[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100649236":3},{"organization":4,"armGroups":7,"interventions":24,"overallOfficials":23,"centralContacts":34,"locations":44,"responsibleParty":94,"collaborators":96,"id":100,"slug":101,"hasResults":102,"nctId":103,"briefTitle":104,"officialTitle":105,"acronym":106,"eligibilityCriteria":107,"healthyVolunteers":102,"sex":108,"minAge":109,"maxAge":23,"enrollmentInfo":110,"targetDuration":23,"studyType":113,"phases":114,"briefSummary":116,"conditions":117,"keywords":121,"overallStatus":47,"whyStopped":23,"lastUpdateSubmitDate":126,"lastUpdatePostDateStruct":127,"startDateStruct":130,"completionDateStruct":132,"leadSponsor":134,"locationsCount":135},{"fullName":5,"class":6},"Biogipuzkoa Health Research Institute","OTHER",[8,14,19],{"label":9,"type":10,"description":11,"interventionNames":12},"Computerized cognitive training - BrainHQ","EXPERIMENTAL","The arm will follow the cognitive training program BrainHQ.",[13],"Behavioral: Computerized cognitive treatment",{"label":15,"type":10,"description":16,"interventionNames":17},"Virtual Reality cognitive training - Enhance VR","The arm will follow the cognitive training program Enhance VR.",[18],"Behavioral: Virtual reality cognitive training",{"label":20,"type":21,"description":22,"interventionNames":23},"Control Group","NO_INTERVENTION","The arm will receive usual care with no cognitive intervention",null,[25,30],{"type":26,"name":27,"description":28,"armGroupLabels":29,"otherNames":23},"BEHAVIORAL","Computerized cognitive treatment","Online exercises that target the following functions: attention, processing speed, memory, spatial orientation, interpersonal skills and intelligence.\n\nParticipants will follow an online cognitive training with the BrainHQ program for 10 weeks. Patients will complete exercises that target attention, executive function, memory and processing speed. They will be asked to train approximately 30 minutes per BrainHQ session, 5 times per week for 10 weeks, a total of 25 hours. Training progresses in an adaptive way, based on the progression of the participant.",[9],{"type":26,"name":31,"description":32,"armGroupLabels":33,"otherNames":23},"Virtual reality cognitive training","A library of 15 cognitive exercises developed in virtual reality to train and monitor specific cognitive functions (memory, attention, task flexibility, information processing, orientation, and problem-solving) and motor control.\n\nParticipants will follow a virtual reality cognitive training with the Enhance VR program for 10 weeks. Patients will complete exercises that target attention, executive function, memory and processing speed. Participants will be asked to train approximately 30 minutes per Enhance VR session, 4 times per week for 10 weeks, a total of 20 hours. Training progresses in an adaptive way, based on the progression of the participant.",[15],[35,40],{"name":36,"role":37,"phone":38,"phoneExt":23,"email":39},"Dr. Ander Urruticoechea Ribate","CONTACT","+34943328000","ander.urruticoechearibate@osakidetza.eus",{"name":41,"role":37,"phone":42,"phoneExt":23,"email":43},"Dra. Mari Feli González","+34943328380","mariafeliciana.gonzalezperez@osakidetza.eus",[45,65,79],{"facility":46,"status":47,"city":48,"state":49,"zip":50,"country":51,"countryCode":52,"cosmosGeoPoint":53,"geoPoint":58,"contacts":59},"Hospital Universitario Basurto","RECRUITING","Bilbao","Bizkaia","48013","Spain","ES",{"type":54,"coordinates":55},"Point",[56,57],-2.92528,43.26271,{"lat":57,"lon":56},[60,61,62],{"name":36,"role":37,"phone":38,"phoneExt":23,"email":39},{"name":41,"role":37,"phone":42,"phoneExt":23,"email":43},{"name":63,"role":64,"phone":23,"phoneExt":23,"email":23},"Covadonga Figaredo