[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100627578":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":11,"centralContacts":20,"locations":26,"responsibleParty":45,"collaborators":11,"id":49,"slug":50,"hasResults":51,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":11,"eligibilityCriteria":55,"healthyVolunteers":51,"sex":56,"minAge":57,"maxAge":11,"enrollmentInfo":58,"targetDuration":11,"studyType":61,"phases":62,"briefSummary":64,"conditions":65,"keywords":11,"overallStatus":29,"whyStopped":11,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":78},{"fullName":5,"class":6},"Ente Ospedaliero Cantonale, Bellinzona","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Virtual reality arm","EXPERIMENTAL",null,[13],"Device: Virtual Reality",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":11},"DEVICE","Virtual Reality","The study intervention will take place on the day of surgery, in the ward, once patient's pre-operative preparation has been completed. The virtual reality device will be started according to the choices made by the patient (scenario and music) for a 20 min session. During that time, the patient will be left at rest and the interactions with the patient will be limited as much as possible.",[9],[21],{"name":22,"role":23,"phone":24,"phoneExt":11,"email":25},"Hervé Schlotterbeck, Medical Doctor","CONTACT","0041 91 811 51 89","herve.schlotterbeck@eoc.ch",[27],{"facility":28,"status":29,"city":30,"state":31,"zip":32,"country":33,"countryCode":34,"cosmosGeoPoint":35,"geoPoint":40,"contacts":41},"Istituto Cardiocentro","RECRUITING","Lugano","Canton Ticino","6900","Switzerland","CH",{"type":36,"coordinates":37},"Point",[38,39],8.96004,46.01008,{"lat":39,"lon":38},[42,43],{"name":22,"role":23,"phone":24,"phoneExt":11,"email":25},{"name":11,"role":23,"phone":44,"phoneExt":11,"email":11},"0041 91 811 50 00",{"type":46,"investigatorFullName":47,"investigatorTitle":48,"investigatorAffiliation":5,"oldNameTitle":11,"oldOrganization":11},"PRINCIPAL_INVESTIGATOR","Schlotterbeck Hervé","Medical Doctor","100627578","effect-of-virtual-reality-on-the-need-of-premedication-before-surgery-100627578",false,"NCT07450456","Effect of Virtual Reality on the Need of Premedication Before Surgery","Effect of Virtual Reality Immersion on the Need of Pharmacological Premedication Before Cardiac Surgery","Inclusion Criteria:\n\n* All patients undergoing elective surgery\n* Minimal age of 18-year-old\n* Able to give informed consent for the study\n* Requesting pharmacological premedication in the pre-operative period.\n\nExclusion Criteria:\n\n* Lacking capacity or ability to complete the consent form or to respond to the required obligations linked to the study protocol\n* Contraindications to pharmacological premedication\n* Known cognitive dysfunction, previous history of neurological\u002Fpsychiatric diseases like epilepsy\n* Non Italian speaking patients\n* Injuries to the head\u002Fface that would prohibit wearing headsets\n* Infectious skin conditions of the head\u002Fface\n* Contact isolation due to bacteria and viruses\n* Symptoms of vertigo or motion sickness\n* Reduced visual or auditory acuity\n* Pregnancy\n* Claustrophobia","ALL","18 Years",{"count":59,"type":60},40,"ESTIMATED","INTERVENTIONAL",[63],"NA","This study will assess, on patients requesting a pharmacological premedication in the preoperative period, if virtual reality reality could reduce the request of pharmacological premedication while maintaining a good level of comfort for the patient. The aim of this study is to understand if virtual reality could reduce the need for pharmacological premedication and their associated secondary effects.",[66,67,68,17],"Anxiety","Premedication","Surgery","2026-02-27",{"date":71,"type":72},"2026-03-04","ACTUAL",{"date":74,"type":72},"2025-11-11",{"date":76,"type":60},"2026-10",{"name":5,"class":6},1]