[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"cerebral-vascular-accident\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:cerebral-vascular-accident":33},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,49],{"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":21,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":34,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100310212","stroke-recovery-initiative---registry-for-stroke-research-studies-100310212",false,"NCT03318432","Stroke Recovery Initiative - Registry for Stroke Research Studies","Stroke Recovery Initiative - Stroke Registry","* 18 years of age or older\n* Have suffered a stroke\n* Have ongoing symptoms as a result of the stroke","ALL","18 Years",{"count":19,"type":20},60000,"ESTIMATED","5 Years","OBSERVATIONAL","The Stroke Recovery Initiative is a nation-wide participant recruitment registry that connects people who have had a stroke with researchers who are working to develop new approaches to improve recovery after stroke.",[25,26,27,28,29,30,31,32,33],"Stroke","Acute Stroke","Ischemic Stroke","Hemorrhagic Stroke","Subarachnoid Hemorrhage","Cerebral Ischemia","Cerebral Infarction","Cerebral Stroke","Cerebral Vascular Accident",[25,26,27,28,30,31,32,33,35],"Stroke Recovery","RECRUITING","2025-09-26",{"date":39,"type":40},"2025-10-02","ACTUAL",{"date":42,"type":40},"2013-02-09",{"date":44,"type":20},"2028-09",{"name":46,"class":47},"University of California, San Francisco","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":56,"sex":16,"minAge":57,"maxAge":58,"enrollmentInfo":59,"targetDuration":4,"studyType":61,"phases":62,"briefSummary":64,"conditions":65,"keywords":66,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":48},"100566473","safety-and-feasibility-of-an-exonet-for-supination-assistance-for-stroke-survivors-100566473","NCT06655636","Safety and Feasibility of an ExoNET for Supination Assistance for Stroke Survivors","Assisting Stroke Survivors With Engineering Technology (ASSET): Design Project D3: Exoskeletal Networks for Forearm Supination","Inclusion Criteria:\n\n1. Between the ages of 40-70 (to reduce confounding effects of aging on muscle, movement accuracy and proprioception)\n2. Have sustained a single, unilateral stroke at least 8 months prior to enrollment\n3. Severe to moderate upper extremity impairment (ARAT score 0-30)\n4. Ability to move their elbow and wrist when supported against gravity\n5. Cortical stroke with hemiparesis, tactile sensation\n6. Available medical records about lesion locations indicating the stroke was caused by a middle cerebral artery ischemic infarct\n\nExclusion Criteria:\n\n1. Bilateral paresis\n2. Diffuse\u002Fmultiple lesion sites or multiple stroke events\n3. Hemispatial neglect or visual field cut that prevent visual feedback\n4. Shoulder pain and\u002For articular rigidity on the upper limb joint\n5. Severe sensory deficits indicated by the Two-Point Discrimination Test\n6. Botox injection to the affected upper extremity within the previous 4 months\n7. Aphasia, cognitive impairment, or affective dysfunction that would influence the ability to consent, perform the experiment, or follow commands\n8. Concurrent participation in upper extremity rehabilitation either as part of a research intervention protocol or a prescribed therapy\n9. Other neurological issues\n10. Meet any of the contraindications to Delsys Trigno Sensors:\n\n    * Implanted with electronic devices of any kind, including cardiac pace-makers or similar assistive devices, electronic induction pumps, and implanted stimulators\n    * Irritated skin or open wounds\n    * Silver allergy",true,"40 Years","70 Years",{"count":60,"type":20},30,"INTERVENTIONAL",[63],"NA","The purpose of this study is to evaluate the safety, feasibility, and efficacy of an exoskeletal network of passive, multi-joint springs for forearm supination. Also known as the forearm ExoNET, the device is a passive, robotic device that will properly assist forearm supination in the post-stroke adult population.",[25,33],[67,68,25],"Upper Extremity","Rehabilitation","2025-01-07",{"date":71,"type":40},"2025-01-09",{"date":73,"type":40},"2024-12-04",{"date":75,"type":20},"2025-12",{"name":77,"class":47},"Shirley Ryan AbilityLab"]