Berjano, Dr.","PRINCIPAL_INVESTIGATOR",{"facility":66,"status":47,"city":67,"state":49,"zip":68,"country":51,"countryCode":52,"cosmosGeoPoint":69,"geoPoint":73,"contacts":74},"Hospital Universitario Galdakao-Usansolo","Galdakao","48960",{"type":54,"coordinates":70},[71,72],-2.8429,43.23073,{"lat":72,"lon":71},[75,76,77],{"name":36,"role":37,"phone":38,"phoneExt":23,"email":39},{"name":41,"role":37,"phone":42,"phoneExt":23,"email":43},{"name":78,"role":64,"phone":23,"phoneExt":23,"email":23},"Josefa Ferreiro Quintana, Dr.",{"facility":80,"status":47,"city":81,"state":82,"zip":83,"country":51,"countryCode":52,"cosmosGeoPoint":84,"geoPoint":88,"contacts":89},"Hospital Universitario Donostia","San Sebastián","Gipuzkoa","20014",{"type":54,"coordinates":85},[86,87],-5.9,43.56667,{"lat":87,"lon":86},[90,91,92],{"name":36,"role":37,"phone":38,"phoneExt":23,"email":39},{"name":41,"role":37,"phone":42,"phoneExt":23,"email":43},{"name":93,"role":64,"phone":23,"phoneExt":23,"email":23},"Ander Urruticoechea Ribate, Dr.",{"type":95,"investigatorFullName":23,"investigatorTitle":23,"investigatorAffiliation":23,"oldNameTitle":23,"oldOrganization":23},"SPONSOR",[97],{"name":98,"class":99},"Biobizkaia Health Research Institute","OTHER_GOV","100649236","early-cognitive-interventions-in-digital-format-for-cancer-survivors-100649236",false,"NCT07729969","Early Cognitive Interventions in Digital Format for Cancer Survivors","Early Cognitive Interventions in Digital Format for Cancer Survivors - INCOTEM","INCOTEM","Inclusion Criteria:\n\n* Patients over 18 years of age diagnosed with cancer (stage I-III)\n* Subjective complaints of cognitive functioning related to the diagnosis of cancer and\u002For cancer treatments\n* Between 1-6 months after completion of chemotherapy treatment\n* To have Wi-Fi and a computer\u002Ftablet\n* To sign the informed consent form\n\nExclusion Criteria:\n\n* Previous history of cancer diagnosis\n* Anticipated change in cancer treatment\u002Fgeneral medical treatment during the intervention period\n* Previous diagnosis of cognitive impairment\n* Diagnosis of other neurological or psychiatric diseases\n* Diagnosis of severe untreated depression\n* History of episodes of vertigo, epilepsy or seizures\n* Currently undergoing or having undergone any other type of intervention aimed at improving cognitive functioning (e.g., CRCI workshops)\n* Severe visual or hearing difficulties that may affect the performance of the intervention exercises\n* Inability to speak, understand, read, and write Spanish correctly\n* Failure to sign the informed consent form","ALL","18 Years",{"count":111,"type":112},110,"ESTIMATED","INTERVENTIONAL",[115],"NA","The aim of this study is to evaluate the usability and effectiveness of two professionally supervised home-based cognitive training interventions as part of an early rehabilitation protocol for cancer-related cognitive impairment.\n\nParticipants will be randomized to one of the two intervention arms (computerized cognitive intervention or virtual reality cognitive intervention) or to the control group. Participants of the intervention groups will be assessed before and after the 10 weeks intervention or at equivalent time points for the control group. Comparisons between experimental and control participants, and between the participants in the two intervention arms, will be carried out to see which intervention is most effective and accepted.",[118,119,120],"Cognitive Impairment","Cognitive Change","Cancer",[122,123,124,125],"Cancer Related Cognitive Impairment (CRCI)","Digital interventions","Computerized Cognitive Training","Virtual Reality Cognitive Training (VR)","2026-07-22",{"date":128,"type":129},"2026-07-28","ACTUAL",{"date":131,"type":129},"2026-06-08",{"date":133,"type":112},"2028-04-30",{"name":5,"class":6},3]