[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100612001":3},{"organization":4,"armGroups":7,"interventions":18,"overallOfficials":23,"centralContacts":27,"locations":12,"responsibleParty":32,"collaborators":12,"id":35,"slug":36,"hasResults":37,"nctId":38,"briefTitle":39,"officialTitle":40,"acronym":12,"eligibilityCriteria":41,"healthyVolunteers":37,"sex":42,"minAge":43,"maxAge":12,"enrollmentInfo":44,"targetDuration":12,"studyType":47,"phases":48,"briefSummary":50,"conditions":51,"keywords":53,"overallStatus":59,"whyStopped":12,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":12},{"fullName":5,"class":6},"Ankara Yildirim Beyazıt University","OTHER",[8,13],{"label":9,"type":10,"description":11,"interventionNames":12},"Control","NO_INTERVENTION","Patients who agree to participate in the study will be asked to complete a patient characteristics form. Patients in the control group will not receive any specific education from the researcher during the preoperative period. These patients will receive the clinic's routine patient education prior to surgery. After consulting with the nurses who provided the routine patient education at the clinic, the surgical fear scale will be administered. Upon arrival at the clinic after surgery, pain assessment will be performed using the VAS at 15 and 30 minutes, 1, 2, 4, 8, 12, and 24 hours. Since the data collection process for our study ends at 24 hours, the patient satisfaction scale will be completed at that time. Data collection is expected to take a total of 15-20 minutes.",null,{"label":14,"type":6,"description":15,"interventionNames":16},"Experimental","The researcher will provide patients with information about the virtual reality headset. The virtual reality headset will be disinfected before use for each patient. Patients in the experimental group will receive patient education using an animation-based video method with the virtual reality (VR) headset one day before the surgery. The training will be provided in a quiet, calm environment where the training will not be interrupted, in their own rooms for patients staying in single rooms, and in the nurse's room for patients staying in rooms with 2 or more beds. Patient education will be provided using the animation-based video method, and after answering the patient's questions, the surgical fear scale will be applied. Upon arrival at the clinic after surgery, pain assessment will be performed using the VAS at 15 and 30 minutes, 1, 2, 4, 8, 12, and 24 hours. Since the data collection process for our study ends at 24 hours, the patient satisfaction scale will be completed at that ti",[17],"Other: education",[19],{"type":6,"name":20,"description":21,"armGroupLabels":22,"otherNames":12},"education","The preparation of patient education using animation-based video methods will first involve the researcher developing a scenario based on the literature, covering the preoperative preparation process, deep breathing and coughing exercises, Respiratory Exercise Device use, pain management, potential postoperative complications, wound care, mobilization, and the rehabilitation process. After the educational content and its suitability are reviewed and approved by 5 experts and its content validity is established, it will be forwarded to a graphic design expert for the preparation of the animation. Regular feedback will be obtained throughout the video preparation process, and the work will be closely monitored. The voiceover for the animation video will be done by the researcher.",[14],[24],{"name":25,"affiliation":12,"role":26},"Kübra AYMELEK HACIOSMANOĞLU","PRINCIPAL_INVESTIGATOR",[28],{"name":25,"role":29,"phone":30,"phoneExt":12,"email":31},"CONTACT","+ 5546704908","kubraymlk@gmail.com",{"type":26,"investigatorFullName":33,"investigatorTitle":34,"investigatorAffiliation":5,"oldNameTitle":12,"oldOrganization":12},"KAHacıosmanoğlu","PhD student","100612001","the-impact-of-patient-education-delivered-through-virtual-reality-100612001",false,"NCT07247903","The Impact of Patient Education Delivered Through Virtual Reality","The Effect of Virtual Reality-Based Education on Preoperative Surgical Fear, Postoperative Pain and Patient Satisfaction in Patients Undergoing Knee Arthroplasty: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Be 18 years of age or older,\n* Agree to participate in volunteer work,\n* Have no communication problems in terms of vision, hearing, and perception,\n* Be able to read, speak, and understand Turkish,\n* Have no fear of enclosed spaces.\n\nExclusion Criteria:\n\n* Bilateral Total Knee Arthroplasty.\n* Admission to the clinic on the day of surgery.","ALL","18 Years",{"count":45,"type":46},70,"ESTIMATED","INTERVENTIONAL",[49],"NA","Objective: A randomized controlled trial was designed to determine the effect of virtual reality-based education provided to patients undergoing knee arthroplasty on preoperative surgical fear, postoperative pain, and patient satisfaction.\n\nMaterials and Methods: The study was designed as a randomized controlled experimental study, with the group receiving animation-based patient education via virtual reality goggles serving as the experimental group and the group receiving routine patient education at the clinic serving as the control group. Research data will be collected using a patient characteristics form prepared by the researcher based on a literature review, a surgical fear scale, a visual analog scale, and a patient education satisfaction scale. Virtual reality glasses will be used as the application tool in the study.",[52],"Knee Arthroplasty",[54,55,56,57,58],"virtual reality","pain","surgical fear","patient satisfaction","knee arthroplasty","NOT_YET_RECRUITING","2026-01-21",{"date":62,"type":63},"2026-01-22","ACTUAL",{"date":65,"type":46},"2026-01-12",{"date":67,"type":46},"2026-09-01",{"name":5,"class":6}]