[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100607876":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":24,"centralContacts":28,"locations":34,"responsibleParty":52,"collaborators":18,"id":56,"slug":57,"hasResults":58,"nctId":59,"briefTitle":60,"officialTitle":61,"acronym":18,"eligibilityCriteria":62,"healthyVolunteers":58,"sex":63,"minAge":64,"maxAge":18,"enrollmentInfo":65,"targetDuration":18,"studyType":68,"phases":69,"briefSummary":71,"conditions":72,"keywords":74,"overallStatus":79,"whyStopped":18,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":84,"completionDateStruct":86,"leadSponsor":88,"locationsCount":89},{"fullName":5,"class":6},"Ankara Yildirim Beyazıt University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"intervention Grubs","EXPERIMENTAL","The intervention group's surgical anxiety levels were assessed using the \"Surgical Anxiety Scale\" during the preoperative period. Subsequently, at the relevant clinic, the scale was administered twice on the day before the scheduled surgery date (at noon and in the evening) and once each at 48 and 72 hours post-surgery, for a total of four times. At the end of the application, the \"Surgical Anxiety Scale\" and the \"Surgical-Specific Anxiety Scale\" will be reapplied to the intervention group. In the postoperative period, participants' pain intensity will be measured using the \"NRS\" at 48 hours postoperatively before the intervention, immediately after the intervention, and at 72 hours before the intervention and immediately after the intervention.",[13],"Other: Guided imagery technique application",{"label":15,"type":16,"description":17,"interventionNames":18},"Control Grubs","NO_INTERVENTION","During the preoperative period, nursing care will be provided according to the routine care protocol of the clinic where the study is conducted. Subsequently, participants' levels of surgical anxiety will be assessed using the \"Anxiety Scale Specific to Surgery\" simultaneously with the intervention group patients. In the postoperative period, participants' pain intensity will be measured using the \"NRS\" at 48 and 72 hours postoperatively and will be measured again 60 minutes after the measurements (simultaneously with the intervention group patients). In the final stage, the analgesic consumption of the intervention and control groups will be evaluated on the 2nd and 3rd days of the postoperative period using the \"Analgesic Consumption Tracking Form\" to assess the administration status of the analgesic drugs included in the treatment protocol, and the application phase of the study will be completed.",null,[20],{"type":6,"name":21,"description":22,"armGroupLabels":23,"otherNames":18},"Guided imagery technique application","Intervention is a guided imagery technique designed for patients undergoing total joint arthroplasty. It will be administered in a total of 4 sessions: once daily on the day before surgery, twice daily on the day of surgery, and once daily on the 2nd and 3rd days after surgery, accompanied by imagery scenarios developed in accordance with the Compact Disc (CD) and literature developed by the Turkish Psychological Association. The study aims to examine its effects on surgical anxiety levels, postoperative pain intensity, and analgesic consumption. This approach is structured as a non-pharmacological method specific to surgical nursing practice and differs from previous similar studies in that it is applied in both the preoperative and postoperative periods using the same sample in the literature.",[9],[25],{"name":26,"affiliation":5,"role":27},"Gülay YAZICI, Assoc. Prof.","STUDY_DIRECTOR",[29],{"name":30,"role":31,"phone":32,"phoneExt":18,"email":33},"Büşra ERGEN TURAN, Lecturer","CONTACT","+90543810595","brergen62@gmail.com",[35],{"facility":36,"status":18,"city":37,"state":18,"zip":18,"country":38,"countryCode":18,"cosmosGeoPoint":39,"geoPoint":44,"contacts":45},"Zonguldak Atatürk State Hospital","Zonguldak","Turkey (Türkiye)",{"type":40,"coordinates":41},"Point",[42,43],31.79305,41.45139,{"lat":43,"lon":42},[46,49],{"name":36,"role":31,"phone":47,"phoneExt":18,"email":48},"0372 252 19 00","zonguldakdhs4@saglik.gov.tr",{"name":50,"role":51,"phone":18,"phoneExt":18,"email":18},"BÜŞRA ERGEN TURAN, Lecturer","PRINCIPAL_INVESTIGATOR",{"type":51,"investigatorFullName":53,"investigatorTitle":54,"investigatorAffiliation":55,"oldNameTitle":18,"oldOrganization":18},"BTuran","Lecturer","Zonguldak Bulent Ecevit University","100607876","the-effect-of-guided-imagery-technique-on-anxiety-pain-and-analgesic-use-in-total-joint-arthroplasty-patients-100607876",false,"NCT07194252","The Effect of Guided Imagery Technique on Anxiety, Pain, and Analgesic Use in Total Joint Arthroplasty Patients","The Effect of Guided Imagery Applied Before and After Surgery on Surgical Anxiety, Pain, and Analgesic Consumption in Patients Undergoing Total Joint Arthroplasty: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Patients who have undergone unilateral arthroplasty surgery,\n* Without cognitive impairment,\n* Who speak and write Turkish,\n* Without hearing or vision problems,\n* Without any other acute illness causing pain or anxiety,\n* Who received the same analgesic agent in the treatment protocol during the postoperative period,\n* And who volunteered to participate in the study will be included.\n\nExclusion Criteria:\n\n* Having a diagnosis of chronic pain syndrome or neuropathic pain,\n* Having a diagnosis of psychiatric illness\u002Fbeing under treatment\n* Continuous use of analgesic\u002Fsedative medication that may affect the pain threshold,\n* Hearing impairment or severe cognitive impairment that prevents participation in guided imagery applications.","ALL","18 Years",{"count":66,"type":67},128,"ESTIMATED","INTERVENTIONAL",[70],"NA","This randomized controlled study will investigate the effects of guided imagery on preoperative anxiety and postoperative pain and analgesic consumption in patients undergoing total joint arthroplasty. Conducted between September 2025 and June 2026 at a public hospital in Zonguldak, Turkey, the study will include patients scheduled for total joint arthroplasty following ethics committee approval. The intervention group will receive guided imagery twice preoperatively and once daily at 48 and 72 hours postoperatively. Outcomes will be assessed using the Surgical Anxiety Scale, surgery-specific anxiety scale, Numerical Rating Scale (NRS), and analgesic consumption tracking.",[73],"Total Joint Arthroplasty",[75,76,77,78],"pain","anxiety","analgesic","total joint arthroplasty","NOT_YET_RECRUITING","2025-09-18",{"date":82,"type":83},"2025-09-26","ACTUAL",{"date":85,"type":67},"2025-09-22",{"date":87,"type":67},"2026-06-22",{"name":5,"class":6},1]