[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"post-stroke-recovery\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:post-stroke-recovery":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,47],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100637837","combined-functional-electrical-and-transcranial-direct-current-stimulation-for-foot-drop-100637837",false,"NCT07592221","Combined Functional Electrical and Transcranial Direct Current Stimulation for Foot Drop","Combined Functional Electrical and Transcranial Direct Current Stimulation for Foot Drop: A Case Series","tDCS","Inclusion Criteria: To participate, you must be:\n\n* 18 years or older\n* Have had 1 or more strokes (\\> 6 months) affecting ankle dorsiflexion.\n* Discharged from all rehabilitative services.\n* Can walk independently with\u002Fwithout using an assistive device such as a cane without an ankle-foot orthosis (AFO) for 15 minutes.\n\nExclusion Criteria: You must not have:\n\n* An inability to repeat and understand 2-step commands.\n* Peripheral neuropathy\n* Damage to the skull or scalp, such as a fracture History of seizures or epilepsy Extremely high or low blood pressure or heart rate Chest pain or shortness of breath when you are resting Botox injections to your leg or foot in the last 4 months","ALL","18 Years",{"count":20,"type":21},30,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study aims to determine if combining the treatments of transcranial direct current stimulation (tDCS) and functional electrical stimulation (FES) will better help persons with stroke who have difficulty lifting their toes. As part of the treatment, subjects will receive electrical stimulation through pads on their scalp (similar to what one may have received in physical therapy previously to an arm or leg). This protocol is called transcranial direct current stimulation (tDCS). Subjects will also receive electrical stimulation through pads on their leg. This is called functional electrical stimulation (FES). During treatment sessions, subjects will also perform leg activity\u002Fstrengthening exercises. The aim is to evaluate whether combining FES and tDCS within a PT session would reduce foot drop as indicated by improvements in the amount of toe clearance and ankle motion persons with stroke.",[27,28,29],"Falls","Foot Drop","Post Stroke Recovery",[31,32,33],"transcranial direct current stimulation","functional electrical stimulation","minimum toe clearance","RECRUITING","2026-05-11",{"date":37,"type":38},"2026-05-18","ACTUAL",{"date":40,"type":21},"2026-06-01",{"date":42,"type":21},"2029-08-30",{"name":44,"class":45},"Saint Joseph's University, Philadelphia","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":22,"phases":57,"briefSummary":58,"conditions":59,"keywords":63,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":74,"lastUpdatePostDateStruct":75,"startDateStruct":77,"completionDateStruct":79,"leadSponsor":81,"locationsCount":5},"100584143","personalised-health-motor-and-cognitive-assistance-system-for-rehabilitation-phrase-100584143","NCT06885502","Personalised Health Motor and Cognitive Assistance System for RehAbilitation (PHRASE)","Personalised Health Motor and Cognitive Assistance System for RehAbilitation (PHRASE): A Randomized Clinical Trial","PHRASE-2024","Inclusion Criteria:\n\n* Patients presenting an ischemic or intracerebral haemorrhagic stroke, ≥ 3 months post-stroke.\n* Age \\> 18 years old\n* Moderate to mild proximal upper limb motor impairment Medical Research Council Scale (MRC \\>2).\n* ARAT: \\\u003C50, inclusive, to avoid ceiling effects while allowing room for improvement.\n* Able to sit on a chair or a wheelchair to interact with the RGS system.\n* Minimal experience with smartphone technology based on the clinician's opinion\n* Willing to participate and agree to comply with the trial scheme and procedures\n* Must sign an Informed Consent Form (ICF) indicating that they understand the purpose and the procedures of the study.\n\nExclusion Criteria:\n\n* Presence of a condition or abnormality that, in the opinion of the investigator, would compromise the safety of the patient or the quality of the data.\n* Severe cognitive capabilities that prevent the execution of the study, evaluated by the MoCA \\\u003C 19 or based on the clinician's opinion.\n* Pre-stroke history of upper limb motor disability.\n* Unable to use the RGS independently, according to the clinician's observations, and needing more support from a caregiver to use the RGS.",{"count":56,"type":21},70,[24],"This study is a multicentric randomized controlled trial evaluating the effectiveness of digital technology, specifically a smartphone with integrated VR-and AR-based intervention, for at-home rehabilitation after stroke. The study focuses on combined motor and cognitive training for patients in the late subacute and chronic phases post-stroke. The intervention is provided through the Rehabilitation Gaming System application RGSapp, a goal-oriented, first-person virtual reality (VR) and augmented reality (AR) mobile application for upper limb rehabilitation. A total of seventy participants will be randomly assigned (1:1 ratio) to either the RGSapp intervention or conventional therapy\u002Fstandard of care for six weeks. The primary outcome is motor function improvement (upper limb), assessed using the Action Research Arm Test (ARAT). Secondary outcomes include changes in cognitive function, depression, usability, adherence, validity of remote assessments, and healthcare costs.",[60,61,62,29],"Stroke","Stroke Rehabilitation","Chronic Stroke Patients",[60,64,65,66,67,68,69,70,71,72,73],"ARAT","Motor rehabilitation","Stroke rehabilitation","Telemedicine","Virtual Reality (VR)","Augmented Reality (AR)","Cognitive rehabilitation","Rehabilitation at home","eHealth technology","upper limbs","2025-12-31",{"date":76,"type":38},"2026-01-06",{"date":78,"type":38},"2025-02-21",{"date":80,"type":21},"2026-06-30",{"name":82,"class":83},"Eodyne Systems SL","INDUSTRY"]