[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"stroke-subacute\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:stroke-subacute":200},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,8,0,[8,44,66,90,121,153,186,227],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100639947","virtual-reality-based-mindfulness-training-for-mental-health-after-stroke-100639947",false,"NCT07614373","Virtual Reality-based Mindfulness Training for Mental Health After Stroke","VITAL","Inclusion Criteria:\n\n* Ischemic or hemorrhagic stroke \\>6 months before inclusion\n* Anxiety-HAD score at inclusion \\>= 8\n\nExclusion Criteria:\n\n* Blindness\n* Deafness\n* Photo-sensitive epilepsy\n* unstable psychiatric condition","ALL","18 Years",{"count":19,"type":20},48,"ESTIMATED","INTERVENTIONAL",[23],"NA","Background: anxiety has a high prevalence in stroke patients and can dampen recovery of motor and cognitive impairment. Psychotropic medication can induce cognitive side effects, while psychotherapy and mindfulness-based stress reduction programs can be difficult to implement and are demanding for patients.\n\nAim: to evaluate the effect of a virtual reality (VR)-based medical device (HypnoVR®) on anxiety and stress reduction in patients with chronic stroke. Other outcomes, including depression, neurological fatigue and quality of life will be assessed.\n\nMethodology: a randomized controlled trial including patients who had an ischemic or hemorrhagic stroke (\\>6 months) and experience significant anxiety - Hospital Anxiety and Depression Scale (HADS) ≥ 8 for anxiety. Intervention includes 3 weekly HypnoVR® sessions for 3 weeks (total: 9), with clinical assessments at baseline, post-intervention (end of week 3) and at a 8-week follow-up. The sessions will be supervised by a research assistant and will take place in our outpatient clinic. Participants will be randomly assigned to either an immediate treatment group or a delayed treatment group (waiting list), the latter acting as both controls and active participants.\n\nPotential significance: VR-based therapeutic interventions are emerging as promising solutions to improve mental health but require solid scientific studies to assess their efficacy. This study provides a safe, non-invasive intervention for all included participants and could unveil its potential as an adjunctive therapy for mental health issues after stroke.",[26],"Stroke (Subacute)",[28,29,30],"stroke","virtual reality","anxiety","NOT_YET_RECRUITING","2026-05-20",{"date":34,"type":35},"2026-05-29","ACTUAL",{"date":37,"type":20},"2027-04-01",{"date":39,"type":20},"2029-03-31",{"name":41,"class":42},"Nicolas Nicastro","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":16,"minAge":51,"maxAge":4,"enrollmentInfo":52,"targetDuration":4,"studyType":21,"phases":54,"briefSummary":55,"conditions":56,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":4},"100634256","effect-of-dfm-on-quadriceps-spasticity-in-stroke-patients-100634256","NCT07537322","Effect of DFM on Quadriceps Spasticity in Stroke Patients","Effect of Deep Friction Massage on Quadriceps Spasticity in Patients With Sub-acute Stroke","Inclusion Criteria:\n\n* Age ≥ 40 years\n* Ischemic or hemorrhagic stroke diagnosis.\n* Subacute stage (1-6 months after stroke)\n* Quadriceps spasticity (Modified Ashworth Scale 1 or above)\n* Walking with or without assistive aids.\n* Stable health-wise and can be involved in rehabilitation.\n\nExclusion Criteria:\n\n* The participants were not allowed in case they had:\n* Severe mental failure (MMSE score under 24)\n* Lower limb musculoskeletal or other neurological disorders.\n* Contraindications to massage therapy (e.g. thrombosis, skin infection, fracture)\n* Weakened or no spasticity of the quadriceps.\n* Extreme medical instability inability to take part.","40 Years",{"count":53,"type":20},30,[23],"The goal of this clinical trial is to learn if deep friction massage works to reduce quadriceps muscle spasticity in adults with sub-acute Stroke. It will also learn about the effectiveness of this technique in improving lower limb motor function and mobility.\n\nThe main questions it aims to answer are:\n\n* Does deep friction massage reduce quadriceps spasticity in stroke patients as measured by the Modified Ashworth Scale?\n* Does deep friction massage improve lower limb motor recovery as measured by the Fugl-Meyer Assessment?