[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"nursing-care\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:nursing-care":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,15,0,[8,49,84,117,147,176,203,229,250,275,310,334,357,382,413],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":30,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100644112","effect-of-ai-assisted-respiratory-training-on-pain-fatigue-and-respiratory-parameters-in-patients-after-open-heart-surgery-100644112",false,"NCT07665593","Effect of AI-Assisted Respiratory Training on Pain, Fatigue and Respiratory Parameters in Patients After Open Heart Surgery","The Effect of Artificial Intelligence-Assisted Respiratory Training on Pain, Fatigue and Respiratory Parameters in Patients After Open Heart Surgery","Inclusion Criteria:\n\n* Patients undergoing elective open heart surgery.\n* Conscious.\n* Speaks and understands Turkish.\n* Has a chest tube inserted (on the right and\u002For left side).\n* No visual, auditory, or mental problems.\n* Willing to participate in the study.\n\nExclusion Criteria:\n\n* Undergoing concurrent other chest surgery or having a history of re-surgery.\n* Development of early postoperative complications (e.g., atelectasis) within 0-3 days.\n* Any loss of an extremity.\n* Long-term immobilization and intubation.\n* Development of severe post-surgery infections (such as mediastinitis or sepsis) or respiratory complications (such as pneumonia or atelectasis).","ALL","18 Years",{"count":19,"type":20},111,"ESTIMATED","INTERVENTIONAL",[23],"NA","This randomized controlled study aims to evaluate the effect of artificial intelligence (AI)-assisted respiratory training on fatigue, pain, and respiratory parameters in patients after open heart surgery.",[26,27,28,29],"Nursing Care","Pain","Breathing Exercises","Fatigue Recovery",[31,32,33,34,35],"pain","nursing care","fatigue","breathing exercises","open heart surgery","RECRUITING","2026-06-22",{"date":39,"type":40},"2026-06-24","ACTUAL",{"date":42,"type":40},"2026-02-10",{"date":44,"type":20},"2026-10",{"name":46,"class":47},"Kocaeli University","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":56,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":21,"phases":59,"briefSummary":60,"conditions":61,"keywords":69,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":4},"100642365","caregiver-training-regarding-percutaneous-endoscopic-gastrostomy-feeding-and-care-100642365","NCT07647185","Caregiver Training Regarding Percutaneous Endoscopic Gastrostomy Feeding and Care","Effects of Caregiver Training on Stress, Knowledge, and Skill Level Regarding Percutaneous Endoscopic Gastrostomy Care","Inclusion Criteria:\n\n* Being 18 years of age or older\n* Being the patient's primary caregiver (the person who regularly provides daily PEG care and nutrition)\n* Being literate\n* Being proficient in communicating in Turkish (understanding and expressing oneself)\n* Volunteering to participate in the study and providing written informed consent\n* The caregiver must not have a diagnosed psychiatric illness requiring active treatment\n\nExclusion Criteria:\n\n* Being under 18 years of age\n* Being illiterate\n* Not being proficient in communicating in Turkish\n* Not giving written informed consent to participate in the study\n* Having a diagnosed psychiatric illness requiring active treatment",true,{"count":58,"type":20},54,[23],"Background: Percutaneous endoscopic gastrostomy (PEG) is used for patients who cannot be fed orally, have a reduced swallowing reflex, or require long-term feeding. PEG care and feeding, which is performed with nursing support in healthcare institutions, becomes the responsibility of the caregiver after discharge. During this process, a lack of information and insufficient mastery of PEG feeding can create stress for caregivers. This situation jeopardizes patient safety. Therefore, healthcare professionals should manage patient-centered care from the moment the PEG indication is established until discharge. In this regard, consistent guidance and healthcare education are needed for caregivers.\n\nAim and hypotheses: This study aims to examine the effects of hands-on PEG feeding and PEG care training, enriched with audiovisual materials (video), on caregivers' knowledge level, skills, and stress levels related to the PEG feeding and care process.\n\nH1: The training provided for caregivers increases their knowledge level regarding PEG feeding and care.\n\nH2: The training provided for caregivers increases their skill level regarding PEG feeding and care.\n\nH3: The training provided for caregivers reduces their stress levels related to PEG feeding and care.\n\nDesign: This study was designed as a randomized controlled trial with experimental and control groups.