[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100495258":3},{"organization":4,"armGroups":7,"interventions":25,"overallOfficials":35,"centralContacts":40,"locations":45,"responsibleParty":60,"collaborators":62,"id":64,"slug":65,"hasResults":66,"nctId":67,"briefTitle":68,"officialTitle":68,"acronym":24,"eligibilityCriteria":69,"healthyVolunteers":66,"sex":70,"minAge":71,"maxAge":24,"enrollmentInfo":72,"targetDuration":24,"studyType":75,"phases":76,"briefSummary":78,"conditions":79,"keywords":82,"overallStatus":47,"whyStopped":24,"lastUpdateSubmitDate":88,"lastUpdatePostDateStruct":89,"startDateStruct":92,"completionDateStruct":94,"leadSponsor":96,"locationsCount":97},{"fullName":5,"class":6},"Mindmaze SA","INDUSTRY",[8,14,20],{"label":9,"type":10,"description":11,"interventionNames":12},"Rehabilitation intervention group","EXPERIMENTAL","Each participant of the experimental group will undergo an initial cognitive screening (pre-training) and, in addition to their standard of care, they will have 20 additional sessions with the experimental rehabilitation program. Post-treatment cognitive screening will be completed at the end of the program, then 3-4 and 6-12 months later.",[13],"Other: Immersive virtual reality gamified cognitive activities",{"label":15,"type":16,"description":17,"interventionNames":18},"Dose-match control group","ACTIVE_COMPARATOR","Each participant of the experimental group will undergo an initial cognitive screening (pre-training) and, in addition to their standard of care, they will have 20 additional sessions of neuropsychological standard sessions. Post-treatment cognitive screening will be completed at the end of the program, then 3-4 and 6-12 months later.",[19],"Other: Double neuropsychological standard activities",{"label":21,"type":22,"description":23,"interventionNames":24},"Retrospective standard of care group","NO_INTERVENTION","Each participant of the retrospective group will be included retrospectively if they were hospitalized in the study's sites between 2012 and 2022, and followed standard neuropsychological rehabilitation of attention.",null,[26,31],{"type":27,"name":28,"description":29,"armGroupLabels":30,"otherNames":24},"OTHER","Immersive virtual reality gamified cognitive activities","This intervention will include 20 sessions of training with the experimental rehabilitation program using immersive VR cognitive gamified activities, in addition to the standard of care.",[9],{"type":27,"name":32,"description":33,"armGroupLabels":34,"otherNames":24},"Double neuropsychological standard activities","This intervention will include 20 sessions of training using a standard neuropsychological rehabilitation program, in addition to the standard of care.",[15],[36],{"name":37,"affiliation":38,"role":39},"Sonia Crottaz-Herbette","University of Lausanne Hospitals","PRINCIPAL_INVESTIGATOR",[41],{"name":37,"role":42,"phone":43,"phoneExt":24,"email":44},"CONTACT","+41213149348","sonia.crottaz-herbette@chuv.ch",[46],{"facility":38,"status":47,"city":48,"state":24,"zip":49,"country":50,"countryCode":51,"cosmosGeoPoint":52,"geoPoint":57,"contacts":58},"RECRUITING","Lausanne","1015","Switzerland","CH",{"type":53,"coordinates":54},"Point",[55,56],6.63282,46.516,{"lat":56,"lon":55},[59],{"name":37,"role":42,"phone":43,"phoneExt":24,"email":44},{"type":61,"investigatorFullName":24,"investigatorTitle":24,"investigatorAffiliation":24,"oldNameTitle":24,"oldOrganization":24},"SPONSOR",[63],{"name":38,"class":27},"100495258","virtual-reality-exercises-for-alleviating-attention-deficits-in-patients-with-acquired-brain-injury-100495258",false,"NCT05728840","Virtual-reality Exercises for Alleviating Attention Deficits in Patients With Acquired Brain Injury","Inclusion Criteria:\n\n* Time from stroke onset \\\u003C 1 month\n* Objective pathological performance on at least one standardized test or subtest on attention during standard neuropsychological evaluation\n* Brain injury documented by routine neuroradiological examination (computed tomography or magnetic resonance imaging scan)\n* Able to give informed consent as documented by signature\n* Age \\>= 18 years old\n\nExclusion Criteria:\n\n* Epilepsy\n* Inability or contraindications to undergo the investigated intervention\n* Major psychiatric co-morbidity\n* Major neurocognitive deficits (e.g. dementia)\n* Incapacity to discriminate colors\n* General cognitive state preventing to understand and perform the tasks\n* Decision to not be informed of incidental findings","ALL","18 Years",{"count":73,"type":74},135,"ESTIMATED","INTERVENTIONAL",[77],"NA","Stroke is the leading cause of long-term disability with an increasing incidence, especially in young adults. Among the cognitive difficulties following brain damage, deficits in attention are frequent and pervasive, affecting between 46% and 92% of stroke survivors. The current project targets patients with acquired brain injury, including stroke, traumatic brain injury, and brain tumor. The main objective of this study is to evaluate the use and the efficacy of a training program targeting attention and executive function difficulties, using gamified and digitized versions in virtual reality of standard cognitive exercises for patients with brain lesions.",[80,81],"Stroke","Attention Disorder",[83,84,85,86,87],"stroke","attention","executive functions","virtual reality","neurorehabilitation","2026-02-13",{"date":90,"type":91},"2026-02-17","ACTUAL",{"date":93,"type":91},"2023-02-15",{"date":95,"type":74},"2026-07-31",{"name":5,"class":6},1]