[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100608470":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":24,"locations":34,"responsibleParty":55,"collaborators":58,"id":60,"slug":61,"hasResults":62,"nctId":63,"briefTitle":64,"officialTitle":65,"acronym":19,"eligibilityCriteria":66,"healthyVolunteers":62,"sex":67,"minAge":68,"maxAge":69,"enrollmentInfo":70,"targetDuration":19,"studyType":73,"phases":74,"briefSummary":76,"conditions":77,"keywords":79,"overallStatus":37,"whyStopped":19,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":94},{"fullName":5,"class":6},"McGill University","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"VR training","EXPERIMENTAL","Participants will engage in a 4-week VR intervention that comprises of 1-hour training sessions, 2 times\u002Fweek.",[13],"Other: Virtual Reality Training",[15],{"type":6,"name":16,"description":17,"armGroupLabels":18,"otherNames":19},"Virtual Reality Training","The VR intervention involves the intensive practice of community ambulation skills. The training sessions will be performed in a virtual environment. During the intervention, stroke participants will be invited to practice different dimensions of community ambulation, such as postural transitions, avoiding other pedestrians, dual-task walking, etc.",[9],null,[21],{"name":22,"affiliation":5,"role":23},"Anouk Lamontagne, PhD","PRINCIPAL_INVESTIGATOR",[25,30],{"name":22,"role":26,"phone":27,"phoneExt":28,"email":29},"CONTACT","450-688-9550","84168","anouk.lamontagne@mcgill.ca",{"name":31,"role":26,"phone":32,"phoneExt":19,"email":33},"Myriamn Villeneuve, Mec","514-216-1295","myriam.villeneuve@mail.mcgill.ca",[35],{"facility":36,"status":37,"city":38,"state":39,"zip":40,"country":41,"countryCode":42,"cosmosGeoPoint":43,"geoPoint":48,"contacts":49},"Jewish Rehabilitation Hospital","RECRUITING","Laval","Quebec","H7V1R2","Canada","CA",{"type":44,"coordinates":45},"Point",[46,47],-73.692,45.56995,{"lat":47,"lon":46},[50,51],{"name":22,"role":26,"phone":27,"phoneExt":28,"email":29},{"name":52,"role":26,"phone":27,"phoneExt":53,"email":54},"Vira Rose","84300","vrose_hjr@ssss.gouv.qc.ca",{"type":23,"investigatorFullName":56,"investigatorTitle":57,"investigatorAffiliation":5,"oldNameTitle":19,"oldOrganization":19},"Anouk Lamontagne","Associate Professor",[59],{"name":36,"class":6},"100608470","virtual-reality-for-post-stroke-gait-rehabilitation-100608470",false,"NCT07201974","Virtual Reality for Post-Stroke Gait Rehabilitation","iWalk in VR: Integration of Virtual Reality-based Locomotor Rehabilitation in Clinical Care","Inclusion Criteria:\n\nEligible patients with stroke referred by clinicians of the inpatient and outpatient stroke rehabilitation programs at the Jewish Rehabilitation Hospital (CISSS Laval) for mobility problems over a period of 6 months will be recruited. They will:\n\n* be aged between 40 and 74 years;\n* have normal\u002Fcorrected visual and auditory acuity present;\n* present a first-ever supratentorial unilateral stroke of 1-24 weeks duration;\n* present the ability to walk independently with\u002Fwithout walking aids for at least 1 min at a speed of 0.4-0.9 m\u002Fs;\n* present intact or mildly affected cognitive function (MoCA scores ≥ 22\u002F30);\n* present intact to moderately affected visual- perceptual function (positive scores on a max. of 3\u002F6 tasks on the Behavioural Inattention Test).\n\nExclusion Criteria:\n\n* Subjects with comorbidities interfering with walking\n* Subjects with comorbidities interfering with visual perception\n* Subjects without medical clearance for exercise","ALL","40 Years","84 Years",{"count":71,"type":72},40,"ESTIMATED","INTERVENTIONAL",[75],"NA","The goal of this clinical trial is to: (1) implement and test the feasibility of a new VR-ODT intervention offered as part of usual therapy time of patients with a sub-acute stoke; (2) explore the acceptability of the intervention from the perspective of clinicians and patients and; (3) implement measures to optimize the uptake and sustainability of the intervention within the clinical setting.\n\nParticipants will engage in a personalized VR-ODT training for 4 weeks (2X 1hr\u002Fweek) targeting six well-established community walking demands related to (1) walking speed and (2) distance; (3) postural transitions; (4) obstacle avoidance; (5) dual-task walking and; (6) a combination of demands 1-5. For each demand, patients will progress through levels of increasing difficulty according to personalized goals and success criteria.",[78],"Stroke",[80,81,82,83,84],"Rehabilitation","Intervention","Community Walking","Virtual Reality","Clinical care","2026-03-17",{"date":87,"type":88},"2026-03-20","ACTUAL",{"date":90,"type":88},"2026-02-01",{"date":92,"type":72},"2027-12",{"name":5,"class":6},1]