\n* Does deep friction massage improve functional mobility as measured by the Timed Up and Go Test?\n\nResearchers will compare deep friction massage combined with conventional physiotherapy to conventional physiotherapy alone to see if deep friction massage improves spasticity and functional outcomes in patients with stroke.",[26],"2026-04-12",{"date":59,"type":35},"2026-04-17",{"date":61,"type":20},"2026-05-01",{"date":63,"type":20},"2027-12-30",{"name":65,"class":42},"Majmaah University",{"id":67,"slug":68,"hasResults":11,"nctId":69,"briefTitle":70,"officialTitle":71,"acronym":4,"eligibilityCriteria":72,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":73,"enrollmentInfo":74,"targetDuration":4,"studyType":21,"phases":76,"briefSummary":77,"conditions":78,"keywords":79,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":81,"lastUpdatePostDateStruct":82,"startDateStruct":84,"completionDateStruct":86,"leadSponsor":88,"locationsCount":43},"100631884","effect-of-immersive-virtual-reality-cognitive-rehabilitation-on-subacute-stroke-patients-a-pilot-study-100631884","NCT07506486","Effect of Immersive Virtual Reality Cognitive Rehabilitation on Subacute Stroke Patients (A Pilot Study)","Effect of Cognitive Rehabilitation Using Immersive Virtual Reality on Cognitive Function and Functional Activity of Subacute Stroke Patients: A Pilot Randomized Controlled Trial","Inclusion Criteria:\n\n* Male or female aged 40-59 years old\n* Stroke patient 2-4 months onset of stroke\n* Burnstorm stage V or above\n* First-time stroke that has been diagnosed by a neurologist with CT scan and\u002For MRI\n* Stroke risk factors and comorbidities are controlled with medication\n* Mild and moderate level of cognitive impairment based on MOCA and can use devices\n* Participants can grip and operate VR console with their hand\n* Participants can follow instructions and exercises\n* Participants were cooperative and willing to participate in the study by signing a consent form after receiving an explanation.\n\nExclusion Criteria:\n\n* Participants with severe cognitive impairment or aphasia struggle to understand instructions\n* Neglected patient\n* Participants with low vision unable to perceive content on screens\n* Participant with eyestrain characterized by blurring vision, dry eyes, foreign body sensation, itching watering, neck stiffness and backache\n* Severe musculoskeletal disorders causing problem in standing and following instruction","59 Years",{"count":75,"type":20},22,[23],"This pilot randomized controlled trial aims to evaluate the effectiveness of cognitive rehabilitation using an immersive Virtual Reality (VR) system compared to conventional paper-and-pencil cognitive training in subacute stroke patients. A total of 22 participants will be randomly assigned to either the VR intervention group (n=11) or the conventional control group (n=11). The study will measure changes in cognitive function and functional independence",[26],[80],"cognitive impairment","2026-03-31",{"date":83,"type":35},"2026-04-06",{"date":85,"type":20},"2026-04-15",{"date":87,"type":20},"2026-09-30",{"name":89,"class":42},"Universitas Padjadjaran",{"id":91,"slug":92,"hasResults":11,"nctId":93,"briefTitle":94,"officialTitle":95,"acronym":4,"eligibilityCriteria":96,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":97,"targetDuration":4,"studyType":21,"phases":99,"briefSummary":101,"conditions":102,"keywords":106,"overallStatus":111,"whyStopped":4,"lastUpdateSubmitDate":112,"lastUpdatePostDateStruct":113,"startDateStruct":115,"completionDateStruct":117,"leadSponsor":119,"locationsCount":43},"100629016","phase-1-phase-i-split-belt-treadmill-dosing-for-subacute-stroke-100629016","NCT07469163","Phase I Split-Belt Treadmill Dosing for Subacute Stroke","NeuroRecoVR: Phase I Split-Belt Treadmill Dosing for Subacute Stroke","Inclusion Criteria:\n\n* Ischemic or hemorrhagic stroke survivors\n* First stroke\n* Over 18 years old\n* Between one week and three months post-stroke\n* can understand task instructions.