\n\nMethod: The study population will consist of caregivers of patients receiving inpatient care at a state hospital and undergoing PEG placement for the first time. The sample size was calculated using the G-Power 3.1 program, resulting in a sample size of 54 (n1=27, n2=27), including the dropout rate. Participants will be randomly assigned to groups. The intervention group will receive hands-on training related to PEG feding and care using a low-fidelity model. In addition, caregivers will be provided with video training on PEG feeding and care that they can watch for review when needed. The control group will receive standard institutional training provided by the nutrition nurse of the institution where the study is conducted. Data will be collected face-to-face using a \"Personal Information Form\", \"State Anxiety Inventory\", \"Skills Checklist\", and \"PEG Care Konowledge Form\". Three measurements will be taken in the study. Test 0: Before the training (Personal Information Form, State Anxiety Inventory), Test 1: After the training (with the PEG Care Knowledge Form and the State Anxiety Inventory). Additionally, the researcher will evaluate the caregiver's feeding and care practices using the Skills Checklist. Test 2: Two weeks after from the Test 1 (State Anxiety Inventory and PEG Care Konowledge Form), also the researcher will also evaluate the caregiver's practices a second time using the Skills Checklist. Data will be analyzed using the SPSS Statistics 27 software package.",[62,63,64,65,26,66,67,68],"Caregiver","Caregiver Anxiety","Simulation Training","State Anxiety","Video-Assisted","Percutaneous Endoscopic Gastrostomy (PEG)","Training",[70,71,64,72,73],"Nursing","Caregivers","Anxiety","Gastrostomy","NOT_YET_RECRUITING","2026-06-09",{"date":77,"type":40},"2026-06-15",{"date":79,"type":20},"2026-08-01",{"date":81,"type":20},"2027-03-30",{"name":83,"class":47},"Duzce University",{"id":85,"slug":86,"hasResults":11,"nctId":87,"briefTitle":88,"officialTitle":89,"acronym":90,"eligibilityCriteria":91,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":92,"targetDuration":4,"studyType":21,"phases":94,"briefSummary":95,"conditions":96,"keywords":100,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":108,"lastUpdatePostDateStruct":109,"startDateStruct":111,"completionDateStruct":113,"leadSponsor":115,"locationsCount":48},"100639783","nursing-intervention-for-adaptation-after-myocardial-revascularization-100639783","NCT07576569","Nursing Intervention for Adaptation After Myocardial Revascularization","Preliminary Effectiveness of a Nursing Intervention Aimed at Improving Adaptation in Patients and Their Caregivers During the Outpatient Postoperative Period Following Myocardial Revascularization","ADAPT-CABG","Inclusion Criteria:\n\n* Adults aged 18 years or older who have undergone myocardial revascularization surgery, completed the immediate postoperative in-hospital period without major complications, and have been discharged for outpatient management according to institutional protocols\n* Patients who, at the time of discharge, do not require ventilatory support, invasive hemodynamic support, or continuous monitoring, and present documented clinical stability\n* Presence of an identified primary caregiver actively involved in the home care process during the outpatient postoperative period\n* Preserved cognitive capacity in both patient and caregiver, allowing understanding of instructions, participation in the intervention, and completion of assessment instruments\n* Written informed consent provided by both patient and caregiver\n\nExclusion Criteria:\n\n* Patients presenting severe postoperative complications, such as deep surgical site infection, persistent hemodynamic instability, major neurological events, or readmission to the intensive care unit at the start of the intervention Patients with moderate to severe cognitive impairment, decompensated psychiatric disorders, or neurological conditions that limit understanding, communication, or active participation\n* Caregivers with physical, cognitive, or emotional limitations that compromise the effective performance of the caregiving role during the follow-up period\n* Patients without a clearly identified support network or without an available primary caregiver to participate in the study\n* Concurrent participation in other clinical, educational, or psychosocial intervention studies that may interfere with the proposed intervention\n* Language or cultural barriers that prevent understanding of the intervention content or interaction with the research team, without adequate mediation",{"count":93,"type":20},40,[23],"Introduction: Myocardial revascularization is an essential procedure for patients with cardiovascular disease. Its recovery in the outpatient setting involves significant challenges for both the patient and the caregiver. This recovery phase may generate physical, emotional, and psychological complications that require an effective adaptation process of the patient-caregiver dyad to ensure successful recovery and improved quality of life.\n\nObjective: To evaluate the preliminary effectiveness of a nursing intervention aimed at improving adaptation in the patient-caregiver dyad during the outpatient postoperative period following myocardial revascularization, compared with usual care, in Bucaramanga during the period 2026-2027.\n\nMaterials and Methods: A pilot randomized controlled trial will be conducted to develop and evaluate a novel nursing intervention aimed at promoting adaptation in patients undergoing outpatient postoperative myocardial revascularization and their caregivers. The intervention will be designed and its feasibility, acceptability, and preliminary effectiveness will be assessed. Data analysis will be performed using descriptive and inferential statistical methods, considering the distribution and behavior of the data.