[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"upper-limb-rehabilitation\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:upper-limb-rehabilitation":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,45,79],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100343525","exoneuromusculoskeleton-for-upper-limb-rehabilitation-after-stroke-100343525",false,"NCT03752775","Exoneuromusculoskeleton for Upper Limb Rehabilitation After Stroke","Mobile Electromyography (EMG)-Driven Exoneuromusculoskeleton for Upper Limb Rehabilitation After Stroke","Inclusion Criteria:\n\nFor the subacute groups:\n\n* Two weeks after the onset of stroke, however less than 0.5 year\n* Mini-Mental State Examination (MMSE)\\>21\n* Able to sit up for at least 1 hour\n* Fugl-Meyer Assessment (FMA) upper limb \\\u003C30\n* Modified Ashworth Score (MAS) at the elbow, wrist and fingers \\\u003C3\n* Detectable EMG on the target driving muscles (i.e., 3 times of the standard deviation above the baseline)\n\nFor the chronic device assisted group:\n\n* At least 0.5 year after the onset of stroke\n* Mini-Mental State Examination (MMSE)\\>21\n* Able to sit up for at least 1 hour\n* Fugl-Meyer Assessment (FMA) upper limb \\\u003C30\n* Modified Ashworth Score (MAS) at the elbow, wrist and fingers \\\u003C3\n* Detectable EMG on the target driving muscles (i.e., 3 times of the standard deviation above the baseline)\n\nExclusion Criteria:\n\nSubjects will be excluded if they do not meet the above inclusion criteria, or had the following conditions:\n\n* Currently pregnant\n* Dysphasia (language deficiency)\n* Post-stroke neglect\n* Pacemaker implantation,\n* Involved in drug studies, other clinical trials, or concurrent medication\u002Foccupational\u002Fphysical treatments on the upper limb\n* The overall medical condition not suitable for the training (e.g., severe cardiac problem, unstable blood pressure, etc.).","ALL","18 Years","70 Years",{"count":20,"type":21},45,"ESTIMATED","INTERVENTIONAL",[24],"NA","A new clothing robotic arm was developed for multi-joint coordinated upper limb rehabilitation after stroke. Patients after stroke will be recruited to evaluate the rehabilitation effectiveness of the device assisted upper limb rehabilitation. Both patients with chronic stroke and subacute stroke will be investigated.",[27],"Upper Limb Rehabilitation",[29,30,31],"stroke","upper limb","Joint coordination","RECRUITING","2026-06-18",{"date":35,"type":36},"2026-06-23","ACTUAL",{"date":38,"type":36},"2018-11-01",{"date":40,"type":21},"2027-12-31",{"name":42,"class":43},"The Hong Kong Polytechnic University","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":22,"phases":55,"briefSummary":56,"conditions":57,"keywords":61,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":78},"100608266","clinical-validation-of-an-ai-based-decision-support-system-for-robotic-upper-limb-rehabilitation-in-patients-with-stroke-a-co-aider-study-100608266","NCT07199322","Clinical validatiOn of an AI-based DEcision Support System for Robotic Upper Limb Rehabilitation in Patients With Stroke. A CO-AIDER Study.","COAIDER","Inclusion Criteria:\n\n* Diagnosis of ischemic or hemorrhagic stroke confirmed by Computed Tomography (CT) or Magnetic Resonance Imaging (MRI);\n* Age between 18 and 85 years;\n* Time since stroke less than six months;\n* Mild to severe upper limb impairment (Fugl-Meyer Assessment for Upper Extremity (FMA-UE) ≤ 58).\n\nExclusion Criteria:\n\n* Behavioral or cognitive disorders and\u002For reduced compliance;\n* Severe spasticity or hypertonia in the affected limb (Modified Ashworth Scale (MAS) \\> 3);\n* Severe visual impairments;\n* Concurrent participation in another clinical trial for upper limb rehabilitation following stroke;\n* Refusal to provide written informed consent.","85 Years",{"count":54,"type":21},100,[24],"The goal of this clinical trial is to validate an artificial intelligence-based decision support system (AI-DSS) for robotic rehabilitation in participants with stroke.\n\nThe study aims to answer the following questions:\n\n* Can the AI-DSS support therapists in setting therapy parameters and adapting personalized robotic rehabilitation programs effectively?\n* Can AI-supported robotic rehabilitation improve upper limb function, activities of daily living (ADL), cognitive function, and quality of life compared with standard therapist-guided robotic rehabilitation?\n\nResearchers will compare two groups:\n\n* Robotic rehabilitation supported by the AI-DSS (CO-AIDER);\n* Robotic rehabilitation with parameters set by therapists (control group).\n\nParticipants will:\n\n* Receive robotic rehabilitation for the upper limb, either guided by the AI-DSS or by therapists;\n* Be monitored throughout the program, with therapy parameters adjusted according to their progress;\n* Complete assessments to evaluate changes in upper limb function, activities of daily living, cognitive function, and quality of life.\n\nThe study will also evaluate the usability and acceptability of the AI-supported robotic system as perceived by participants and clinical staff, and will include a cost-effectiveness analysis of the two interventions.",[58,59,60,27],"Stroke","Stroke Ischemic","Stroke Hemorrhagic",[58,62,63,64,65,66,67],"Upper limb rehabilitation","Artificial Intelligence","Robot-assisted therapy","AI-supported robotic system","AI-based decision support system","rehabilitation","NOT_YET_RECRUITING","2025-09-26",{"date":71,"type":36},"2025-09-30",{"date":73,"type":21},"2025-09",{"date":75,"type":21},"2026-12",{"name":77,"class":43},"Fondazione Don Carlo Gnocchi Onlus",10,{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":85,"eligibilityCriteria":86,"healthyVolunteers":87,"sex":16,"minAge":17,"maxAge":88,"enrollmentInfo":89,"targetDuration":91,"studyType":92,"phases":4,"briefSummary":93,"conditions":94,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":105,"locationsCount":4},"100580255","upper-limb-functional-index-100580255","NCT06834919","Upper Limb Functional Index","Translation, Cross-Cultural Adaptation, Validity and Reliability of Upper Limb Functional Index in Albanian Population","ULFI-A","Inclusion Criteria:\n\n* shoulder pain\n* arm pain\n* myofascial pain\n* muscular pain\n* trigger points\n* arthritis\n\nExclusion Criteria:\n\n* tumor\n* metabolic disease\n* neurologic conditions",true,"80 Years",{"count":90,"type":21},200,"7 Days","OBSERVATIONAL","To translate and validate the Upper Limb Functional Index into Albanian for use in the Albanian-speaking population.",[95,96,97,27],"Upper Limb Function","Upper Limb Pain","Upper Limb; Injury, Superficial, Multiple","2025-02-13",{"date":100,"type":36},"2025-02-19",{"date":102,"type":21},"2025-02-18",{"date":104,"type":21},"2025-03-15",{"name":106,"class":43},"Universidad Católica San Antonio de Murcia"]