\n\nExclusion Criteria:\n\n* History of significant neurological diseases (e.g. Multiple Sclerosis, Parkinson's disease)\n* Orthopedic issues in lower extremities (e.g. severe knee Osteoarthritis)\n* Excessive pain preventing participants from participating in treadmill-based activities\n* Cerebellar stroke\n* Body weight more than 560 lbs (this exceeds the weight limit of the support harness)",{"count":98,"type":20},72,[100],"PHASE1","After experiencing a stroke, many individuals encounter difficulties with walking and balance, which can significantly impact their independence. Recent studies have indicated that split-belt treadmill (SBT) training is effective for improving gait metrics, including walking speed and step length asymmetry. The SBT allows each leg to move at different speeds, which has been shown to help chronic stroke survivors learn to walk more symmetrically. However, there is limited knowledge about the dose participants should receive and the safety of SBT training in the early stages of recovery, which is a crucial period for rehabilitation. To address this gap, we are evaluating an innovative SBT with virtual reality (VR) features at the Foothills Medical Center. Our objective is to conduct a study to determine the amount of SBT training patients can tolerate in a day. In this study, stroke survivors will engage in a series of walking exercises on the SBT. We will escalate the duration of SBT walking until participants reach a point where they can no longer continue due to dose-limiting criteria such as fatigue or discomfort. The findings from this initial phase will guide future larger trials to explore the effectiveness of this training method. Ultimately, we aspire to improve rehabilitation strategies for stroke survivors, assisting them in regaining mobility and enhancing their quality of life more effectively.",[103,104,26,105],"Subacute Stroke","Stroke","Stroke Gait Rehabilitation",[28,107,108,109,110],"subacute stroke","split belt treadmill","gait rehabilitation","stroke recovery","RECRUITING","2026-03-09",{"date":114,"type":35},"2026-03-13",{"date":116,"type":35},"2026-03-01",{"date":118,"type":20},"2026-08-31",{"name":120,"class":42},"University of Calgary",{"id":122,"slug":123,"hasResults":11,"nctId":124,"briefTitle":125,"officialTitle":125,"acronym":126,"eligibilityCriteria":127,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":128,"enrollmentInfo":129,"targetDuration":4,"studyType":21,"phases":131,"briefSummary":132,"conditions":133,"keywords":134,"overallStatus":111,"whyStopped":4,"lastUpdateSubmitDate":143,"lastUpdatePostDateStruct":144,"startDateStruct":146,"completionDateStruct":148,"leadSponsor":150,"locationsCount":152},"100627430","comparative-effects-of-functional-electrical-stimulation-and-mirror-therapy-for-foot-clearance-among-patients-with-sub-acute-stroke-100627430","NCT07448532","Comparative Effects of Functional Electrical Stimulation and Mirror Therapy for Foot Clearance Among Patients With Sub-acute Stroke","FES MT CVA","Inclusion Criteria:\n\n* Patient aged 18-85 years of age, who experienced stroke within ≤6 months.\n* The Fugl-Meyer motor assessment of lower extremity (FMA-LE) was conducted by physiotherapist in the hospital, and score required to be ≥ 20 points.\n* Participants possessed healthy nerves, neuromuscular junctions, muscles tissues, and a sufficient range of motion in dorsiflexor and plantarflexion.\n* The subjects could walk independently on a treadmill for at least 2 min without without experiencing adverse reaction to FES.\n* Patients who received more 24 scores on Mini Mental State Exam and could comprehend and follow the information researcher provides.\n* No orthopedic diseases in upper and lower extremities.\n* Patients with functional ambulation classification (FAC) score of 3 or 4 were included (FAC is a scale of 0-5, where 3 indicates supervision or standby guarding and 4 indicates independent on level surfaces.\n* Patients with inadequate ankle dorsiflexion during the swing phase of gait.\n* Patients with adequate minimal stability at the ankle during stance with stimulation.\n\nExclusion Criteria:\n\n* Patients with cardiac pacemaker, those with skin lesions, who could not be treated due to spasticity within the last three months, and vestibular and cerebellar lesions or deaf- blindness were excluded.\n* Patients with past or current epilepsy, uncontrolled seizure disorder, mental disorders and all neurological disorders except stroke.\n* Patients with severe edema of lower extremities or patients of vascular disorders like deep vein thrombosis or thromboembolisms and severe atheroscelerosis of lower extremities.