blind, randomized, parallel-group controlled trial will be conducted in primary care centers in Lleida. Frail older adults (≥65 years) will be recruited and randomly allocated to either the intervention group, receiving a structured cognitive-motor dual-task based multicomponent program, or the control group, receiving usual care. Outcomes will be assessed using validated tools at baseline and follow-up.",[55,29,56,57],"Frail Elderly","Exercise Training","Frailty",[59,60,61,62,63,64],"primary care Health [MeSH]","multicomponent intervention","exercise therapy [MeSH]","cognitive-motor dual-task","frail elderly [MeSH]","frailty [MeSH]","NOT_YET_RECRUITING","2025-09-24",{"date":68,"type":35},"2025-10-03",{"date":70,"type":21},"2026-01",{"date":72,"type":21},"2026-10",{"name":74,"class":41},"Universitat de Lleida"]