[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100572893":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":18,"centralContacts":18,"locations":25,"responsibleParty":59,"collaborators":63,"id":70,"slug":71,"hasResults":72,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":76,"eligibilityCriteria":77,"healthyVolunteers":72,"sex":78,"minAge":79,"maxAge":80,"enrollmentInfo":81,"targetDuration":18,"studyType":84,"phases":85,"briefSummary":87,"conditions":88,"keywords":90,"overallStatus":95,"whyStopped":18,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":105},{"fullName":5,"class":6},"University of Campania Luigi Vanvitelli","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Virtual reality","ACTIVE_COMPARATOR","Participants will use the virtual reality during the standard dialysis session for 30 minutes, three times a week for 12 weeks.",[13],"Device: Virtual reality platform on head mounted display",{"label":15,"type":16,"description":17,"interventionNames":18},"Standard care","NO_INTERVENTION","Participants will perform the standard dialysis session three times a week for 12 weeks without virtual reality training sessions.",null,[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":18},"DEVICE","Virtual reality platform on head mounted display","Enhance Virtual Reality platform on a Meta Quest head mounted display",[9],[26,45],{"facility":27,"status":18,"city":28,"state":29,"zip":30,"country":31,"countryCode":32,"cosmosGeoPoint":33,"geoPoint":38,"contacts":39},"University of Bari","Bari","BA","70124","Italy","IT",{"type":34,"coordinates":35},"Point",[36,37],16.86982,41.12066,{"lat":37,"lon":36},[40],{"name":41,"role":42,"phone":43,"phoneExt":18,"email":44},"Giovanni Strippoli, Prof","CONTACT","0805591111","giovanni.strippoli@uniba.it",{"facility":46,"status":18,"city":47,"state":18,"zip":48,"country":31,"countryCode":32,"cosmosGeoPoint":49,"geoPoint":53,"contacts":54},"Univerity Vanvitelli","Naples","80133",{"type":34,"coordinates":50},[51,52],14.26811,40.85216,{"lat":52,"lon":51},[55],{"name":56,"role":42,"phone":57,"phoneExt":18,"email":58},"Davide Viggiano, Prof","0815664282","davide.viggiano@unicampania.it",{"type":60,"investigatorFullName":61,"investigatorTitle":62,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"PRINCIPAL_INVESTIGATOR","Davide Viggiano","Prof",[64,66,68],{"name":65,"class":6},"University of Sydney",{"name":67,"class":6},"University of Bari Aldo Moro",{"name":69,"class":6},"University of Otago","100572893","phase-2-virtual-reality-for-cognitive-impairment-in-hemodialysis-100572893",false,"NCT06739187","Virtual Reality for Cognitive Impairment in Hemodialysis","Virtual Reality Training for Cognitive Impairment in Adults Treated With Hemodialysis: A Feasibility Randomized Controlled Trial","VIRTUAL","Inclusion Criteria:\n\n* Adult participants aged 18 years or older and less than or equal to 75 years of age\n* Receiving haemodialysis treatment for kidney failure for at least 90 days (permanent reduction in kidney function below an estimated glomerular filtration rate of 15 mL\u002Fminute per 1.73 m2)\n* Able to provide written and informed consent\n* Able to use the immersive virtual reality headset and follow instructions with sufficient motor, visual and auditory function to interact with the intervention\n* Able to speak and understand Italian language\n\nExclusion Criteria:\n\n* Severe cognitive impairment or psychiatric diseases leading to inability to follow instructions and use the virtual reality headset\n* Significant nystagmus and\u002For vertigo leading to inability to tolerate the virtual reality headset\n* Insufficient motor function to use the virtual reality system\n* Hearing or visual disability\n* Advanced or uncompensated chronic diseases unrelated to kidney failure (e.g. advanced cancer, heart failure, lung diseases with poor oxygen saturation)\n* Other neurological diseases (ictus, Alzheimer's or other forms of dementia)\n* Persistent pain or itch or who using opioids that may interfere with the tests or any other condition that the clinician may judge as influencing the results","ALL","18 Years","75 Years",{"count":82,"type":83},60,"ESTIMATED","INTERVENTIONAL",[86],"PHASE2","The goal of this randomized feasibility clinical trial is to identify participant recruitment and retention, acceptability, and adherence to virtual reality training in people undergoing hemodialysis. The main question it aims to answer is if virtual reality could be a feasible and acceptable intervention in this setting.\n\nThe investigators will compare participants on virtual reality training during the standard dialysis session with those treated with standard dialysis session alone to see if a cognitive training using immersive virtual reality in people on hemodialysis is feasible and acceptable.\n\nParticipants randomised in the intervention group will use virtual reality during the standard dialysis session for 30 minutes, three times a week for 12 weeks. The virtual reality intervention will consist of computerized cognitive training of 4 games. Each exercise delivered to the participant will specifically provide training in a specific cognitive category (memory, cognitive flexibility, processing, attention, and memory). Participants randomised in the control group will perform the standard hemodialysis session three times a week for 12 weeks, without using virtual reality.",[89],"Hemodialysis",[91,92,93,94],"hemodialysis","virtual reality","RCT","kidney failure","NOT_YET_RECRUITING","2024-12-12",{"date":98,"type":99},"2024-12-18","ACTUAL",{"date":101,"type":83},"2025-04-01",{"date":103,"type":83},"2026-04-01",{"name":5,"class":6},2]