[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100584245":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":31,"centralContacts":36,"locations":42,"responsibleParty":62,"collaborators":26,"id":64,"slug":65,"hasResults":66,"nctId":67,"briefTitle":68,"officialTitle":69,"acronym":26,"eligibilityCriteria":70,"healthyVolunteers":66,"sex":71,"minAge":72,"maxAge":73,"enrollmentInfo":74,"targetDuration":26,"studyType":77,"phases":78,"briefSummary":80,"conditions":81,"keywords":83,"overallStatus":88,"whyStopped":26,"lastUpdateSubmitDate":89,"lastUpdatePostDateStruct":90,"startDateStruct":93,"completionDateStruct":95,"leadSponsor":97,"locationsCount":98},{"fullName":5,"class":6},"Uskudar University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"virtual reality","EXPERIMENTAL","Pre-Procedure: Information about the study will be given. Children with a pain score of '0' will be included in the groups. Verbal and written consent will be obtained from those who voluntarily agree to participate in the study. Video recording will be started with a mobile phone. Physiological parameters and anxiety level of the children will be measured and recorded 1 minute before the treatment. HFNC oxygen therapy will be started with video demonstration accompanied by virtual reality glasses. Physiological parameters and anxiety level will be recorded 10 minutes after HFNC oxygen treatment. Video recording will be terminated. Since the parameters in the scales should be evaluated by 2 nurses independent of the study during the study, only the behaviours of the child during the procedure should be video recorded by means of a mobile phone. For participants and parents who want to participate in the study but do not approve the video recording, the parameters will be evaluated ins",[13],"Device: Virtual reality goggles during HFNC",{"label":15,"type":16,"description":17,"interventionNames":18},"routine procedure","ACTIVE_COMPARATOR","Information about the study will be given. Children with a pain score of '0' will be included in the groups. Verbal and written consent will be obtained from those who voluntarily agree to participate in the study. Video recording will be started with a mobile phone. Physiological parameters and anxiety level of children will be measured and recorded 1 minute before the treatment. HFNC oxygen therapy will be started with routine ward practice. Physiological parameters and anxiety level will be recorded 10 minutes after HFNC oxygen treatment. Video recording will be terminated. Since the parameters in the scales should be evaluated by 2 nurses independent of the study during the research, only the behaviours of the child during the procedure should be video-recorded by means of a mobile phone. For participants and parents who want to participate in the study but do not approve the video recording, the parameters will be evaluated instantly by a researcher independent from the study.",[19],"Device: HFNC oxygen therapy with routine service application",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DEVICE","Virtual reality goggles during HFNC","HFNC oxygen therapy will be started with video demonstration accompanied by virtual reality glasses. Physiological parameters and anxiety level will be recorded 10 minutes after HFNC oxygen treatment. Video recording will be terminated. Since the parameters in the scales should be evaluated by 2 nurses independent of the study during the study, only the behaviours of the child during the procedure should be video recorded by a mobile phone. For the participants and parents who want to participate in the study but do not approve the video recording, the parameters will be evaluated instantly by a researcher independent from the study. The study will continue until the 30-person intervention group is completed.",[9],null,{"type":22,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"HFNC oxygen therapy with routine service application","HFNC oxygen therapy will be started with routine ward practice. Physiological parameters and anxiety level will be recorded 10 minutes after HFNC oxygen treatment. Video recording will be terminated. Since the parameters in the scales should be evaluated by 2 nurses independent of the study during the research, only the behaviours of the child during the procedure should be video-recorded by means of a mobile phone. For participants and parents who want to participate in the study but do not approve the video recording, the parameters will be evaluated instantly by a researcher independent from the study",[15],[32],{"name":33,"affiliation":34,"role":35},"Tuğba KARAKUŞ TÜRKER","Üsküdar University Faculty of Health Sciences","STUDY_DIRECTOR",[37],{"name":38,"role":39,"phone":40,"phoneExt":26,"email":41},"Tuğba KARAKAYA","CONTACT","+905435701207","tuggbbakarakaya@gmail.com",[43],{"facility":44,"status":26,"city":45,"state":46,"zip":26,"country":47,"countryCode":26,"cosmosGeoPoint":48,"geoPoint":53,"contacts":54},"Şehit Prof. Dr. İlhan Varank Sancaktepe Training and Research Hospital","Istanbul","Sancaktepe","Turkey (Türkiye)",{"type":49,"coordinates":50},"Point",[51,52],28.94966,41.01384,{"lat":52,"lon":51},[55,59],{"name":56,"role":39,"phone":57,"phoneExt":26,"email":58},"İlhan Varank Sancaktepe Training and Research Hospital Training and Research Hospital","+902166063300","istanbuleah35.bsh@saglik.gov.tr",{"name":60,"role":61,"phone":26,"phoneExt":26,"email":26},"Tuğba Karakaya","PRINCIPAL_INVESTIGATOR",{"type":61,"investigatorFullName":60,"investigatorTitle":63,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"Principal Investigator","100584245","virtual-reality-application-during-high-flow-nasal-oxygen-therapy-in-children-effect-on-anxiety-levels-100584245",false,"NCT06886828","Virtual Reality Application During High Flow Nasal Oxygen Therapy in Children Effect on Anxiety Levels","Virtual Reality Application During High Flow Nasal Oxygen Therapy in Children Effect on Anxiety Levels: A Randomised Controlled Study","Inclusion Criteria:\n\n* The child is between 6-12 years old\n* The child is receiving high flow nasal cannula oxygen therapy in the paediatric intensive care unit\n* The child has no visual and hearing problems\n* No pain according to the Wong-Baker pain scale\n* No genetic, congenital, chronic or metabolic disease\n* Being conscious and able to communicate verbally\n* Written and verbal acceptance of the child and his\u002Fher parents to participate in the study after the information.\n\nExclusion Criteria:\n\n* The child is in pain.\n* The child is taking a sedative medication\n* The child has a fever above 37°C\n* The child presented with a severe asthma attack\n* The child's saturation value was below 92% at the time of admission","ALL","6 Years","12 Years",{"count":75,"type":76},60,"ESTIMATED","INTERVENTIONAL",[79],"NA","Determination of the effect of virtual reality goggles used during high-flow oxygen therapy on child anxiety in children",[82],"Respiratory Distress",[84,9,85,86,87],"high flow nasal oxygen therapy","Anxiety","distraction of attention","child","NOT_YET_RECRUITING","2025-03-22",{"date":91,"type":92},"2025-03-26","ACTUAL",{"date":94,"type":76},"2025-04",{"date":96,"type":76},"2026-04",{"name":5,"class":6},1]