\n\nExpected Results: The study is expected to assess the preliminary effectiveness of the proposed intervention through the integration of theoretical and empirical components.",[97,98,99,26],"Coronary Artery Disease","Myocardial Revascularization","Postoperative Recovery After Cardiac Surgery",[98,101,102,103,104,105,106,107],"Nursing Intervention","Patient-Caregiver Dyad","Adaptation","Postoperative Recovery","Cardiovascular Disease","Randomized Controlled Trial","Outpatient Care","2026-05-02",{"date":110,"type":40},"2026-05-08",{"date":112,"type":20},"2027-01",{"date":114,"type":20},"2027-12",{"name":116,"class":47},"Universidad de la Sabana",{"id":118,"slug":119,"hasResults":11,"nctId":120,"briefTitle":121,"officialTitle":122,"acronym":4,"eligibilityCriteria":123,"healthyVolunteers":11,"sex":16,"minAge":124,"maxAge":125,"enrollmentInfo":126,"targetDuration":4,"studyType":21,"phases":128,"briefSummary":129,"conditions":130,"keywords":132,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":138,"lastUpdatePostDateStruct":139,"startDateStruct":141,"completionDateStruct":143,"leadSponsor":145,"locationsCount":48},"100632635","effects-of-cartoons--interactive-storytelling-on-fear-and-comfort-in-6-9-year-olds-during-nebulizer-treatment-100632635","NCT07516249","Effects of Cartoons & Interactive Storytelling on Fear and Comfort in 6-9 Year Olds During Nebulizer Treatment","The Effect of Cartoon Viewing and Breath-Synchronized Interactive Storytelling During Nebulizer Medication Administration on Fear, Emotional Behavior, and Comfort in 6-9 Year Old Children: A Randomized Controlled Study","Inclusion Criteria:\n\n* \\- Children aged 6-9 years\n* Scheduled to receive nebulizer inhalation therapy due to acute or chronic respiratory disease\n* Conscious, responsive to environmental stimuli, and able to communicate verbally or nonverbally\n* Without a diagnosed neurodevelopmental disorder (severe autism spectrum disorder, severe intellectual disability, etc.)\n* Without severe hearing or vision loss that would impair storytelling and visual material comprehension\n* Without signs of respiratory failure requiring emergency intervention during nebulizer administration\n* With written informed consent from a parent or legal guardian\n* Children who are willing to participate in the study after being given explanations appropriate to their age and developmental level.\n\nExclusion Criteria:\n\n* Patients who require emergency medical intervention during nebulizer application, such as severe respiratory distress, cyanosis, or significantly low oxygen saturation.\n* Patients who are unconscious or unable to respond adequately to environmental stimuli.","6 Years","9 Years",{"count":127,"type":20},96,[23],"Fear and anxiety experienced by children during inhalation therapy (using a nebulizer or vaporizer) are key factors that make treatment compliance difficult and reduce the quality of care. Young children, in particular, may perceive this process as \"threatening\" due to mask use, the noise produced by the device, and a sense of loss of control. This situation triggers a significant physiological stress response in the child.\n\nTherefore, in pediatric nursing, non-pharmacological methods that increase children's participation in treatment are of great importance. The literature indicates that interventions such as showing cartoons, playing music, and using distracting visual materials both reduce anxiety and improve stress indicators like heart rate. Additionally, therapeutic play has been proven to help children adapt to the hospital environment and soothe their emotional reactions.\n\nThis study aims to evaluate the effectiveness of a nursing intervention-designed to enhance children's physical comfort and manage their fear and anxiety during inhalation therapy-that is breath-synchronized, interactive, and story-based.",[131,26],"Distraction Methods",[133,134,135,136,137],"Administration, Inhalation","Distraction methods","fear","comfort","cartoon","2026-04-02",{"date":140,"type":40},"2026-04-07",{"date":142,"type":20},"2026-04-23",{"date":144,"type":20},"2026-10-30",{"name":146,"class":47},"Mersin University",{"id":148,"slug":149,"hasResults":11,"nctId":150,"briefTitle":151,"officialTitle":152,"acronym":153,"eligibilityCriteria":154,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":155,"targetDuration":4,"studyType":157,"phases":4,"briefSummary":158,"conditions":159,"keywords":163,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":167,"lastUpdatePostDateStruct":168,"startDateStruct":170,"completionDateStruct":172,"leadSponsor":174,"locationsCount":48},"100629200","patient-satisfaction-study-at-aou-maggiore-della-carit-score-100629200","NCT07471581","Patient Satisfaction Study at AOU Maggiore Della Carità (SCORE)","Patient Satisfaction With Care: A Cross-Sectional Observational Study at AOU Maggiore Della Carità, Novara (SCORE)","SCORE","Inclusion Criteria:\n\n* Adult inpatients (age ≥ 18 years) admitted to ordinary wards of AOU Maggiore della Carità.\n* Hospitalization for at least 48 hours at the time of questionnaire administration.\n* Able to provide informed consent.\n* Able to understand and speak Italian.\n\nExclusion Criteria:\n\n* Hospitalization shorter than 48 hours.\n* Age \\\u003C 18 years.\n* Cognitive impairment or clinical conditions preventing comprehension or autonomous completion of the questionnaire.