[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Fu Jen Catholic University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":452},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,17,0,[8,45,76,103,129,157,183,208,235,263,286,305,329,353,375,403,426],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100627330","comparing-ultrasonic-and-conventional-spirometry-in-chronic-respiratory-disease-100627330",false,"NCT07447232","Comparing Ultrasonic and Conventional Spirometry in Chronic Respiratory Disease","A Comparative Study of Ultrasonic and Conventional Spirometers in Patients With Chronic Respiratory Diseases","Inclusion Criteria:\n\n* Adults aged 18 to 80 years.\n* Diagnosed with a chronic respiratory disease (e.g., COPD, asthma, bronchiectasis, or interstitial lung disease).\n* Willing to follow the instructions for using the ultrasonic spirometer.\n* Clinically stable and able to understand the study purpose and procedures, and who provide informed consent.\n\nExclusion Criteria:\n\n* Individuals who, after explanation, are still unable to properly perform the ultrasonic spirometry procedure.\n* Individuals who, after explanation, refuse to participate in the study.\n* Patients with unstable vital signs.\n* Pregnant or suspected pregnant women.","ALL","18 Years","80 Years",{"count":20,"type":21},100,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study compares a handheld ultrasonic spirometer with a standard hospital spirometer in adults with chronic respiratory diseases. Each participant will complete lung function tests using both devices. The study aims to determine whether the ultrasonic device provides accurate and reliable measurements for use in clinical or home settings.",[27,28],"Chronic Obstructive Pulmonary Disease (COPD)","Spirometry",[27,28,30,31],"Ultrasonic Flow Sensor","Pulmonary Function Test","RECRUITING","2026-07-01",{"date":35,"type":36},"2026-07-02","ACTUAL",{"date":38,"type":36},"2026-06-29",{"date":40,"type":21},"2026-07-31",{"name":42,"class":43},"Fu Jen Catholic University","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":16,"minAge":52,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":22,"phases":56,"briefSummary":57,"conditions":58,"keywords":64,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":70,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":44},"100627161","effects-of-mobilization-using-a-powered-lower-limb-exoskeleton-with-prolonged-mechanical-ventilation-100627161","NCT07445035","Effects of Mobilization Using a Powered Lower-limb Exoskeleton With Prolonged Mechanical Ventilation","Physiological and Functional Adaptations Associated With Robot-assisted Lower-limb Activity in Ventilator-dependent Hospitalized Patients","Inclusion Criteria:\n\n* Able to maintain a seated position for at least 1 minute.\n* The participant or their legal representative is able to sign the informed consent form.\n\nExclusion Criteria:\n\n* Inability to follow instructions.\n* Intubation\u002Ftracheostomy prior to current admission.\n* Diagnosis of severe left heart failure.\n* Diagnosis of neuromuscular disorders.\n* Unable to stand.\n* Complete paralysis of the lower extremities.\n* Presence of unhealed ulcers in the lower extremities.\n* Deep vein thrombosis of the lower extremities.\n* Lower-limb amputation.\n* Severe hypertension\n* Severe cardiac conditions\n* Severe bilateral joint disorders\n* Severe pain while standing\n* Severe osteoporosis\n* Lower-limb fracture\n* Ongoing epileptic seizure","45 Years","65 Years",{"count":55,"type":21},30,[24],"This study aims to evaluate the effects of powered lower-limb exoskeleton-assisted training on lower limb strength, respiratory parameters, 28-day ventilator-free days, and length of hospital stay in patients with prolonged mechanical ventilation admitted to a Respiratory Care Center. The goal is to provide clinical evidence for integrating rehabilitation and respiratory care in this patient population.",[59,60,61,62,63],"Prolonged Mechanical Ventilation","Ventilator Weaning","Ventilator Dependent","Exoskeleton Device","Exercise Training",[65,66,67,68,69],"prolonged mechanical ventilation","ventilator weaning","lower limb muscle strengthening","exoskeleton robot","exercise training",{"date":33,"type":36},{"date":72,"type":36},"2026-06-26",{"date":74,"type":21},"2026-12-31",{"name":42,"class":43},{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":81,"acronym":4,"eligibilityCriteria":82,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":83,"targetDuration":4,"studyType":85,"phases":4,"briefSummary":86,"conditions":87,"keywords":92,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":101,"leadSponsor":102,"locationsCount":44},"100640569","regional-innovation-in-chronic-disease-and-elderly-care-100640569","NCT07578090","Regional Innovation in Chronic Disease and Elderly Care","A Regional Integrated Care Innovation Program for Cardiometabolic Health, Pulmonary-Circulatory Disease Management, and Elderly Support","Inclusion Criteria:\n\n* Participants with hypertension, hyperglycemia, or hyperlipidemia who meet at least one of these criteria are eligible for enrollment.