[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100573662":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":25,"centralContacts":26,"locations":32,"responsibleParty":50,"collaborators":54,"id":60,"slug":61,"hasResults":62,"nctId":63,"briefTitle":64,"officialTitle":65,"acronym":66,"eligibilityCriteria":67,"healthyVolunteers":62,"sex":68,"minAge":69,"maxAge":25,"enrollmentInfo":70,"targetDuration":25,"studyType":73,"phases":74,"briefSummary":76,"conditions":77,"keywords":79,"overallStatus":35,"whyStopped":25,"lastUpdateSubmitDate":86,"lastUpdatePostDateStruct":87,"startDateStruct":90,"completionDateStruct":92,"leadSponsor":94,"locationsCount":95},{"fullName":5,"class":6},"Erasmus Medical Center","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Early cognitive training, followed by standard care","EXPERIMENTAL","Rehacom, standard care",[13],"Device: Rehacom",{"label":15,"type":16,"description":17,"interventionNames":18},"Standard care, followed by cognitive training","ACTIVE_COMPARATOR","Standard care, Rehacom",[13],[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":25},"DEVICE","Rehacom","Home-based cognitive training program",[9,15],null,[27],{"name":28,"role":29,"phone":30,"phoneExt":25,"email":31},"Majanka H Heijenbrok-Kal, PhD","CONTACT","+31 6 28129140","m.heijenbrok@erasmusmc.nl",[33],{"facility":34,"status":35,"city":36,"state":37,"zip":38,"country":39,"countryCode":40,"cosmosGeoPoint":41,"geoPoint":46,"contacts":47},"Rijndam Rehabilitation","RECRUITING","Rotterdam","South Holland","3015LJ","Netherlands","NL",{"type":42,"coordinates":43},"Point",[44,45],4.47917,51.9225,{"lat":45,"lon":44},[48],{"name":28,"role":29,"phone":49,"phoneExt":25,"email":31},"+31628129140",{"type":51,"investigatorFullName":52,"investigatorTitle":53,"investigatorAffiliation":5,"oldNameTitle":25,"oldOrganization":25},"PRINCIPAL_INVESTIGATOR","Majanka H. Heijenbrok-Kal, PhD","Assistant professor",[55,58],{"name":56,"class":57},"Rijndam Revalidatiecentrum","UNKNOWN",{"name":59,"class":6},"ZonMw: The Netherlands Organisation for Health Research and Development","100573662","implementation-of-a-home-based-computerized-cognitive-rehabilitation-program-for-patients-with-abi-100573662",false,"NCT06749197","Implementation of a Home-based Computerized Cognitive Rehabilitation Program for Patients With ABI","Implementation of a Home-based Computerized Cognitive Rehabilitation Program for Patients With Acquired Brain Injury","CoRe@Home","Inclusion Criteria:\n\n* diagnosed with acquired brain injury\n* receiving outpatient rehabilitation\n* sufficient command of Dutch or English language\n* internet access\n\nExclusion Criteria:\n\n* incapacitated patients like patients diagnosed with dementia","ALL","18 Years",{"count":71,"type":72},30,"ESTIMATED","INTERVENTIONAL",[75],"NA","Rationale: Patients with acquired brain injury (ABI) may suffer from persistent cognitive deficits and\u002For subjective cognitive complaints, especially in the domains of attention and working memory. Cognitive deficits are associated with anxiety and depression and may affect social participation and health-related quality of life (HR-QoL). Approximately 25% of the patients with ABI will be referred to an in- and\u002For outpatient rehabilitation center for multidisciplinary therapy to optimize recovery. Multiple studies suggest that supervised computerized cognitive training (CCT) may enhance cognitive functioning in patients with ABI. Recently, the CCT program RehaCom was introduced as an online version which is suitable for home training. In this study the feasibility and outcomes of implementing home-based CCT into a blended care pathway will be investigated in patients receiving outpatient rehabilitation therapy after ABI.\n\nObjective: The aim of this study is to assess the feasibility and to evaluate the effect of blending a home-based CCT program (RehaCom) in standard care on cognitive functioning in patients after ABI.\n\nThe secondary aim is to evaluate the effect of this CCT program on subjective cognitive complaints, self-efficacy, psychological outcome measures and HR-QoL.\n\nStudy design: Randomized cross-over trial comparing a 5-week blended care pathway to 5 weeks of standard care within 30 patients with ABI.\n\nStudy population: Adults with ABI receiving outpatient rehabilitation therapy.\n\nIntervention: A blended care pathway including 1 cognitive strategy training session of 1 hour per week in the outpatient rehabilitation center in combination with home-based CCT in 4 sessions of 30 minutes per week, during 5 weeks. The standard care pathway includes 2 cognitive training sessions of 1 hour per week in the outpatient rehabilitation center during 5 weeks.\n\nMain study parameters\u002Fendpoints: Cognitive functioning (attention and working memory), self-efficacy, psychological functioning (coping, anxiety, depression) and HR-QoL, using non-invasive neuropsychological tests and standardized online questionnaires. All outcomes will be assessed at baseline (T0), after 6 weeks (T1) and after 12 weeks (T2).\n\nNature and extent of the burden and risks associated with participation, benefit and group relatedness: In the blended care pathway patients will be instructed to follow a home-based CCT program. Training at home requires a time investment from patients but will also reduce the number of visits to the rehabilitation center. Participants can choose what time of the day is most convenient for them to engage in the program in their home environment instead of traveling to the rehabilitation center for scheduled cognitive training. Increasing patients' responsibility in their recovery process may improve their self-efficacy and HRQoL.\n\nCompletion of online questionnaires also requires a certain time investment from patients and might lead to temporary fatigue. Patients may take a break at any moment and continue completing the questionnaires at a later time. By a maximum duration of 45 to 60 minutes per measurement we aim to minimize the burden for patients. There are no risks associated with participation.",[78],"Acquired Brain Injury (Including Stroke)",[80,81,82,83,84,85],"cognition","cognitive impairment","attention deficit","memory disorder","computerized cognitive training","home-based training","2026-04-30",{"date":88,"type":89},"2026-05-01","ACTUAL",{"date":91,"type":89},"2025-03-20",{"date":93,"type":72},"2026-12-31",{"name":5,"class":6},1]