\n* Refusal or inability to provide informed consent.",{"count":156,"type":20},250,"OBSERVATIONAL","The general aim of this study is to assess and analyze the level of patient satisfaction with nursing care among inpatients in the ordinary wards of the AOU Maggiore della Carità in Novara (Italy). Using the validated Newcastle Satisfaction with Nursing Scales (NSNS), the study intends to produce reliable and comparable data that reflect patients' perceived quality of care across multiple dimensions, including relationships, emotional support, information, and time devoted by nurses. The study aims to provide an updated overview of patient experiences, identifying strengths and areas for improvement. These results will offer guidance for organizational and educational strategies to promote more personalized, human-centered nursing care aligned with international quality and safety recommendations, without altering routine clinical practice.",[160,70,26,161,162],"Patient Satisfaction","Patient-Centered Care","Cross-Sectional Studies",[160,70,26,161,164,165,166],"Cross-Sectional Study","Healthcare Quality","Patient Experience","2026-03-10",{"date":169,"type":40},"2026-03-13",{"date":171,"type":20},"2026-04-09",{"date":173,"type":20},"2026-05-31",{"name":175,"class":47},"Università degli Studi del Piemonte Orientale Amedeo Avogadro",{"id":177,"slug":178,"hasResults":11,"nctId":179,"briefTitle":180,"officialTitle":180,"acronym":4,"eligibilityCriteria":181,"healthyVolunteers":11,"sex":16,"minAge":182,"maxAge":4,"enrollmentInfo":183,"targetDuration":4,"studyType":21,"phases":185,"briefSummary":186,"conditions":187,"keywords":190,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":195,"lastUpdatePostDateStruct":196,"startDateStruct":198,"completionDateStruct":200,"leadSponsor":201,"locationsCount":48},"100598388","effects-of-two-different-eye-care-practices-on-eye-complications-in-mechanically-ventilated-intensive-care-patients-100598388","NCT07070843","Effects of Two Different Eye Care Practices on Eye Complications in Mechanically Ventilated Intensive Care Patients","Inclusion Criteria:\n\n* Age 18 years or older\n* Receiving mechanical ventilation\n* Glasgow Coma Scale (GCS) score \\\u003C 12\n* At least 24 hours have passed since ICU admission\n* Baseline Schirmer test result indicating tear production \\> 5 mm prior to study inclusion\n\nExclusion Criteria:\n\n* Diagnosed with brain death\n* Presence of facial or ocular trauma\n* Patients with head trauma\n* Patients who have undergone brain surgery\n* Patients diagnosed with an eye infection or chemosis\n\nWithdrawal Criteria:\n\n* Patient's death during the study period\n* Extubation of the patient before completion of the care period","18 Days",{"count":184,"type":20},156,[23],"This study was designed as a prospective, randomized controlled experimental study aiming to compare different approaches to eye care in intensive care patients receiving mechanical ventilation. In this study, patients receiving mechanical ventilation in the intensive care unit will be randomly assigned to four groups using a simple randomization method:\n\n1. Control Group: Standard Eye Care\n2. Intervention Group 1: Eye Care with Eye Care Kit\n3. Intervention Group 2: Eye Care According to Eye Care Protocol\n4. Intervention Group 3: Eye Care with Both Protocol and Eye Care Kit Research Hypotheses H1: Eye care provided using a care protocol is more effective in preventing the development of complications compared to standard eye care.\n\nH2: Eye care provided using an eye care kit is more effective in preventing the development of ocular complications compared to standard eye care.\n\nH3: The combined use of an eye care kit and a care protocol is more effective in preventing the development of ocular complications compared to using the care protocol alone.\n\nH4: The use of an eye care kit is more effective in preventing the development of ocular complications compared to the use of a care protocol.",[188,26,189],"Eye Care","Intensive Care Unit",[191,192,193,194],"Critical care nursing","Eye infections","Intensive care units","Nursing care","2026-01-27",{"date":197,"type":40},"2026-01-29",{"date":199,"type":40},"2025-07-01",{"date":44,"type":20},{"name":202,"class":47},"Istanbul Saglik Bilimleri University",{"id":204,"slug":205,"hasResults":11,"nctId":206,"briefTitle":207,"officialTitle":208,"acronym":4,"eligibilityCriteria":209,"healthyVolunteers":56,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":210,"targetDuration":4,"studyType":21,"phases":212,"briefSummary":213,"conditions":214,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":220,"lastUpdatePostDateStruct":221,"startDateStruct":223,"completionDateStruct":225,"leadSponsor":227,"locationsCount":48},"100610591","the-effectiveness-of-serious-game-based-training-for-nursing-students-in-postpartum-haemorrhage-management-100610591","NCT07229573","The Effectiveness of Serious Game-Based Training for Nursing Students in Postpartum Haemorrhage Management","The Effectiveness of Serious Game-Based Training for Nursing Students in Postpartum Haemorrhage Management: A Randomised Controlled Trial","Inclusion Criteria:\n\na) Third-year nursing students taking the Obstetrics and Gynaecology Nursing course, b) Not experiencing any verbal or written communication problems, c) Not being an exchange student, d) Being willing to provide written consent before participating in the study.