\n* Subjects with any musculoskeletal dysfunction that would potentially affect gait and causes risk of falls.\n* We excluded patients with pregnancy, plantar flexion contracture, and severe hemi-neglect.\n* Subjects with hip or knee prostheses made of metal on the lower limb were excluded.","85 Years",{"count":130,"type":20},38,[23],"This study aims to evaluate the effectiveness of two rehabilitation techniques- Functional Electrical Stimulation (FES) and Mirror Therapy (MT)-in improving motor recovery among stroke survivors. Stroke often results in long-term impairments, particularly in foot clearance, which is critical for daily activities. Although current rehabilitation strategies help, more effective solutions are needed to enhance recovery. Participants, aged 18- 85 years old with subacute stroke and foot clearance impairments, will be randomized into two groups: Group A will receive functional electrical stimulation (FES) with routine physical therapy; and Group B will receive mirror therapy (MT) with routine physical therapy. The interventions will take place three times a week for 4 weeks, and participants will undergo motor function assessments, including the Fugl-Meyer Assessment and Functional Independence Measure, before and after the intervention. The study will compare the effects of each intervention on motor recovery, specifically focusing on tibialis anterior function and motor control. The findings could lead to improved rehabilitation protocols, offering stroke survivors better therapeutic options and enhancing their quality of life.",[26],[135,136,137,138,139,140,141,142],"Fugl-Meyer Assessment","Functional Independence Measure","Lower limb rehabilitation","Stroke (subacute)","Foot Clearance","Neuromuscular Rehabilition","Mirror therapy (MT)","Functional Electrical Stimulation (FES)","2026-02-26",{"date":145,"type":35},"2026-03-04",{"date":147,"type":35},"2026-01-22",{"date":149,"type":20},"2026-06-27",{"name":151,"class":42},"Lahore University of Biological and Applied Sciences",2,{"id":154,"slug":155,"hasResults":11,"nctId":156,"briefTitle":157,"officialTitle":158,"acronym":159,"eligibilityCriteria":160,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":161,"targetDuration":4,"studyType":21,"phases":163,"briefSummary":164,"conditions":165,"keywords":167,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":177,"lastUpdatePostDateStruct":178,"startDateStruct":180,"completionDateStruct":182,"leadSponsor":184,"locationsCount":43},"100572035","aggregated-system-of-sensors-and-multimedia-monitors-technology-for-innovation-and-personalization-of-rehabilitation-care-roommate-100572035","NCT06728020","AggRegated System Of sensOrs and Multimedia Monitors: Technology for innovAtion and personalizaTion of rEhabilitation Care. (ROOMMATE)","ROOMMATE - AggRegated System Of sensOrs and Multimedia Monitors: Technology for innovAtion and personalizaTion of rEhabilitation Care.","ROOMMATE","Inclusion Criteria:\n\n* outcome of ischemic or hemorrhagic stroke in subacute phase (\\\u003C 3 months after the event)\n* willingness to participate in the project, with informed consent signed by the subject or, when necessary, by the support administrator.\n\nExclusion Criteria:\n\n* severe visual and\u002For auditory impairments that cannot be corrected\n* severe cognitive and\u002For speech impairments that interfere with the ability to use the HKK system and the SensoMode accessory independently and\u002For in the\n* absence of a caregiver who can assist the patient in using the system;\n* skin lesions that prevent wearing the inertial sensors;\n* presence of signs of clinical instability, defined by a score greater than zero on the Clinical Instability Scale (SIC).",{"count":162,"type":20},200,[23],"The aim of this clinical trial is to assess whether the ROOMMATE system can effectively support the rehabilitation of adults recovering from subacute strokes. The study will be conducted at the neuromotor rehabilitation inpatient clinics of IRCCS Fondazione Don Carlo Gnocchi in Florence, Italy, and the rehabilitation inpatient unit of Elias University Emergency Hospital in Bucharest, Romania.\n\nPrimary Objectives:\n\n-To assess the effects on functional recovery in subacute stroke survivors of a technological rehabilitation station placed at patients' bedsides, combined with dedicated coaching provided to all users (patients, informal caregivers, and formal caregivers).