[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100053736":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":24,"locations":29,"responsibleParty":46,"collaborators":10,"id":48,"slug":49,"hasResults":50,"nctId":51,"briefTitle":52,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":50,"sex":55,"minAge":56,"maxAge":10,"enrollmentInfo":57,"targetDuration":10,"studyType":60,"phases":10,"briefSummary":61,"conditions":62,"keywords":64,"overallStatus":32,"whyStopped":10,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":78},{"fullName":5,"class":6},"Azienda Unita Sanitaria Locale di Piacenza","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"PwS",null,"Adult People with Stroke (PwS) with Upper Limb (UL) motor function impairment",[13],"Device: Technology-based UL rehabilitation",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":10},"DEVICE","Technology-based UL rehabilitation","Participants will receive conventional treatments, including neuromotor, occupational therapy, speech therapy and\u002For neuropsychology treatments, as clinically indicated. In addition, they will undergo a personalized and specific UL technology-based rehabilitation programme, delivered 3 times per week, for a total of 12 - 15 sessions. Each session will last 1 hour and will be conducted in a 1:1 format (physiotherapist : participant). Data on rehabilitation dosage will be collected, including the total number of hours of rehabilitation received. Physiotherapists who will have in charge participant, will compiled a treatment diary for each technology session in which they will record: number of session, total hour of technology-based treatments, type of device used and any adverse events.",[9],[21],{"name":22,"affiliation":5,"role":23},"Gianfranco Lamberti, MD","PRINCIPAL_INVESTIGATOR",[25],{"name":22,"role":26,"phone":27,"phoneExt":10,"email":28},"CONTACT","+39 0523 404656","g.lamberti2@ausl.pc.it",[30],{"facility":31,"status":32,"city":33,"state":34,"zip":35,"country":36,"countryCode":37,"cosmosGeoPoint":38,"geoPoint":43,"contacts":44},"Fiorenzuola d'Arda Hospital - AUSL Piacenza","RECRUITING","Fiorenzuola d'Arda","Piacenza","29017","Italy","IT",{"type":39,"coordinates":40},"Point",[41,42],9.91329,44.92435,{"lat":42,"lon":41},[45],{"name":22,"role":26,"phone":27,"phoneExt":10,"email":28},{"type":23,"investigatorFullName":22,"investigatorTitle":47,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"MD","100053736","effects-of-using-advanced-neurorehabilitation-technologies-in-upper-limb-motor-function-and-capacity-recovery-in-people-with-stroke-100053736",false,"NCT07698405","Effects of Using Advanced NEUROrehabilitation TECHnologies in Upper Limb Motor Function and Capacity Recovery in People With Stroke","NEURO-TECH","Inclusion Criteria:\n\n* Age ≥ 18 years;\n* First-ever unilateral ischemic or hemorrhagic stroke;\n* Presence of upper limb motor impairment;\n* Modified Ashworth Scale (MAS) \\\u003C 3;\n* Montreal Cognitive Assessment (MoCA) \\> 24;\n* Medically stable and able to participate in an intensive rehabilitation programme;\n* Ability to understand and follow study procedures;\n* Written informed consent.\n\nExclusion Criteria:\n\n* Diagnosis of severe aphasia, based on medical records, preventing participation;\n* Bilateral hemisphere lesions;\n* Severe and unstable medical conditions (e.g. untreated seizure, heart failure) that preclude participation in rehabilitation;\n* Other neurological and\u002For psychiatric diseases;\n* Recent and unstabilized upper limb fracture.","ALL","18 Years",{"count":58,"type":59},25,"ESTIMATED","OBSERVATIONAL","This study aims to evaluate the effect of a personalized technology-based rehabilitative intervention on Upper Limb (UL) motor function and capacity recovery in People with Stroke (PwS). The study is single-cohort study in which eligible participants will undergo baseline and follow-up clinical and instrumental assessments over a 4-5 week period.\n\nThe intervention consists of a personalized and specific upper limb technology-based rehabilitation programme delivered three times per week for a total of 12-15 sessions. Each session lasts approximately one hour and is integrated with conventional rehabilitation treatments.\n\nPrimary outcomes include Fugl-Meyer Assessment for Upper Extremity (FMA-UE) and Action Research Arm Test (ARAT). Secondary outcomes include instrumental assessment of active range of motion and grip strength.",[63],"Stroke",[63,65,66,67,68],"Technology-Assisted Rehabilitation","Robotics","Virtual Reality","Motor Recovery","2026-07-07",{"date":71,"type":72},"2026-07-13","ACTUAL",{"date":74,"type":72},"2026-06-15",{"date":76,"type":59},"2027-08",{"name":5,"class":6},1]