\n\nExclusion Criteria:\n\nNot meeting the inclusion criteria",{"count":211,"type":20},70,[23],"This randomised controlled trial aims to evaluate the effectiveness of serious game-based training for postpartum haemorrhage (PPH) management among third-year nursing students. The study employs a pre-test-post-test design with two parallel groups: an experimental group (game-based education) and a control group (traditional education). The sample size was determined by power analysis to be 70 students in total, with 35 students in each group. Participants will be assigned in a 1:1 ratio by computer-assisted block randomisation by a person independent of the research team; students and instructors will not be blinded, but the biostatistician performing the data analysis will be blinded. The intervention group will first receive traditional education, followed by gamification-based education including nursing interventions in the management of PPB; the control group will receive only traditional education. Data will be collected using the PPK Management Knowledge and Skills Assessment Form and the PPK Management Self-Confidence Scale.",[215,216,217,218,219,26],"Gamification","Gamification in Health Education","Nurse Education","Nursing Students","Postpartum Hemorrhage","2025-11-13",{"date":222,"type":40},"2025-11-17",{"date":224,"type":40},"2025-11-05",{"date":226,"type":20},"2025-12-30",{"name":228,"class":47},"Sakarya University",{"id":230,"slug":231,"hasResults":11,"nctId":232,"briefTitle":233,"officialTitle":233,"acronym":4,"eligibilityCriteria":234,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":235,"targetDuration":4,"studyType":21,"phases":237,"briefSummary":238,"conditions":239,"keywords":4,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":241,"lastUpdatePostDateStruct":242,"startDateStruct":244,"completionDateStruct":246,"leadSponsor":248,"locationsCount":4},"100587502","the-effect-of-bedside-whiteboard-use-on-anxiety-depression-and-nursing-care-in-chronic-obstructive-pulmonary-patients-100587502","NCT06929221","The Effect of Bedside Whiteboard Use on Anxiety, Depression and Nursing Care in Chronic Obstructive Pulmonary Patients","Inclusion Criteria:\n\n* 18 years of age or older\n* Having a medical diagnosis of COPD\n* To be in a condition to be followed up with at least 7 days\n\nExclusion Criteria:\n\n* \\- Having strong reading and comprehension skills",{"count":236,"type":20},128,[23],"ABSTRACT Chronic obstructive pulmonary disease (COPD) is a disease characterized by the inability of the body to adequately exchange gases, resulting in progressive shortness of breath that can form secretions and compromise the performance of daily activities. COPD is reported as the third most common cause of death worldwide, with 3.23 million deaths in 2019. Anxiety and depression are common in individuals with COPD. However, COPD is more common in patients with other chronic diseases such as hypertension, diabetes, cancer or musculoskeletal disorders. Communication is a key component in interprofessional care as well as in improving patient care outcomes. Strategies to address gaps in the quality of information and communication between patients, caregivers and professionals improve patient safety as well as quality of care. One of these strategies is the use of whiteboards at the bedside. The use of whiteboards at the bedside has emerged as a strategy to improve interprofessional team participation, communication and information sharing with care teams, patients and families. This study will be conducted in randomized controlled single blind parallel groups to examine the effect of bedside whiteboard use on anxiety, depression and nursing care satisfaction in COPD patients. The research will consist of patients who are hospitalized in Atatürk University Research Hospital Chest Diseases Clinic and who meet the inclusion criteria. In the results of the research, it is thought that the use of whiteboard will affect the communication between health care team members.",[240,26],"COPD","2025-09-30",{"date":243,"type":40},"2025-10-01",{"date":245,"type":20},"2025-12-15",{"date":247,"type":20},"2026-07-15",{"name":249,"class":47},"Agri Ibrahim Cecen University",{"id":251,"slug":252,"hasResults":11,"nctId":253,"briefTitle":254,"officialTitle":255,"acronym":4,"eligibilityCriteria":256,"healthyVolunteers":56,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":257,"targetDuration":4,"studyType":21,"phases":259,"briefSummary":260,"conditions":261,"keywords":4,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":266,"lastUpdatePostDateStruct":267,"startDateStruct":269,"completionDateStruct":271,"leadSponsor":273,"locationsCount":4},"100603602","effect-of-the-aspiration-care-bundle-on-preventing-vap-100603602","NCT07138651","Effect of the Aspiration Care Bundle on Preventing VAP","Yoğun Bakım Hastalarına Uygulanan Aspirasyon Bakım Paketinin Ventilatör İlişkili Pnömoni Gelişimini Önlemeye Etkisi: Yarı Deneysel Çalışma","Inclusion Criteria:\n\n* Patients admitted to the pulmonary intensive care unit\n* Aged 18 years or older\n* Connected to mechanical ventilation via ETT\u002FTT\n* Glasgow Coma Scale score: 8 or higher\n* Remaining in the intensive care unit for at least 24 hours\n* Patients who have not previously been diagnosed with ventilator-associated pneumonia will be included in the study.