\n\nSecondary Objectives:\n\n* Evaluation of the effects of the experimental treatment on patient satisfaction, upper limb motor skills, manual dexterity, global cognitive functioning, anxiety, and depression.\n* Assessment of user experience, acceptance, and usability of the technology by patients and caregivers.\n* Evaluation of social impact using the Social Return on Investment (SROI) ratio of the experimental treatment.\n\nParticipants randomized into one of the experimental groups, in addition to receiving conventional care, will use the ROOMMATE system during their hospitalization. The system will be made available to patients and will be free for them to use at their discretion.\n\nThe station will include:\n\nMultimedia monitors (Khymeia home kit): These will deliver cognitive and motor serious games, educational and rehabilitative content, as well as infotainment specifically developed by the clinical partners of the project.\n\nAn inertial sensor kit: This integrates with the monitors to guide users through virtual reality environments.",[103,166],"Stroke; Subacute",[107,168,169,170,171,172,173,174,175,176],"Neurorehabilitation","Assistive\u002Frehabilitation robotics","Digital health","Continuum of care","People-centered care","Accessible care","Innovation adoption","cmRCT","Enriched environment","2025-03-18",{"date":179,"type":35},"2025-03-21",{"date":181,"type":20},"2025-04",{"date":183,"type":20},"2026-05",{"name":185,"class":42},"Francesca Cecchi",{"id":187,"slug":188,"hasResults":11,"nctId":189,"briefTitle":190,"officialTitle":190,"acronym":191,"eligibilityCriteria":192,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":193,"targetDuration":4,"studyType":21,"phases":195,"briefSummary":196,"conditions":197,"keywords":207,"overallStatus":111,"whyStopped":4,"lastUpdateSubmitDate":216,"lastUpdatePostDateStruct":217,"startDateStruct":219,"completionDateStruct":221,"leadSponsor":223,"locationsCount":226},"100524306","effects-of-atalante-exoskeleton-on-gait-recovery-in-non--or-poorly-ambulatory-patients-with-hemiparesis-in-the-acutesubacute-phase-month-1-to-4-100524306","NCT06107010","Effects of Atalante Exoskeleton on Gait Recovery in Non- or Poorly Ambulatory Patients With Hemiparesis in the Acute\u002FSubacute Phase (Month 1 to 4)","EarlyExo","Inclusion Criteria:\n\n* \\>18 years old\n* First clinically significant disability due to stroke\n* Hemiparesis in acute-subacute phase (1 to 4 months since lesion) due to a stroke\n* Functional Ambulation Category score (FAC) \\\u003C2\n* Patient with health insurance\n* Informed and willing to sign an informed consent form approved by the Ethics Committee. For clarity, if a motor impairment prevents the subject from signing by himself, he\u002Fshe can still be included if the signature can be done by an impartial witness.\n\nExclusion Criteria:\n\n* Muscle overactivity in hip adductors, hamstrings, quadriceps and plantar flexors, which interferes with exoskeleton use, based on clinician investigator's opinion\n* Recent fracture (\\\u003C 3 months) or any therapy inducing secondary osteoporosis\n* Excessive joint mechanical pain in the lower limbs based on clinician investigator's opinion\n* Pressure sore grade I or more over contact zones with Atalante system, according to the International Pressure Ulcer Classification System NPUAP - EPUA\n* Medical contra-indication to medium intensity physical strain\n* Orthostatic hypotension (loss of \\> 20 mmHg systolic BP after 3 minutes in standing position)\n* Uncontrolled seizures\n* Morphological contra-indications to the use of Atalante (as per user's manual)\n* Pregnant woman\n* Adults who lack the capacity to provide informed consent, and all those persons deprived of their liberty in prisons or other places of detention\n* Concurrent participation in another interventional trial",{"count":194,"type":20},66,[23],"The present clinical investigation - EarlyExo, is an interventional, international, multicentric, prospective, single-blinded randomized controlled trial.