[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"surgical-nursing\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:surgical-nursing":34},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,51,94],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":37,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":46,"leadSponsor":48,"locationsCount":4},"100631668","cabg-ai-supported-discharge-education-100631668",false,"NCT07503678","CABG-AI-Supported Discharge Education","The Effect of Artificial Intelligence-Supported Individualized Discharge Education on Postoperative Pain, Anxiety, Stress Response, Recovery, and Discharge Education Satisfaction in Patients Undergoing Coronary Artery Bypass Graft Surgery: A Randomized Controlled Trial","AI-D-E-CABG","Inclusion Criteria:\n\n* Patients who have undergone coronary artery bypass graft (CABG) surgery.\n* Age 18 years or older.\n* Hemodynamically stable at the time of enrollment.\n* Able to understand and communicate in Turkish.\n* Able to use or have access to a mobile phone capable of viewing the educational video.\n* Able to provide informed consent.\n* Scheduled for routine postoperative follow-up at the study hospital.\n\nExclusion Criteria:\n\n* Patients undergoing emergency CABG surgery.\n* Presence of severe cognitive impairment that prevents understanding or following instructions.\n* Diagnosed psychiatric disorders (e.g., schizophrenia, severe depression) that interfere with study participation.\n* Severe vision or hearing impairment that prevents receiving the education.\n* Presence of postoperative complications requiring intensive care readmission.\n* Patients with endocrine disorders affecting stress biomarkers (e.g., Cushing's syndrome, Addison's disease).\n* Chronic use of corticosteroids or medications that significantly alter cortisol levels.\n* Patients who decline to participate or withdraw consent.\n* Patients who are unable to complete follow-up assessments.","ALL","18 Years",{"count":20,"type":21},128,"ESTIMATED","INTERVENTIONAL",[24],"NA","This randomized controlled trial will evaluate the effectiveness of artificial intelligence-supported individualized discharge education for patients undergoing coronary artery bypass graft (CABG) surgery. Participants will be assigned to either the intervention group, which will receive personalized AI-generated discharge education delivered through a nurse-avatar video in addition to standard verbal education, or the control group, which will receive standard discharge education only. The study will compare postoperative pain, anxiety, physiological stress response, recovery, and satisfaction with discharge education between the two groups. Outcomes will be measured during hospitalization and at the routine postoperative follow-up visit. The findings may help improve patient education methods and postoperative recovery in cardiac surgery patients.",[27,28,29,30,31,32,33,34,35,36],"Coronary Artery Disease","Postoperative Care","Patient Discharge","Recovery of Function","Anxiety","Pain","Stress, Physiological","Surgical Nursing","Nursing","Discharge Education",[27,28,29,38,34],"discharge education","NOT_YET_RECRUITING","2026-03-25",{"date":42,"type":43},"2026-03-31","ACTUAL",{"date":45,"type":21},"2026-06-01",{"date":47,"type":21},"2027-02-01",{"name":49,"class":50},"Hasan Kalyoncu University","OTHER",{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":4,"eligibilityCriteria":57,"healthyVolunteers":11,"sex":17,"minAge":58,"maxAge":4,"enrollmentInfo":59,"targetDuration":61,"studyType":62,"phases":4,"briefSummary":63,"conditions":64,"keywords":74,"overallStatus":83,"whyStopped":4,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":93},"100617738","smartwatch-accuracy-for-measuring-vitals-and-anxiety-before-disc-surgery-100617738","NCT07322523","Smartwatch Accuracy for Measuring Vitals and Anxiety Before Disc Surgery","Validation of Smartwatch Technology for Preoperative Monitoring of Sleep Quality, Anxiety, and Vital Signs in Patients Undergoing Disc Herniation Surgery","Inclusion Criteria:\n\n* 22 years and older\n* Currently receiving preoperative care\u002Fassessment for disc herniation surgery.\n* No history of any cardiovascular disease other than controlled hypertension.\n* Willingness to wear the smartwatch for a minimum of 8 consecutive hours during the night before surgery.