\n\nExclusion Criteria:\n\n* Transferred from the pulmonary intensive care unit to another clinic\n* Diagnosed with ventilator-associated pneumonia within the first 24 hours\n* Glasgow Coma Scale score fell below 8 during the study\n* Deceased at the time of data collection\n* Patients who developed any complications related to aspiration (atelectasis, hypoxemia, bradypnea, etc.) prior to the study will be excluded from the study.",{"count":258,"type":20},60,[23],"Many pharmacological and non-pharmacological interventions are used to prevent ventilator-associated pneumonia (VAP). Nurses are directly responsible for implementing non-pharmacological interventions and therefore have an important role in preventing VAP. The most important non-pharmacological nursing interventions to prevent VAP are hand hygiene and oral care. In addition, the head of the bed should be elevated to 30°-45°, head pressure should be monitored, and subglottic aspiration should be performed. Various care packages have been developed to prevent VAP. It has been determined that these care packages reduce the incidence of VAP. The aim of this study was to investigate the effect of the aspiration care package applied in the intensive care unit on preventing the development of ventilator-associated pneumonia, and it was planned as a quasi-experimental study.",[262,263,264,265,26],"VAP - Ventilator Associated Pneumonia","Care","Bundle Care","Aspiration","2025-08-23",{"date":268,"type":40},"2025-08-29",{"date":270,"type":20},"2025-09-15",{"date":272,"type":20},"2026-09-15",{"name":274,"class":47},"Akdeniz University",{"id":276,"slug":277,"hasResults":11,"nctId":278,"briefTitle":279,"officialTitle":280,"acronym":281,"eligibilityCriteria":282,"healthyVolunteers":56,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":283,"targetDuration":4,"studyType":21,"phases":285,"briefSummary":286,"conditions":287,"keywords":295,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":301,"lastUpdatePostDateStruct":302,"startDateStruct":304,"completionDateStruct":306,"leadSponsor":308,"locationsCount":48},"100593588","high-sensitivity-troponin-i-in-addition-to-guideline-based-care-in-ems-100593588","NCT07008391","High-Sensitivity Troponin I in Addition to Guideline-Based Care in EMS","High-Sensitivity Troponin I in Addition to Guideline-Based Care in Emergency Medical Service - an Open Randomized Controlled Trial","TIGER","Inclusion Criteria:\n\n* Chestpain \u002F discomfort and\u002For\n* Clinical suspicion of myocardial infarction by the prehospital personeel\n\nExclusion Criteria:\n\n* Patients suffering from a trauma and conveyed to the trauma level 1 hospital.\n* Missing valid social security number\n* Not beeing able to give informed consent\n* Not a primary assignment",{"count":284,"type":20},1419,[23],"The TIGER study is a study investigating the utlility of a point-of-care blood analyse of Troponin I to help identify patients with heart attacks in the prehospital emergency care. The study is conducted within the ambulance services of Region Stockholm and compares standard medical care with and without the addition of this quick test.\n\nChest pain is one of the most common reasons for ambulance dispatch, but currently only about one-third of heart attacks are detected before arriving at the hospital-mainly through ECG. The remaining two-thirds are not identified until after further testing at the emergency department. The TIGER study aims to improve early diagnosis by using a high-sensitivity, point-of-care Troponin I test already in the prehospital phase.\n\nThe study is a randomized controlled trial, where participants are randomly assigned to one of two groups. One group receives standard emergency care along with the rapid Troponin I test in the ambulance. The other group receives standard care without the test. The goal is to evaluate whether the use of Troponin I testing leads to faster and more accurate identification of heart attacks, ultimately improving patient outcomes.\n\nIn total, about 1,419 adult patients with chest pain or suspected heart attack will participate. The primary outcome being measured is the time from first medical contact to PCI (balloon angioplasty). Secondary outcomes include time spent in different parts of care, hospital length of stay, the occurrence of serious events (such as heart attack, stroke, or death), and the diagnostic accuracy of the test.\n\nThe study has been approved by the Swedish Ethical Review Authority and includes safety monitoring through an interim analysis after the first 150 patients. Test results from the Troponin I analysis are clearly marked as part of the research study and should be interpreted by the responsible physician alongside other clinical findings.",[288,26,289,290,291,292,293,294],"Emergency Medical Services","Cardiology","Myocardial Infarction","Myocardial Infarction or Chest Pain","Myocardial Infarction, Acute","Emergencies","Ambulance",[294,296,297,298,299,300],"Prehospital emergency nurse","Sweden","Point-of-care","troponin","high sensitive troponin","2025-06-27",{"date":303,"type":40},"2025-07-02",{"date":305,"type":40},"2025-06-25",{"date":307,"type":20},"2026-12-30",{"name":309,"class":47},"Karolinska