[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100587011":3},{"organization":4,"outcomesModule":7,"designInfo":22,"detailedDescription":31,"studyPopulation":21,"armGroups":32,"interventions":47,"overallOfficials":58,"centralContacts":62,"locations":21,"responsibleParty":68,"collaborators":21,"id":71,"slug":21,"hasResults":72,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":21,"eligibilityCriteria":76,"healthyVolunteers":72,"sex":77,"minAge":78,"maxAge":79,"enrollmentInfo":80,"targetDuration":21,"studyType":83,"phases":84,"briefSummary":86,"conditions":87,"keywords":89,"overallStatus":94,"whyStopped":21,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":21},{"fullName":5,"class":6},"Weifang Medical University","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":21,"otherOutcomes":21},[9,13,17],{"measure":10,"description":11,"timeFrame":12},"Pain response","The Visual Analog Scale (VAS) scale was used to assess the pain response of patients.","The pain response of patients was assessed at 0.5 hour, 3 hour, 6 hour, 12 hour, 24 hour postoperatively, and immediately after intervention.",{"measure":14,"description":15,"timeFrame":16},"Anxiety","The Beck Anxiety Inventory (BAI) scale was used to assess the anxiety of patients.","The anxiety level of patients was assessed immediately after the intervention.",{"measure":18,"description":19,"timeFrame":20},"Sleep quality","The Pittsburgh Sleep Quality Index (PSQI) scale was used to assess the postoperative sleep quality of patients.","The sleep quality of patients was assessed at 24 hour postoperatively.",null,{"allocation":23,"interventionModel":24,"interventionModelDescription":21,"primaryPurpose":25,"observationalModel":21,"timePerspective":21,"maskingInfo":26},"RANDOMIZED","PARALLEL","SUPPORTIVE_CARE",{"masking":27,"maskingDescription":21,"whoMasked":28},"DOUBLE",[29,30],"INVESTIGATOR","OUTCOMES_ASSESSOR","This study explores the effectiveness of a virtual reality-based multisensory intervention for postoperative recovery in patients receiving gynecological surgery. The results of the study included postoperative pain response, comfort, and anxiety of the patients.",[33,39,43],{"label":34,"type":6,"description":35,"interventionNames":36},"VR-Aromatherapy group","The VR-Aromatherapy group received virtual reality intervention combined with aromatherapy for 20 minutes postoperatively. The intervention was started by an investigator from the return of the patient to the ward.",[37,38],"Other: Virtual Reality intervention","Other: Aromatherapy",{"label":40,"type":6,"description":41,"interventionNames":42},"Aromatherapy group","The Aromatherapy group received lavender aromatherapy for 20 minutes postoperatively. The intervention was started by an investigator from the return of the patient to the ward.",[38],{"label":44,"type":6,"description":45,"interventionNames":46},"VR group","The VR group received virtual reality intervention for 20 minutes postoperatively. The intervention was started by an investigator from the return of the patient to the ward.",[37],[48,54],{"type":6,"name":49,"description":50,"armGroupLabels":51,"otherNames":52},"Virtual Reality intervention","The head-mounted virtual reality device is used to provide patients with relaxing videos of nature scenes accompanied by calming music and guided meditations.",[44,34],[53],"VR intervention",{"type":6,"name":55,"description":56,"armGroupLabels":57,"otherNames":21},"Aromatherapy","The cotton ball soaked in lavender essential oil is placed near the patient's pillow.",[40,34],[59],{"name":60,"affiliation":5,"role":61},"Jiang Liu, M.D","PRINCIPAL_INVESTIGATOR",[63],{"name":64,"role":65,"phone":66,"phoneExt":21,"email":67},"Shirong Fang, M.D","CONTACT","15094947165","fsr0536@163.com",{"type":61,"investigatorFullName":69,"investigatorTitle":70,"investigatorAffiliation":5,"oldNameTitle":21,"oldOrganization":21},"Jiang Liu","Research investigator","100587011",false,"NCT06922838","The Effectiveness of a Virtual Reality-based Multisensory Intervention","Effectiveness of a Virtual Reality-based Multisensory Intervention for Postoperative Recovery in Patients Receiving Gynecological Surgery","Inclusion Criteria: 1) significant postoperative pain response (VAS score over 4); 2) age greater than 18 years and volunteered to participate in this study.\n\nExclusion Criteria: 1) patients with psychosomatic disorders such as delirium, schizophrenia, and bipolar disorder; 2) patients with epilepsy, motion sickness, lightsensitivity, or other neurological diseases may have difficulty wearing the VR headset; 3) patients have severe heart, liver, kidney, blood, digestive, and nervous diseases.","FEMALE","18 Years","75 Years",{"count":81,"type":82},100,"ESTIMATED","INTERVENTIONAL",[85],"NA","This study explores the effectiveness of a virtual reality-based multisensory intervention for postoperative recovery in patients receiving gynecological surgery.",[88],"Gynecological Disease",[90,91,92,93],"Pain management","Virtual reality","Gynecology","Postoperative recovery","NOT_YET_RECRUITING","2025-04-09",{"date":97,"type":98},"2025-04-11","ACTUAL",{"date":100,"type":82},"2025-04-06",{"date":102,"type":82},"2025-08-01",{"name":5,"class":6}]