[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Gamze BULUT\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":91},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,46,70],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":4},"100625803","effect-of-podcast-based-education-on-preoperative-nursing-competency-and-evidence-based-knowledge-in-nursing-students-100625803",false,"NCT07427381","Effect of Podcast-Based Education on Preoperative Nursing Competency and Evidence-Based Knowledge in Nursing Students","The Use of Podcasts in Nursing Education: Evaluating the Acquisition of Competency and Evidence-Based Knowledge in Preoperative Preparation","Inclusion Criteria:\n\n* Age 18 years or older\n* Undergraduate nursing student enrolled in the course (second-year nursing students in the Faculty of Nursing)\n* Willing to participate and provides written and verbal informed consent\n\nExclusion Criteria:\n\n* Does not agree to participate or declines consent\n* Withdraws from the study at any time after enrollment",true,"ALL","18 Years",{"count":20,"type":21},80,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study aims to evaluate the effectiveness of podcast-based education on nursing students' competency in preoperative patient care and their knowledge of evidence-based nursing practices. Preoperative care is a critical component of perioperative nursing and plays a key role in patient safety and surgical outcomes. Improving students' competency in this area is essential for maintaining quality care.\n\nIn this quasi-experimental controlled study, undergraduate nursing students will be randomly assigned to either a control group receiving standard classroom education or an intervention group receiving standard education supplemented with structured podcast materials focusing on preoperative patient preparation and assessment. Outcomes will be measured using validated competency and knowledge assessment tools administered before and four weeks after the educational intervention.\n\nThe study is designed as a minimal-risk educational intervention and seeks to determine whether podcast-based learning can enhance competency and evidence-based knowledge in nursing education.",[27,28,29,30],"Preoperative Care","Nursing Education","Podcast","Evidence Based Nursing",[32,29,33],"Preoperative education","Nursing student","NOT_YET_RECRUITING","2026-02-20",{"date":37,"type":38},"2026-02-23","ACTUAL",{"date":40,"type":21},"2026-02-28",{"date":42,"type":21},"2026-04-28",{"name":44,"class":45},"Gamze BULUT","OTHER",{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":22,"phases":56,"briefSummary":57,"conditions":58,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":4},"100618156","effects-of-vibration-and-breathing-exercises-on-pain-and-anxiety-during-chest-tube-removal-100618156","NCT07327957","Effects of Vibration and Breathing Exercises on Pain and Anxiety During Chest Tube Removal","The Effect of Vibration and Breathing Exercises Applied Before Chest Tube Removal on Pain and Anxiety: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Adult patients aged 18 years and older\n* Hospitalized patients with an indwelling chest tube scheduled for removal\n* First-time chest tube placement\n* Conscious, oriented, and cooperative\n* Able to understand and communicate in Turkish\n* Hemodynamically stable at the time of chest tube removal\n* No use of analgesic or sedative medications within 4 hours prior to the procedure\n* Willing and able to provide written informed consent\n\nExclusion Criteria:\n\n* History of any cognitive or psychiatric disorder\n* Previous experience with chest tube placement\n* Requirement for mechanical ventilation or endotracheal intubation\n* Presence of chronic pain or regular use of analgesic medications\n* Use of analgesic or sedative medications immediately before chest tube removal\n* Unstable clinical condition at the time of the procedure\n* Refusal or inability to provide informed consent","65 Years",{"count":55,"type":21},70,[24],"Removing a chest tube is a common procedure after chest surgery, but it can cause significant pain and anxiety for patients. Although medications can help reduce these symptoms, they may have side effects and are not always sufficient. Therefore, simple and safe non-drug methods are increasingly used to improve patient comfort.\n\nThis randomized controlled study aims to examine the effects of vibration and breathing exercises applied before chest tube removal on patients' pain and anxiety levels. Adult patients with a chest tube will be randomly assigned to one of three groups: a vibration group, a breathing exercise group, or a control group receiving standard care. Pain and anxiety levels will be measured before the procedure and after chest tube removal using validated scales.