Institutet",{"id":311,"slug":312,"hasResults":11,"nctId":313,"briefTitle":314,"officialTitle":315,"acronym":4,"eligibilityCriteria":316,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":317,"targetDuration":4,"studyType":21,"phases":318,"briefSummary":319,"conditions":320,"keywords":323,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":327,"lastUpdatePostDateStruct":328,"startDateStruct":329,"completionDateStruct":331,"leadSponsor":332,"locationsCount":4},"100596383","information-on-the-use-of-anti-embolic-stockings-in-patients-undergoing-vein-surgery-100596383","NCT07044739","Information on the Use of Anti-embolic Stockings in Patients Undergoing Vein Surgery","The Effect of Information on the Use of Anti-embolic Stockings on Discharge Readiness and Satisfaction With Nursing Care in Patients Undergoing Vein Surgery","Inclusion Criteria:\n\n• Having had vein surgery\n\nExclusion Criteria:\n\n* Having hearing\u002Fvision\u002Fmental problems\n* Having been diagnosed with a psychological illness (schizophrenia, depression)\n* Having any of the contraindications for the use of anti-embolic stockings in the patient (the patient has peripheral arterial disease or bypass grafts, peripheral neuropathy or other causes of sensory impairment, heart failure, pulmonary or leg edema, poor skin condition due to dermatitis\u002Fdiabetes\u002Fvenous ulcers, allergy or sensitivity to the materials in the stockings, and leg deformities that prevent the stockings from fitting properly)",{"count":258,"type":20},[23],"The aim of this study was to investigate the effect of information given to patients undergoing vein surgery regarding the use of anti-embolic stockings on their readiness for discharge and satisfaction with nursing care.",[26,321,322],"Vascular Surgery","Patient Education",[32,324,325,326],"vascular surgery","discharge","postoperative period","2025-06-26",{"date":199,"type":40},{"date":330,"type":20},"2025-08-15",{"date":77,"type":20},{"name":333,"class":47},"Aydin Adnan Menderes University",{"id":335,"slug":336,"hasResults":11,"nctId":337,"briefTitle":338,"officialTitle":339,"acronym":4,"eligibilityCriteria":340,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":341,"targetDuration":4,"studyType":21,"phases":342,"briefSummary":343,"conditions":344,"keywords":4,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":348,"lastUpdatePostDateStruct":349,"startDateStruct":351,"completionDateStruct":353,"leadSponsor":355,"locationsCount":4},"100591898","effect-of-earplugs-and-eye-masks-used-after-orthopedic-surgery-on-comfort-and-quality-of-recovery-100591898","NCT06986408","Effect of Earplugs and Eye Masks Used After Orthopedic Surgery on Comfort and Quality of Recovery","Effect of Earplugs and Eye Masks Used After Orthopedic Surgery on Comfort and Quality of Recovery: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Patients who can speak and understand Turkish,\n* At least 18 years old,\n* No hearing impairment and not using hearing aids,\n* No psychiatric diagnosis and not using psychiatric medication regularly,\n* Patients who agree to participate in the study and have given written consent.\n\nExclusion Criteria:\n\n* Patients who do not agree to participate in the study and for whom written consent was not obtained.",{"count":258,"type":20},[23],"This research will be conducted as a randomized controlled trial to determine the effects of earplugs and eye masks used after orthopedic surgery on comfort and quality of recovery. This study is a single-center, parallel-group, open-label, randomized controlled clinical trial. This study will be conducted with 60 patients who underwent orthopedic surgery between June 2025 and October 2025. Participants will be randomized into two equal groups as the intervention group (n=30) and the control group (n=30). The patients in the experimental group will be administered the \"Informed Consent Form\" and the \"Patient Introduction Form\" after obtaining permission before surgery. Patients will be given an eye mask and earplugs on the nights following surgery and will be ensured to use them correctly. The \"General Comfort Scale\" and the \"Quality of Recovery Questionnaire (Qor-40)\" will be administered 24 and 48 hours after surgery. The patients in the control group will also be administered the \"Informed Consent Form\" and the \"Patient Introduction Form\" after obtaining permission before surgery. The \"General Comfort Scale\" and the \"Quality of Recovery Questionnaire (Qor-40)\" will be administered 24 and 48 hours after surgery. At the end of the study, the difference between the groups will be evaluated. In the analysis of this study, descriptive statistics, Shapiro-Wilk test, Chi-square test, t-test in independent groups, ANOVA test in repeated measures will be used.