[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Niran Çoban\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":82},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,44,63],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100606089","the-effect-of-ney-music-on-patients-undergoing-lumbar-disc-surgery-100606089",false,"NCT07171008","The Effect of Ney Music on Patients Undergoing Lumbar Disc Surgery","The Effect of Ney Music on Pain, Anxiety, Sleep, and Quality of Life in Patients Undergoing Lumbar Disc Surgery","Inclusion Criteria:\n\n* Having undergone lumbar disc surgery under general anesthesia\n\n  * 18 years old and over,\n  * At least 3 hours have passed from the analgesic administration,\n  * Patients willing to participate in the study will be included in the study.\n\nExclusion Criteria:\n\n* Patient-controlled analgesia (PCA) is applied,\n\n  * Over 70 years old,\n  * Using anxiolytic and sedative drugs,\n  * Having a psychiatric illness,\n  * Patients with communication barriers will not be included in the study.",true,"ALL","18 Years","70 Years",{"count":21,"type":22},60,"ESTIMATED","INTERVENTIONAL",[25],"NA","This randomized controlled study aims to investigate the effects of ney music listening, a traditional Turkish wind instrument, on pain, anxiety, sleep quality, and vital signs in patients undergoing lumbar disc herniation surgery. Participants will be randomly assigned to intervention and control groups. The intervention group will receive a 15-minute ney music session at three different time points: preoperative (on the day of surgery), postoperative 3rd hour, and postoperative day 1. The control group will receive standard postoperative nursing care without music intervention. Data will be collected at the same time points in both groups using the Visual Analog Scale (VAS), State-Trait Anxiety Inventory (STAI-I), Richard-Campbell Sleep Questionnaire, and vital signs. The study seeks to evaluate the non-pharmacological benefits of therapeutic music in postoperative recovery.",[28,29,30],"Lumbar Disc Herniation","Surgery","Nurse's Role","RECRUITING","2025-11-23",{"date":34,"type":35},"2025-11-25","ACTUAL",{"date":37,"type":35},"2025-04-01",{"date":39,"type":22},"2025-12-01",{"name":41,"class":42},"Niran Çoban","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":51,"targetDuration":4,"studyType":23,"phases":52,"briefSummary":53,"conditions":54,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":56,"startDateStruct":58,"completionDateStruct":60,"leadSponsor":62,"locationsCount":43},"100601361","the-role-of-mandala-painting-before-surgery-100601361","NCT07109492","The Role of Mandala Painting Before Surgery","The Role of Mandala Painting Before Surgery on Anxiety and Stress","Inclusion Criteria:\n\n* Individuals who are undergoing elective surgery,\n* Cholecystectomy Surgery is planned\n\n  * Age 18 and over,\n  * Able to communicate,\n  * No wounds or injuries on their hands that would prevent them from painting,\n  * Volunteer to participate in the study.\n\nExclusion Criteria:\n\n* Individuals with a previous psychiatric diagnosis,\n\n  * Those with color blindness or visual perception disorders, Patients over 70 years of age\n  * Those taking tranquilizers (anxiolytics, antidepressants, etc.),\n  * Those with any health problems that may prevent them from painting (fractures, amputations, etc.),\n  * Those who are illiterate,\n  * Those with communication disabilities will be excluded from the study.",{"count":21,"type":22},[25],"Surgical interventions often cause significant anxiety and stress in patients during the preoperative period. In this study, it is aimed to determine the effect of mandala coloring, a non-pharmacological and art-based intervention, on reducing anxiety and stress levels in individuals scheduled for elective surgery. The universe of the study will consist of patients who will undergo elective surgery between June 2025 and June 2026 in the General Surgery Clinic of Istanbul Sultangazi Training and Research Hospital. Data will be collected using the Introductory Information Form, State Anxiety Inventory (STAI-S), Perceived Stress Scale (PSS), and Physiological Parameters Form (including blood pressure, pulse, respiration rate, and oxygen saturation). One day before surgery, patients who meet the inclusion criteria will be informed about the study and randomized into intervention and control groups using a random number table created with MS Excel software. Patients in the intervention group will perform a 20-minute mandala coloring activity in the preoperative waiting period. Before and after the application, participants' anxiety and stress levels will be evaluated with the STAI-S and PSS, and their physiological parameters will be recorded. Patients in the control group will receive standard preoperative care and will be evaluated at the same time points with the same tools, without any intervention. The study aims to provide evidence for the use of mandala coloring as a simple, low-cost, and effective nursing intervention to reduce preoperative anxiety and stress.",[55,29,30],"Mandala Painting",{"date":57,"type":35},"2025-11-28",{"date":59,"type":35},"2025-07-01",{"date":61,"type":22},"2026-12-01",{"name":41,"class":42},{"id":64,"slug":65,"hasResults":11,"nctId":66,"briefTitle":67,"officialTitle":68,"acronym":4,"eligibilityCriteria":69,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":70,"targetDuration":4,"studyType":23,"phases":71,"briefSummary":72,"conditions":73,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":79,"completionDateStruct":80,"leadSponsor":81,"locationsCount":43},"100601366","the-effect-of-baduanjin-on-patients-undergoing-knee-replacement-surgery-100601366","NCT07109557","The Effect of Baduanjin on Patients Undergoing Knee Replacement Surgery","The Effect of Baduanjin on Pain, Comfort, and Quality of Recovery in Patients Undergoing Knee Replacement Surgery","Inclusion Criteria:\n\n* Having undergone Knee Replacement Surgery under general anesthesia\n\n  • 18 years old and over,\n* Are in stable condition after surgery,\n* Are conscious, and\n* Volunteer to participate in the study.\n\nExclusion Criteria:\n\n* Patients with contraindications to Baduanjin exercises,\n\n  -• Over 70 years old,\n\n  • Using anxiolytic and sedative drugs,\n* Patients with any mental illness and those who do not meet the inclusion criteria will not be included in the study.",{"count":21,"type":22},[25],"This randomized controlled trial aims to evaluate the effects of Baduanjin, a traditional Chinese mind-body exercise, on pain, comfort, and quality of recovery in patients undergoing total knee arthroplasty (TKA). The study will be conducted between July 2025 and July 2026 at Yalova Training and Research Hospital's Orthopedics Clinic. Sixty patients will be randomly assigned into two groups: an intervention group practicing Baduanjin and a control group receiving standard postoperative care. The intervention will begin on the first postoperative day and continue for three weeks. Outcome measures include the Visual Analog Scale (VAS) for pain, the General Comfort Questionnaire, and the Quality of Recovery-40 (QoR-40) questionnaire. These assessments will be conducted weekly for three weeks. The control group will follow routine postoperative care without Baduanjin. The primary objective is to determine whether Baduanjin can improve postoperative outcomes in terms of pain reduction, increased comfort, and better recovery quality.",[74,29,75,30],"Pain, Postoperative","Knee Replacement","2025-08-07",{"date":78,"type":35},"2025-08-12",{"date":59,"type":35},{"date":61,"type":22},{"name":41,"class":42},""]