[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100501598":3},{"organization":4,"armGroups":7,"interventions":24,"overallOfficials":30,"centralContacts":34,"locations":43,"responsibleParty":87,"collaborators":89,"id":93,"slug":94,"hasResults":95,"nctId":96,"briefTitle":97,"officialTitle":98,"acronym":12,"eligibilityCriteria":99,"healthyVolunteers":100,"sex":101,"minAge":102,"maxAge":12,"enrollmentInfo":103,"targetDuration":12,"studyType":106,"phases":107,"briefSummary":109,"conditions":110,"keywords":112,"overallStatus":114,"whyStopped":12,"lastUpdateSubmitDate":115,"lastUpdatePostDateStruct":116,"startDateStruct":119,"completionDateStruct":121,"leadSponsor":123,"locationsCount":124},{"fullName":5,"class":6},"Weill Medical College of Cornell University","OTHER",[8,13,19],{"label":9,"type":10,"description":11,"interventionNames":12},"Project 1 - Phase 1: Development\u002FRefinement of VR program; Usability Testing\u002FDevelopment of Training","NO_INTERVENTION","The study includes one session that will last approximately 2 - 3 hours. The study involves completing some questionnaires that gather background demographic information and a structured needs assessment interview to gather information on user preferences, usability problems, implementation and training protocols.",null,{"label":14,"type":15,"description":16,"interventionNames":17},"Project 1 - Phase 2: VR Program","EXPERIMENTAL","Training will occur over 3 days and be conducted by research investigators in the participants' homes. Training will include training on the proper placement of the headset, the viewing lens, system headphones, and safety guidelines. The research investigator will aid in the set-up of the VR system in the home, which will be pre-loaded with applications, and will recommend an area to use the system to ensure a safe play area free of obstacles. Participants will be provided with practice tasks between training sessions. Participants will be provided with a \"hands-on\" performance assessment at the beginning of the second session and concepts\u002Fprocedures that are problematic will be reviewed. Participants will be contacted one-week post training to determine if they are having any problems by study investigators. Following training, participants will use the CAST VR program and tablet at will, though encouraged to use it at least three times per week for 20 minutes.",[18],"Behavioral: Project 1, Phase 2: VR Program for Social, Activity, and Cognitive Engagement",{"label":20,"type":21,"description":22,"interventionNames":23},"Project 1 - Phase 2: Tablet Control Condition","ACTIVE_COMPARATOR","Training will occur over 3 days and be conducted by research investigators in the participants' homes. Participants in the control condition will receive a tablet, internet support for 2 months and training (including training on cybersecurity). This will include instructions for accessing content similar to, but in 2-D, so less immersive than that included in the VR program (e.g., virtual museum tours, One click, etc.). Participants will complete all assessments and will be provided with an Android tablet that has a 10.1\" display, built in modem, and a front facing camera. Research investigators are providing people with tablets for standardization. Research Assessor (RA) Training, Certification and Treatment Fidelity. At follow-up assessments, assessors and data analysts will be blinded to treatment condition.",[18],[25],{"type":26,"name":27,"description":28,"armGroupLabels":29,"otherNames":12},"BEHAVIORAL","Project 1, Phase 2: VR Program for Social, Activity, and Cognitive Engagement","The investigators will apply a systematic approach to the design and evaluation of an immersive Cognitive Activity Social Technology (CAST) VR intervention (using the Oculus Quest 2), that provides aging adults a suite of virtual cognitive, social, and activity engagement applications. The program will allow for virtual interactions (one-on one or groups), cultural, creativity, and educational opportunities, and gaming.",[20,14],[31],{"name":32,"affiliation":5,"role":33},"Sara J Czaja, PhD","PRINCIPAL_INVESTIGATOR",[35,40],{"name":36,"role":37,"phone":38,"phoneExt":12,"email":39},"Chelsie Burchett, PhD","CONTACT","646-962-7141","cob2014@med.cornell.edu",{"name":41,"role":37,"phone":38,"phoneExt":12,"email":42},"Sophie Park","sep4008@med.cornell.edu",[44,57,73],{"facility":45,"status":12,"city":46,"state":47,"zip":48,"country":49,"countryCode":50,"cosmosGeoPoint":51,"geoPoint":56,"contacts":12},"Florida State University","Tallahassee","Florida","32306","United States","US",{"type":52,"coordinates":53},"Point",[54,55],-84.28073,30.43826,{"lat":55,"lon":54},{"facility":58,"status":12,"city":59,"state":60,"zip":61,"country":49,"countryCode":50,"cosmosGeoPoint":62,"geoPoint":66,"contacts":67},"University of Illinois Urbana-Champaign","Champaign","Illinois","61820",{"type":52,"coordinates":63},[64,65],-88.24338,40.11642,{"lat":65,"lon":64},[68,72],{"name":69,"role":37,"phone":70,"phoneExt":12,"email":71},"Wendy Rogers, PhD","217-300-1470","wendyr@illinois.edu",{"name":69,"role":33,"phone":12,"phoneExt":12,"email":12},{"facility":74,"status":12,"city":75,"state":75,"zip":76,"country":49,"countryCode":50,"cosmosGeoPoint":77,"geoPoint":81,"contacts":82},"Weill Cornell Medicine","New York","10065",{"type":52,"coordinates":78},[79,80],-74.00597,40.71427,{"lat":80,"lon":79},[83,85],{"name":84,"role":37,"phone":38,"phoneExt":12,"email":39},"Chelsie Burchett, MA",{"name":86,"role":33,"phone":12,"phoneExt":12,"email":12},"Sara Czaja, PhD",{"type":88,"investigatorFullName":12,"investigatorTitle":12,"investigatorAffiliation":12,"oldNameTitle":12,"oldOrganization":12},"SPONSOR",[90],{"name":91,"class":92},"National Institute on Aging (NIA)","NIH","100501598","center-for-research-and-education-on-aging-and-technology-enhancement---create-v---project-1-100501598",false,"NCT05811338","Center for Research and Education on Aging and Technology Enhancement - CREATE V - Project 1","Center for Research and Education on Aging and Technology Enhancement - CREATE V","Inclusion Criteria:\n\n* 65+ years of age\n* Able to read English at the 6th grade level\n* Have 20\u002F60 vision with or without correction.\n\nExclusion Criteria:\n\n* Blind or have visual impairments that limit their ability to view the technology.\n* Deaf or have hearing impairments that limit their ability to answer telephone queries.\n* Have a life-limiting\u002Fterminal illness\n* Severe motor impairment (e.g., severe tremors or debilitating arthritis in their hands) that impairs ability to speak or use dominant hand\n* Chronic neck pain\u002Finjury that might make the headset uncomfortable",true,"ALL","60 Years",{"count":104,"type":105},312,"ESTIMATED","INTERVENTIONAL",[108],"NA","Project 1: The goal of this research project is to examine usability and acceptance of virtual reality (VR) applications and their efficacy with older adults. This highly innovative cross-site Stage 1 Intervention Development Project (NIH (National Institutes of Health) Stage Model) will apply the CREATE systematic approach to the design and evaluation of an immersive VR program, Cognitive Activity Social Technology (CAST), for older adults. The program will provide a suite of virtual cognitive, social and activity engagement applications; and allow for virtual interactions.",[111],"Mild Cognitive Impairment",[113],"Technology","NOT_YET_RECRUITING","2026-05-12",{"date":117,"type":118},"2026-05-15","ACTUAL",{"date":120,"type":105},"2026-07-31",{"date":122,"type":105},"2027-05-31",{"name":5,"class":6},3]