[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100576558":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":21,"centralContacts":26,"locations":32,"responsibleParty":50,"collaborators":20,"id":52,"slug":53,"hasResults":54,"nctId":55,"briefTitle":56,"officialTitle":57,"acronym":58,"eligibilityCriteria":59,"healthyVolunteers":54,"sex":60,"minAge":61,"maxAge":20,"enrollmentInfo":62,"targetDuration":20,"studyType":65,"phases":66,"briefSummary":68,"conditions":69,"keywords":20,"overallStatus":35,"whyStopped":20,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":80},{"fullName":5,"class":6},"Medstar Health Research Institute","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"HandMate Use","EXPERIMENTAL","HandMate device fitted for a stroke participant.",[13],"Device: HandMate",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"DEVICE","HandMate","HandMate device is used for 20 hours in 4 weeks. Device is then used in the home for 3 months at discretion of participant.",[9],null,[22],{"name":23,"affiliation":24,"role":25},"Pete Lum, PhD","MedStar RI","PRINCIPAL_INVESTIGATOR",[27],{"name":28,"role":29,"phone":30,"phoneExt":20,"email":31},"Megan L Grainger","CONTACT","2028771464","megan.l.grainger@medstar.net",[33],{"facility":34,"status":35,"city":36,"state":37,"zip":38,"country":39,"countryCode":40,"cosmosGeoPoint":41,"geoPoint":46,"contacts":47},"MedStar National Rehabilitation Hospital","RECRUITING","Washington D.C.","District of Columbia","20010","United States","US",{"type":42,"coordinates":43},"Point",[44,45],-77.03637,38.89511,{"lat":45,"lon":44},[48],{"name":28,"role":29,"phone":49,"phoneExt":20,"email":31},"202-877-1464",{"type":51,"investigatorFullName":20,"investigatorTitle":20,"investigatorAffiliation":20,"oldNameTitle":20,"oldOrganization":20},"SPONSOR","100576558","hand-exoskeleton-training-study-100576558",false,"NCT06786858","Hand Exoskeleton Training Study","Home Training for Upper Limb Stroke Rehabilitation Using a Hand Exoskeleton","HandMATE","Inclusion Criteria:\n\n* Age of 21 or older\n* diagnosis of stroke more than 6 months prior confirmed from MRI or CT\n* voluntary hand activity (score of 1 or more, finger extension item, Fugl-Meyer Test)\n* adequate cognitive status\n* Impaired ability to open affected hand\n\nExclusion Criteria:\n\n* hemispatial neglect\n* severe sensory loss (2 or more on the sensory item, NIH Stroke Scale\u002FScore)\n* receiving or planning to receive antispasticity medications during enrollment into the study\n* less than full passive range of motion in finger joints\n* receiving physical or occupational therapy outside of study protocols\n* have excessive pain in any joint of the affected extremity that could limit ability to cooperate with the protocols","ALL","21 Years",{"count":63,"type":64},15,"ESTIMATED","INTERVENTIONAL",[67],"NA","The goal of this study is to evaluate the HandMATE device's effectiveness in the rehabilitation of stroke patients and asses if the HandMATE application is received well by stroke survivors.\n\nParticipants will use the HandMate device in clinic and in the home. They will also complete clinical upper extremity assessments.",[70],"Stroke","2025-01-15",{"date":73,"type":74},"2025-01-22","ACTUAL",{"date":76,"type":74},"2022-01-04",{"date":78,"type":64},"2025-01-31",{"name":5,"class":6},1]