[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"I-Shou University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":91},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,43,71],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100652958","the-effect-of-an-aiot-based-smart-exercise-system-in-older-adults-100652958",false,"NCT07779824","The Effect of an AIoT-Based Smart Exercise System in Older Adults","Development of a Precision Exercise System for Older Adults and People With Stroke Using Deep Learning and Facial Action Units","Inclusion Criteria:\n\n* Adult over 50 years old\n* No significant limb disability or joint deformation\n* No history of cardiovascular disease\n* Never lost balance due to dizziness in the past 12 months\n\nExclusion Criteria:\n\n* Limb disability or joint deformation\n* History of cardiovascular disease\n* Lost balance due to dizziness in the past 12 months\n* Cognitive deficits","ALL","50 Years",{"count":19,"type":20},200,"ESTIMATED","INTERVENTIONAL",[23],"NA","This clinical trial aims to evaluate the effectiveness of an artificial intelligence of things (AIoT)-based exercise system for seniors. Participants will undergo a 12-week AIoT-based cycle ergometer training program. Physical fitness and functional performance will be assessed at baseline and after completion of the intervention. Throughout the intervention, exercise-related data, including exercise duration, workload, heart rate, oxygen consumption, perceived exertion, and facial expressions, will be continuously and simultaneously collected for analysis.",[26,27],"Exercise","Seniors",[27,26,29],"facial action unit","RECRUITING","2026-08-18",{"date":33,"type":34},"2026-08-21","ACTUAL",{"date":36,"type":34},"2026-02-20",{"date":38,"type":20},"2028-07-31",{"name":40,"class":41},"I-Shou University","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":16,"minAge":50,"maxAge":51,"enrollmentInfo":52,"targetDuration":4,"studyType":21,"phases":54,"briefSummary":55,"conditions":56,"keywords":60,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":42},"100617873","hybrid-stroke-rehab-with-mirror-priming-100617873","NCT07324278","Hybrid Stroke Rehab With Mirror Priming","Hybrid Stroke Rehabilitation With Mirror Priming","Inclusion Criteria:\n\n1. A first-ever unilateral stroke ≥3 months\n2. Age between 20 and 80 years\n3. Baseline Fugl-Meyer Assessment Upper Extremity (FMA-UE) score \\>10\n4. No severe spasticity in any joints of the affected arm\n5. Ability to follow the instructions\n6. No participation in other studies during the study period\n7. Willingness to provide informed written consent.\n\nExclusion Criteria:\n\n1\\. Serious medical problems or poor physical conditions that might be detrimental to study participation.","20 Years","80 Years",{"count":53,"type":20},81,[23],"This trial aims to examine the effects of enhanced mirror priming, overcoming the limitations of traditional mirror therapy, to achieve optimization and personalized intervention.",[57,58,59],"Cardiovascular Diseases","Stroke","Cerebrovascular Disorders",[61,62],"Rehabilitation","Mirror Therapy","2025-12-23",{"date":65,"type":34},"2026-01-07",{"date":67,"type":20},"2025-12-30",{"date":69,"type":20},"2030-12-31",{"name":40,"class":41},{"id":72,"slug":73,"hasResults":11,"nctId":74,"briefTitle":75,"officialTitle":76,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":16,"minAge":50,"maxAge":51,"enrollmentInfo":77,"targetDuration":4,"studyType":21,"phases":79,"briefSummary":80,"conditions":81,"keywords":82,"overallStatus":83,"whyStopped":4,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":90,"locationsCount":4},"100553734","mirror-therapy-combined-with-task--vs-impairment-oriented-rehabilitation-program-100553734","NCT06489938","Mirror Therapy Combined With Task- vs. Impairment-oriented Rehabilitation Program","Effect of Mirror Therapy Combined With Task- vs. Impairment-oriented Rehabilitation Program in Individuals With Stroke",{"count":78,"type":20},123,[23],"The goal of this clinical trial is to examine the effects of mirror therapy combined with task- vs. Impairment-oriented rehabilitation programs as novel hybrid approaches in individuals with stroke. Participants will receive mirror therapy combined with the task-oriented rehabilitation program (MTT), mirror therapy combined with the impairment-oriented rehabilitation program (MTI), or task-oriented rehabilitation program combined with the impairment-oriented rehabilitation program (TI) 90 minutes per day, three days per week, for six weeks.",[57,58,59],[61,62],"NOT_YET_RECRUITING","2024-06-29",{"date":86,"type":34},"2024-07-08",{"date":88,"type":20},"2024-07-01",{"date":69,"type":20},{"name":40,"class":41},""]