\n\nThe main questions it aims to answer:\n\nDo earplugs and eye masks used after orthopedic surgery have an effect on comfort level? Do earplugs and eye masks used after orthopedic surgery have an effect on the quality of recovery?",[345,26,346,347],"Orthopedic Surgery","Quality of Recovery 40","Comfort","2025-05-21",{"date":350,"type":40},"2025-05-23",{"date":352,"type":20},"2025-06-01",{"date":354,"type":20},"2025-11-20",{"name":356,"class":47},"Ankara Yildirim Beyazıt University",{"id":358,"slug":359,"hasResults":11,"nctId":360,"briefTitle":361,"officialTitle":362,"acronym":4,"eligibilityCriteria":363,"healthyVolunteers":56,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":364,"targetDuration":4,"studyType":21,"phases":365,"briefSummary":366,"conditions":367,"keywords":371,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":373,"lastUpdatePostDateStruct":374,"startDateStruct":376,"completionDateStruct":378,"leadSponsor":380,"locationsCount":48},"100567305","the-effect-of-the-operating-room-environment-on-patients-experienced-with-virtual-reality-glasses-before-surgery-100567305","NCT06666465","The Effect of the Operating Room Environment on Patients Experienced With Virtual Reality Glasses Before Surgery","Operating Room Environment Experienced by Patients With Virtual Reality Glasses Before Surgery The Effect of Surgical Experience on the Level of Surgical Fear and Perceptions of Care","Inclusion Criteria:\n\n* Being 18 years or older\n* Agreeing to participate in the research\n* Having elective cholecystectomy surgery\n* Knowledge of Turkish and no communication barriers\n* Having surgery for the first time and not having seen the operating room environment\n\nExclusion Criteria:\n\n* Being 18 years of age or younger\n* Refusal to participate in the research\n* Having undergone surgery and having seen the operating room environment before Not knowing Turkish and having any communication barrier",{"count":258,"type":20},[23],"This study was planned as a randomized controlled experimental study with a pretest-posttest design to examine the effect of the operating room environment experience of preoperative patients using virtual reality glasses on the patients' preoperative surgical fear level and care perceptions.",[368,369,26,370],"Clinical Practice","Virtual Reality","Simulation",[372],"Clinical practice","2025-03-21",{"date":375,"type":40},"2025-03-24",{"date":377,"type":40},"2024-08-15",{"date":379,"type":20},"2025-12-20",{"name":381,"class":47},"Saglik Bilimleri Universitesi",{"id":383,"slug":384,"hasResults":11,"nctId":385,"briefTitle":386,"officialTitle":387,"acronym":388,"eligibilityCriteria":389,"healthyVolunteers":56,"sex":390,"minAge":17,"maxAge":391,"enrollmentInfo":392,"targetDuration":4,"studyType":21,"phases":394,"briefSummary":395,"conditions":396,"keywords":400,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":404,"lastUpdatePostDateStruct":405,"startDateStruct":407,"completionDateStruct":409,"leadSponsor":411,"locationsCount":48},"100572190","the-effect-of-augmented-reality-based-training-on-preeclampsia-case-100572190","NCT06730048","The Effect of Augmented Reality Based Training on Preeclampsia Case","The Effect of Augmented Reality Based Training on Preeclampsia Case on Nursing Students' Diagnosis and Intervention Planning Skills","preeclamside","Inclusion Criteria:\n\n* Continuing the course of Women's Health and Diseases Nursing,\n\n  * Volunteering to participate in the research,\n  * No physical or psychological health problems preventing the completion of the research forms.\n\nExclusion Criteria:\n\n* \\- Not watching the whole case given with virtual glasses,\n* Failure to attend class during the week of the preeclampsia lecture in the course syllabus.","FEMALE","45 Years",{"count":393,"type":20},84,[23],"However, no study has been found in the care of preeclampsia, which is highly effective on maternal and fetal health. Therefore, this study was planned to determine the effect of augmented reality-based training on the diagnosis and intervention planning skills of nursing students.",[397,26,398,399],"Preeclampsia","Pregnancy","Augmented Reality",[401,32,402,403],"preeclampsia","pregnancy","augmented reality","2024-12-08",{"date":406,"type":40},"2024-12-12",{"date":408,"type":20},"2024-12-20",{"date":410,"type":20},"2025-08-20",{"name":412,"class":47},"Inonu University",{"id":414,"slug":415,"hasResults":11,"nctId":416,"briefTitle":417,"officialTitle":418,"acronym":4,"eligibilityCriteria":419,"healthyVolunteers":56,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":420,"targetDuration":4,"studyType":21,"phases":421,"briefSummary":422,"conditions":423,"keywords":425,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":429,"lastUpdatePostDateStruct":430,"startDateStruct":432,"completionDateStruct":434,"leadSponsor":436,"locationsCount":48},"100569058","7e-model-in-nursing-education-100569058","NCT06689306","7E Model in Nursing Education","TEACHING CARE BEHAVIORS to NURSING STUDENTS WITHIN the 7E LEARNING MODEL: a RANDOMIZED CONTROLLED STUDY","Inclusion Criteria:\n\n* Being 18 years of age or older\n* Not having dealt with this topic before,\n* Being a second year nursing student\n* Being willing to participate in the study\n* Not having any communication barriers,\n* Not having a psychiatric illness diagnosis or treatment.\n\nExclusion Criteria:\n\n* The student is from upper grades and taking this course from lower grades\n* Being a foreign national\n* Not wanting to participate in the research",{"count":211,"type":20},[23],"This study aimed to examine the effects of teaching caring behaviors based on the 7E learning model on nursing students' course success, learning permanence, critical thinking skills and motivation levels.",[424,26],"Nursing Education",[70,32,426,427,428],"nursing education","human caring theory","7E model","2024-11-13",{"date":431,"type":40},"2024-11-14",{"date":433,"type":20},"2024-11-15",{"date":435,"type":20},"2025-06-15",{"name":437,"class":47},"Ataturk University"]