[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100646601":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":25,"centralContacts":29,"locations":39,"responsibleParty":57,"collaborators":18,"id":60,"slug":61,"hasResults":62,"nctId":63,"briefTitle":64,"officialTitle":65,"acronym":66,"eligibilityCriteria":67,"healthyVolunteers":62,"sex":68,"minAge":69,"maxAge":70,"enrollmentInfo":71,"targetDuration":18,"studyType":74,"phases":75,"briefSummary":77,"conditions":78,"keywords":84,"overallStatus":42,"whyStopped":18,"lastUpdateSubmitDate":88,"lastUpdatePostDateStruct":89,"startDateStruct":92,"completionDateStruct":94,"leadSponsor":96,"locationsCount":97},{"fullName":5,"class":6},"Adiyaman University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Experimental Group","EXPERIMENTAL","Participants in the experimental group will undergo a virtual reality headset intervention. This intervention will be administered to patients in the clinic during the acute phase-the first 48 hours following total hip replacement surgery. The scales used in the study will be administered twice: once before and once after the intervention.",[13],"Behavioral: cognitive intervention",{"label":15,"type":16,"description":17,"interventionNames":18},"Control Group","NO_INTERVENTION","Participants in the control group will receive standard care. The intervention will be administered to patients who are in the clinic during the acute phase-the first 48 hours-following total hip replacement surgery. The scales used in the study will be administered twice: once before and once after the intervention.",null,[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":18},"BEHAVIORAL","cognitive intervention","The patient undergoing the virtual reality session will lie in a supine position, supported and comfortable, with the head elevated at an angle of 30˚-45˚. The content will feature nature sounds and soothing background music; three different segments will be programmed: a forest or beach landscape, an underwater scene, and an outdoor excursion. Each option consists of 30 minutes of footage. The patient will select their preferred footage from these options, and after the sound settings are adjusted to a level the patient finds comfortable and non-disturbing, the session will begin and last for 30 minutes. Following the session, data will be collected in a face-to-face setting.",[9],[26],{"name":27,"affiliation":5,"role":28},"OĞUZHAN ÇAĞLAR, MSc Std","PRINCIPAL_INVESTIGATOR",[30,35],{"name":27,"role":31,"phone":32,"phoneExt":33,"email":34},"CONTACT","5423455495","+90","ocaglar@adiyaman.edu.tr",{"name":36,"role":31,"phone":37,"phoneExt":33,"email":38},"BİLSEV DEMİR, Assoc. Prof.","5364083761","bilsev.demir@ozal.edu.tr",[40],{"facility":41,"status":42,"city":43,"state":18,"zip":44,"country":45,"countryCode":18,"cosmosGeoPoint":46,"geoPoint":51,"contacts":52},"Malatya Turgut Özal University","RECRUITING","Malatya","44900","Turkey (Türkiye)",{"type":47,"coordinates":48},"Point",[49,50],38.31667,38.35018,{"lat":50,"lon":49},[53],{"name":54,"role":31,"phone":55,"phoneExt":33,"email":56},"Malatya Turgut Özal Medical Center","4228461255","ilker.ayten@ozal.edu.tr",{"type":28,"investigatorFullName":58,"investigatorTitle":59,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"Oğuzhan Çağlar","Research Assistant","100646601","vr-effects-after-hip-replacement-surgery-pain-100646601",false,"NCT07689461","VR Effects After Hip Replacement Surgery Pain","The Effect of Virtual Reality on Pain, Anxiety, and Comfort Levels After Total Hip Replacement Surgery","THA","Inclusion Criteria:\n\n* Patients scheduled for elective surgery who agree to participate in the study,\n* Individuals 18 years of age or older,\n* Those with adequate cognitive function,\n* Those who have not previously undergone total hip replacement surgery,\n* Those who volunteer to participate in the study and sign the informed consent form,\n* Patients with a pain score (on a scale of 1 to 10) of 4 or higher were included in the study.\n\nExclusion Criteria:\n\n* Individuals under the age of 18,\n* Those previously diagnosed with a chronic pain syndrome (other than hip osteoarthritis),\n* Individuals with impaired cognitive function (severe psychiatric disorders),\n* Individuals who have previously undergone total hip replacement surgery,\n* Individuals with severe hearing or visual impairments,\n* Individuals with a history of opioid dependence,\n* Patients with a pain score (on a scale of 1 to 10) of 4 or lower were excluded from the study.","ALL","18 Years","99 Years",{"count":72,"type":73},80,"ESTIMATED","INTERVENTIONAL",[76],"NA","Total Hip Arthroplasty (THA), a procedure performed to enhance the quality of life, is accompanied by postoperative challenges such as pain and anxiety that adversely affect patient comfort. Inadequate management of these complications can prolong the length of hospital stay, delay recovery, lead to functional impairments, and elevate the risk of chronic pain development. Conventional pharmacological interventions employed for management are limited due to their potential for adverse effects and dependency. Virtual reality (VR) is a non-pharmacological distraction technique utilized in the healthcare sector, leveraging advanced technology to maximize patient comfort by alleviating pain and minimizing anxiety.\n\nA review of the literature reveals that while the use of VR has positive effects on pain and anxiety, there is a notable scarcity of high-quality randomized controlled trials concurrently evaluating its impact on pain, anxiety, and comfort levels in postoperative orthopedic procedures such as THA. In this randomized controlled trial, participants in the control group will receive standard care, whereas those in the experimental group will receive a 30-minute VR intervention-offering three distinct options-in addition to standard care during the acute phase of the first 48 hours. Postoperative assessments will be conducted using the Visual Analogue Scale (VAS) for pain intensity, the State Anxiety Inventory for anxiety levels, and the Perianesthesia Comfort Scale for comfort levels.\n\nBy evaluating the potential of VR as a non-pharmacological adjuvant in post-THA care, the findings of this study will provide significant contributions to evidence-based nursing practices aimed at developing multimodal pain management strategies, reducing opioid consumption, and enhancing patient satisfaction.",[79,80,81,82,83],"Virtual Reality","Hip Arthropathy","Comfort","Anxiety","Pain, Postoperative",[79,85,86,82,87],"Total Hip Arthroplasty","Postoperative Pain","Comfort Level","2026-07-01",{"date":90,"type":91},"2026-07-08","ACTUAL",{"date":93,"type":91},"2025-10-21",{"date":95,"type":73},"2026-12-31",{"name":5,"class":6},1]