[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100643450":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":19,"centralContacts":23,"locations":33,"responsibleParty":49,"collaborators":52,"id":56,"slug":11,"hasResults":57,"nctId":58,"briefTitle":59,"officialTitle":60,"acronym":61,"eligibilityCriteria":62,"healthyVolunteers":57,"sex":63,"minAge":64,"maxAge":65,"enrollmentInfo":66,"targetDuration":11,"studyType":69,"phases":70,"briefSummary":72,"conditions":73,"keywords":76,"overallStatus":80,"whyStopped":11,"lastUpdateSubmitDate":81,"lastUpdatePostDateStruct":82,"startDateStruct":85,"completionDateStruct":87,"leadSponsor":89,"locationsCount":90},{"fullName":5,"class":6},"The University of Texas Health Science Center, Houston","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"VR sessions","EXPERIMENTAL",null,[13],"Device: VR sessions",[15],{"type":16,"name":9,"description":17,"armGroupLabels":18,"otherNames":11},"DEVICE","Participants will complete 3 supervised VR sessions using the Real System™ VR headset, per week for 6 weeks, for a total of 18 sessions. Each session will last approximately 60 minutes, with time allocated for setup and brief symptom checks",[9],[20],{"name":21,"affiliation":5,"role":22},"Seema Aggarwal, PhD, APRN, AGNP-C","PRINCIPAL_INVESTIGATOR",[24,29],{"name":25,"role":26,"phone":27,"phoneExt":11,"email":28},"Seema S Aggarwal, PhD, APRN, AGNP-C","CONTACT","(713) 500-9946","Seema.S.Aggarwal@uth.tmc.edu",{"name":30,"role":26,"phone":31,"phoneExt":11,"email":32},"Tela Todd","(713) 500-7039","Tela.Todd@uth.tmc.edu",[34],{"facility":35,"status":11,"city":36,"state":37,"zip":38,"country":39,"cosmosGeoPoint":40,"geoPoint":45,"contacts":46},"The University of Texas Health Science Center at Houston","Houston","Texas","77030","United States",{"type":41,"coordinates":42},"Point",[43,44],-95.36327,29.76328,{"lat":44,"lon":43},[47,48],{"name":21,"role":26,"phone":27,"phoneExt":11,"email":28},{"name":30,"role":26,"phone":31,"phoneExt":11,"email":32},{"type":22,"investigatorFullName":50,"investigatorTitle":51,"investigatorAffiliation":5,"oldNameTitle":11,"oldOrganization":11},"Seema S Aggarwal","Assistant Professor",[53],{"name":54,"class":55},"DPRIT Seed Grant","UNKNOWN","100643450",false,"NCT07638748","Feasibility, Usability, and Acceptability of Virtual Reality-Based Cognitive and Physical Rehabilitation in Individuals With Mild Cognitive Impairment","Feasibility, Usability, and Acceptability of Virtual Reality-Based Cognitive and Physical Rehabilitation in Individuals With Mild Cognitive Impairment (VR-MCI)","(VR-MCI)","Inclusion Criteria:\n\n* Clinical diagnosis of MCI (MoCA 18-26) or self-reported subjective cognitive decline (SCD)\n* Capacity to provide informed consent\n* Able to provide own transportation to sessions\n* Speaks and understands English\n* Ambulatory\n\nExclusion Criteria:\n\n* Uncontrolled seizures or epilepsy\n* Severe psychiatric illness or active suicidality\n* Inability to follow instructions or tolerate VR (severe motion sickness)\n* Cognitive impairment as a result of a known cause (e.g., dementia, stroke, Traumatic Brain Injury (TBI), medications, etc.)\n* Any condition that the research team determines would interfere with safe participation","ALL","55 Years","90 Years",{"count":67,"type":68},10,"ESTIMATED","INTERVENTIONAL",[71],"NA","The purpose of this study is to demonstrate feasibility, usability, and acceptability of VR-based cognitive and physical rehabilitation, evaluate adherence, tolerability, and fidelity to the VR intervention and explore preliminary effectiveness of VR-based rehabilitation on cognitive, physical, and functional outcomes",[74,75],"Mild Cognitive Impairment","Subjective Cognitive Decline (SCD)",[77,78,79],"Virtual Reality","Cognitive Rehabilitation","Physical Rehabilitation","NOT_YET_RECRUITING","2026-06-09",{"date":83,"type":84},"2026-06-10","ACTUAL",{"date":86,"type":68},"2026-06-12",{"date":88,"type":68},"2026-11-30",{"name":5,"class":6},1]