\n\nThe findings of this study are expected to show whether vibration and breathing exercises are effective in reducing pain and anxiety during chest tube removal. If effective, these methods may offer nurses an easy, low-cost, and safe way to improve patient comfort and support evidence-based nursing care.",[59,60,61],"Postoperative Pain","Anxiety","Thoracic Drainage","2026-01-08",{"date":64,"type":38},"2026-01-09",{"date":66,"type":21},"2025-12-31",{"date":68,"type":21},"2026-08-20",{"name":44,"class":45},{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":4,"eligibilityCriteria":76,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":53,"enrollmentInfo":77,"targetDuration":4,"studyType":22,"phases":78,"briefSummary":79,"conditions":80,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":87,"completionDateStruct":88,"leadSponsor":90,"locationsCount":4},"100611751","hologram-burn-dressing-on-pain-anxiety-fear-patient-satisfaction-and-physiological-parameters-100611751","NCT07244653","Hologram Burn Dressing on Pain, Anxiety, Fear, Patient Satisfaction, and Physiological Parameters","Effect of Hologram Application During Burn Dressing on Pain, Anxiety, Fear, Patient Satisfaction, and Physiological Parameters: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Between the ages of 18 and 65,\n* Able to read, write, and speak Turkish,\n* Not participating in any other clinical trials at the same time,\n* Patients who were decided to be admitted to a burn unit,\n* No infected cases,\n* Patients who did not undergo minor and\u002For major surgical procedures that could affect the wound healing process,\n* No chronic illness other than burns,\n* No cognitive, sensory, or other problems that would prevent verbal communication and understanding the information given,\n* Second-degree burn with a total body surface area (TBSA) of less than 20%; Patients were included in the study if their burn rate was below 15% (20% in Grade 2 patients; sedation was required in Grade 3 patients with burn rates above 15%),\n* 2nd and 3rd degree burns in the granulation stage (2nd and 3rd degree burns requiring granulation treatment and experiencing high pain),\n* No burns on the head, ears, or face,\n* Daily dressing changes with a frequency of 1-15 dressing changes,\n* No complaints that would prevent participation in the study, such as respiratory problems,\n* No vision or hearing problems.\n\nExclusion Criteria:\n\n* Those with a pain intensity between 8 and 10 points (sedation is required when the pain intensity is 8 or higher),\n* Those under the influence of various non-pharmacological treatment methods that may affect pain,\n* Patients requiring advanced surgical procedures such as fasciotomy, escharotomy, or amputation,\n* Patients receiving sedation during the dressing,\n* Patients interrupting the hologram video during the dressing,\n* First-degree burns,\n* Those with neurological, psychological, or psychiatric illnesses,\n* Patients receiving sedation during the dressing,\n* Patients interrupting the hologram video during the dressing",{"count":55,"type":21},[24],"Burn injuries are a significant global health problem, leading to serious physical, psychological, and social challenges for affected individuals. The literature emphasizes that dressing changes are among the most painful and anxiety-provoking procedures, negatively impacting treatment adherence and patient well-being. Although pharmacological methods are used to alleviate pain and anxiety, they are often insufficient due to potential side effects and addiction risks.\n\nIn recent years, advancements in digital technologies-particularly virtual reality (VR), augmented reality (AR), and hologram applications-have offered promising distraction-based approaches. Hologram technology, through three-dimensional and interactive visuals, can divert the patient's attention from traumatic stimuli, thereby reducing pain, anxiety, and fear in an innovative way. However, there is limited scientific evidence regarding the use of hologram applications during burn dressing changes.\n\nThis study aims to examine the effects of hologram applications on pain, anxiety, fear, patient satisfaction, and physiological parameters during burn dressing procedures. The research will be conducted at Erzurum City Hospital Burn Center, with a total of 70 patients assigned to experimental and control groups using simple randomization. Data collection tools will include the Visual Analogue Scale (VAS), the State-Trait Anxiety Inventory (STAI), the Burn Specific Pain Anxiety Scale, satisfaction and fear VAS assessments, and physiological parameter recording forms. The study will be carried out between November 2025 and May 2026. The results are expected to provide evidence-based insights into the feasibility and effectiveness of hologram technology as a non-pharmacological, innovative intervention in burn care.",[60,81,82,83],"Burn Pain","Burn Patients","Fear","2025-12-26",{"date":86,"type":38},"2025-12-29",{"date":66,"type":21},{"date":89,"type":21},"2026-07-20",{"name":44,"class":45},""]