\n* Ability to follow all instructions related to the smartwatch operation and data collection independently.\n* No known allergy to nickel.\n\nExclusion Criteria:\n\n* Patients who are currently receiving prescribed medication specifically for sleep in the clinical setting.\n* Refusal or unwillingness to participate in the study.\n* The participant fails to wear the smartwatch correctly or appropriately as per study instructions, leading to incomplete or unreliable data collection.","22 Years",{"count":60,"type":21},60,"3 Months","OBSERVATIONAL","This study aims to verify the accuracy of blood pressure, heart rate, blood oxygen saturation, anxiety level, and sleep cycle data measurements obtained from Samsung smartwatches compared to the currently accepted method used in patients with disc herniation undergoing the preoperative period.",[65,66,67,68,69,70,71,72,73,34],"Disc Herniations","Disc Herniation, Lumbar","Cervical Disc Herniation","Preoperative Anxiety Score","Sleep Quality","Preoperative Care","Vital Signs Monitoring","Smart Watch","Wearable Devices",[75,76,77,78,79,80,81,82],"Disc herniations","wearable devices","smart watch","vital signs monitoring","sleep quality","anxiety","surgical nursing,","preoperative","RECRUITING","2025-12-22",{"date":86,"type":43},"2026-01-07",{"date":88,"type":43},"2025-11-01",{"date":90,"type":21},"2026-03-30",{"name":92,"class":50},"Halil Kalaycı",1,{"id":95,"slug":96,"hasResults":11,"nctId":97,"briefTitle":98,"officialTitle":99,"acronym":4,"eligibilityCriteria":100,"healthyVolunteers":101,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":102,"targetDuration":4,"studyType":22,"phases":104,"briefSummary":105,"conditions":106,"keywords":4,"overallStatus":83,"whyStopped":4,"lastUpdateSubmitDate":112,"lastUpdatePostDateStruct":113,"startDateStruct":115,"completionDateStruct":117,"leadSponsor":119,"locationsCount":93},"100548046","effect-of-4-7-8-breathng-technque-on-shoulder-pan-and-respratory-functon-tests-after-laparoscopc-cholesectectomy-100548046","NCT06415890","Effect of 4-7-8 Breathıng Technıque on Shoulder Paın and Respıratory Functıon Tests After Laparoscopıc Cholesectectomy","The Effect of Usıng The 4-7-8 Breathıng Technıque on Postoperatıve Shoulder Paın and Respıratory Functıon Tests After Laparoscopıc Cholecystectomy","Inclusion Criteria:\n\n* Undergoing elective laparoscopic cholecystectomy,\n* Admitted to the clinic at least 2 hours before the surgical procedure,\n* Open to communication and cooperation,\n* Written and verbal permission to participate in the study was obtained,\n* Conscious, oriented and cooperative,\n* No cognitive and mental problems,\n* Speaks and understands Turkish,\n* American Society of Anesthesiologists (ASA) classification scores of I and II,\n* Hospitalized at least one night after surgical intervention,\n* Patients aged 18 years and older will be included in the study.\n\nExclusion Criteria:\n\n* Undergoing emergency laparoscopic cholecystectomy,\n* Open cholecystectomy,\n* Not admitted to the clinic at least 2 hours before the surgical procedure,\n* Not open to communication and cooperation,\n* Written and verbal permission to participate in the research could not be obtained,\n* Unconscious, disoriented and uncooperative,\n* Cognitively and mentally impaired,\n* Speaking Turkish but not understanding it,\n* Discharged on the same day after surgical intervention,\n* ASA score III and above,\n* Patients aged 18 years and younger will not be included in the study.",true,{"count":103,"type":21},98,[24],"This study was planned as a randomized controlled clinical trial to determine the effect of 4-7-8 breathing technique on shoulder pain and pulmonary function tests after laporoscopic cholecystectomy. A sample of 96 patients will be randomly assigned to the study and control groups. The study group will be administered the 4-7-8 breathing technique after LK, while the control group will be given routine care of the ward. Shoulder pain and pulmonary function tests will be measured in the first 24 hours and at discharge. The data obtained will be analyzed by appropriate statistical methods.",[107,108,109,110,34,111],"Laparoscopic Cholecystectomy","Breathing Exercise","Pulmonary Function Test","Shoulder Pain","4-7-8 Breathing Technique","2024-09-07",{"date":114,"type":43},"2024-09-19",{"date":116,"type":43},"2024-08-25",{"date":118,"type":21},"2025-07-15",{"name":120,"class":50},"Mustafa Kemal University"]