[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100542689":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":18,"centralContacts":24,"locations":30,"responsibleParty":46,"collaborators":18,"id":50,"slug":18,"hasResults":51,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":18,"eligibilityCriteria":55,"healthyVolunteers":51,"sex":56,"minAge":57,"maxAge":18,"enrollmentInfo":58,"targetDuration":18,"studyType":61,"phases":62,"briefSummary":64,"conditions":65,"keywords":18,"overallStatus":33,"whyStopped":18,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":79},{"fullName":5,"class":6},"Ente Ospedaliero Cantonale, Bellinzona","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Experimental Group","EXPERIMENTAL","In this group, virtual reality will be added to usual care",[13],"Device: Virtual reality application",{"label":15,"type":16,"description":17,"interventionNames":18},"Standard Group","NO_INTERVENTION","In this group, no extra intervention will be added to usual care",null,[20],{"type":21,"name":22,"description":11,"armGroupLabels":23,"otherNames":18},"DEVICE","Virtual reality application",[9],[25],{"name":26,"role":27,"phone":28,"phoneExt":18,"email":29},"Herve Schlotterbeck, MD","CONTACT","+41918115189","herve.schlotterbeck@eoc.ch",[31],{"facility":32,"status":33,"city":34,"state":35,"zip":36,"country":37,"cosmosGeoPoint":38,"geoPoint":43,"contacts":44},"Istituto CardioCentro","RECRUITING","Lugano","Canton Ticino","6900","Switzerland",{"type":39,"coordinates":40},"Point",[41,42],8.96004,46.01008,{"lat":42,"lon":41},[45],{"name":26,"role":27,"phone":28,"phoneExt":18,"email":29},{"type":47,"investigatorFullName":48,"investigatorTitle":49,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"SPONSOR_INVESTIGATOR","Schlotterbeck Hervé","Principal Investigator","100542689",false,"NCT06346132","Effect of Virtual Reality on Patient's Comfort During Cardiac Electronic Device Implantation.","Effect of Virtual Reality on Patient's Comfort During Cardiac Electronic Device Implantation: a Randomized, Controlled Trial.","Inclusion Criteria:\n\n* Patients over 18 year old,\n* Patients who signed the consent form and accepted to participate to the trial,\n* New cardiac electronic device implantation or cardiac electronic device battery change,\n* Surgical procedure planned in ambulatory care.\n\nExclusion Criteria:\n\n* Communication limitations,\n* Surgical procedure planned in sedation or narcosis,\n* Severe sensorial deficits (visual, auditory),\n* Claustrophobia,\n* Known motion sickness,\n* Patient isolated or with contact precautions,\n* Known or anticipated psychiatric diseases,\n* Patient known for epilepsia,\n* Opened scar and or ongoing infection at the level of the face and\u002For eyes,\n* Patient evaluated non suitable for the study by the surgeon, cardiologist or anesthetist.","ALL","18 Years",{"count":59,"type":60},150,"ESTIMATED","INTERVENTIONAL",[63],"NA","The purpose of this study is to assess the effect on patient's comfort of a virtual reality experience during a procedure of cardiac electronic device implantation under local anesthesia.",[66,67,68,69],"Virtual Reality","Medical Device","Local Anesthesia","Pain","2026-03-18",{"date":72,"type":73},"2026-03-20","ACTUAL",{"date":75,"type":73},"2024-03-29",{"date":77,"type":60},"2026-12-31",{"name":48,"class":6},1]