\n\nThis clinical investigation is designed to test the hypothesis that early and intense introduction of walking sessions assisted by the Atalante exoskeleton, in a sample of hemiparetic patients with still non or poor ambulatory capacities (FAC 0 or 1) between one- and four-months post stroke, would result in a better recovery of functional walking compared to a control group only receiving conventional therapy. Improved recovery will be measured through the proportion of patients reaching a FAC score of 4 or higher at the end of the intervention period. The tested hypothesis is that this proportion will be higher in the Exo group.\n\nThe duration of the intervention period in both groups is 6 weeks.\n\n* For the Exo group: 3 sessions per week (i.e., 18 one-hour sessions) with the Atalante device and 2 sessions per week (i.e., 12 one-hour sessions) of conventional therapy.\n* For the Control group: 5 sessions per week of conventional therapy (i.e., 30 one-hour sessions).\n\nThe study will include 66 patients (33 in each arm) and takes place in two French centers, two German centers and one Spanish center.",[198,199,200,201,202,203,204,205,206],"Stroke, Acute","Stroke, Ischemic","Stroke, Subacute","Stroke Hemorrhagic","Cerebrovascular Disorders","Cerebrovascular Accident","Hemiparesis","Hemiparesis;Poststroke\u002FCVA","Hemiparesis\u002FHemiplegia (One Sided Weakness\u002FParalysis)",[208,209,210,211,104,212,213,214,215],"Robotics","Rehabilitation","Powered Exoskeleton","Walking recovery","Acute stroke","Subacute stroke","Functional Ambulation Category","Randomized controlled study","2025-01-30",{"date":218,"type":35},"2025-02-04",{"date":220,"type":35},"2023-06-12",{"date":222,"type":20},"2026-02-28",{"name":224,"class":225},"Wandercraft","INDUSTRY",5,{"id":228,"slug":229,"hasResults":11,"nctId":230,"briefTitle":231,"officialTitle":232,"acronym":233,"eligibilityCriteria":234,"healthyVolunteers":235,"sex":16,"minAge":17,"maxAge":236,"enrollmentInfo":237,"targetDuration":4,"studyType":21,"phases":239,"briefSummary":240,"conditions":241,"keywords":242,"overallStatus":111,"whyStopped":4,"lastUpdateSubmitDate":245,"lastUpdatePostDateStruct":246,"startDateStruct":248,"completionDateStruct":250,"leadSponsor":252,"locationsCount":152},"100497715","bimanual-motor-skill-learning-in-acute-stroke-100497715","NCT05760846","Bimanual Motor Skill Learning in Acute Stroke","Exploring the Neural Substrates of Proximal and Distal Bimanual Motor Skill Learning Through Robotics and Multimodal Brain Imaging","MLAS4","ACUTE STROKE PATIENTS:\n\nInclusion Criteria:\n\n* acute stroke (\\\u003C 21 days)\n* aged 18-90 years\n* with a demonstrated stroke (ischemic or hemorrhagic) lesion on brain imaging\n\nExclusion Criteria:\n\n* \" classical \" contre-indication to MRI (non-MR-compatible pacemaker, pregnancy, non-MR-compatible implanted devices, claustrophobia, etc ...)\n* difficulty in understanding or executing commands\n* drug\u002Falcohol abuse\n* severe aphasia \u002F cognitive deficits interfering with study\n* inability to complete the tasks (i.e. full paralysis of the arm)\n* multiple strokes \u002F dementia \u002F psychiatric condition\n\nHEALTHY INDIVIDUALS:\n\nInclusion Criteria:\n\n• 18-90 years\n\nExclusion Criteria:\n\n* medical history with a previous stroke \u002F relevant neurological deficit\n* drug\u002Falcohol abuse\n* psychiatric condition\u002F dementia",true,"90 Years",{"count":238,"type":20},160,[23],"The subacute phase of stroke provides a window into how a lesion perturbs sensorimotor functions prior to reorganisation driven by plasticity and neurorehabilitation. The recovery from motor impairment has been extensively studied, but it is currently unknown whether motor skill learning (MSkL) is enhanced or impaired during acute stroke, especially bimanual motor skill learning (bim-MSkL), which likely requires more motor-attentional-cognitive resources than unimanual MSkL.\n\nThe goals of this project are: to determine the neural substrates critical to achieve proximal and distal bimanual motor skill learning (bim-MSkL) by specifying whether (sub)acute stroke to different brain areas (cortical and subcortical) induce specific deficits in bimanual and\u002For distal bim-MSkL, which behavioral components are involved in bim-MSkL, and whether damage to the motor, sensory and inter-hemispheric pathways specifically impairs proximal and\u002For distal bim-MSkL.",[198,200],[243,244,212,209,213],"Motor Skill Learning","Upper limb","2024-12-10",{"date":247,"type":35},"2024-12-16",{"date":249,"type":35},"2023-04-17",{"date":251,"type":20},"2028-10",{"name":253,"class":42},"University Hospital of Mont-Godinne"]