\n\nExclusion Criteria:\n\n* Age under 18 years\n* Patients diagnosed with neuromuscular disorders\n* Inability to perform cardiopulmonary exercise testing\n* Refusal to participate in the study",{"count":84,"type":21},1000,"OBSERVATIONAL","This project aims to develop a community-based health promotion intervention model for populations at potential risk of metabolic syndrome. Through exercise training and lifestyle modifications, the project seeks to improve cardiopulmonary function and disease control, align with current public health policies, and establish an evidence-based model with strong potential for broader implementation.",[88,89,90,91],"Hypertension","Cardiovascular Disease","Hyperlipidemia","Hyperglycemia",[93,69,94,95,96],"hypertension","cardiovascular disease","hyperlipidemia","hyperglycemia","2026-05-26",{"date":99,"type":36},"2026-05-28",{"date":97,"type":36},{"date":74,"type":21},{"name":42,"class":43},{"id":104,"slug":105,"hasResults":11,"nctId":106,"briefTitle":107,"officialTitle":108,"acronym":4,"eligibilityCriteria":109,"healthyVolunteers":11,"sex":16,"minAge":110,"maxAge":18,"enrollmentInfo":111,"targetDuration":4,"studyType":22,"phases":112,"briefSummary":113,"conditions":114,"keywords":116,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":122,"lastUpdatePostDateStruct":123,"startDateStruct":125,"completionDateStruct":127,"leadSponsor":128,"locationsCount":44},"100631227","nutritional-effects-in-cardiovascular-surgery-100631227","NCT07497932","Nutritional Effects in Cardiovascular Surgery","Nutritional Intervention in the Modulation of Postoperative Metabolism in Cardiovascular Surgery","Inclusion Criteria:\n\n* Scheduled to undergo cardiovascular surgery\n* Completed preoperative clinical and imaging evaluations\n* Willing to provide informed consent\n* Willing to receive potential probiotic supplementation\n\nExclusion Criteria:\n\n* Use of antibiotics, probiotics, or other treatments affecting gut microbiota within 4 weeks\n* History of major gastrointestinal disease","50 Years",{"count":55,"type":21},[24],"This study aims to investigate the distribution of gut microbiota-derived metabolites, and to evaluate whether postoperative nutritional intervention can modulate the gut-heart metabolic axis, thereby improving metabolic profiles and clinical outcomes.",[115,89],"Cardiovascular Surgery",[117,118,119,120,121],"Gut microbiota-derived metabolites","Metabolomics","Cardiovascular disease","Nutritional intervention","Mass spectrometry","2026-03-23",{"date":124,"type":36},"2026-03-27",{"date":126,"type":36},"2026-03-19",{"date":74,"type":21},{"name":42,"class":43},{"id":130,"slug":131,"hasResults":11,"nctId":132,"briefTitle":133,"officialTitle":134,"acronym":4,"eligibilityCriteria":135,"healthyVolunteers":136,"sex":16,"minAge":137,"maxAge":138,"enrollmentInfo":139,"targetDuration":4,"studyType":85,"phases":4,"briefSummary":141,"conditions":142,"keywords":145,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":150,"lastUpdatePostDateStruct":151,"startDateStruct":153,"completionDateStruct":155,"leadSponsor":156,"locationsCount":44},"100630063","dementia-in-fiction-and-clinical-narratives-100630063","NCT07482800","Dementia in Fiction and Clinical Narratives","Examining Representations of Dementia in Fiction and Clinical Narratives","Inclusion Criteria:\n\n* Diagnosed with early-stage Alzheimer's disease or other mild cognitive impairment by a neurologist (case group) \u002F healthy individuals matched for age and education level (control group)\n* Able to communicate and understand basic language\n\nExclusion Criteria:\n\n* Refuse to participate in the study",true,"60 Years","85 Years",{"count":140,"type":21},40,"This study aims to compare the natural narrative language of patients with Alzheimer's disease and the fictional depictions of dementia in contemporary novels from both neurological and literary perspectives. It investigates the similarities and differences in the deterioration of semantic and episodic memory. The goal is to develop a cross-disciplinary language observation model that enhances early diagnostic understanding, fosters empathy in caregiving, and strengthens medical humanities education.",[143,144],"Dementia","Alzheimer s Disease",[143,146,147,148,149],"Language Decline","Neurology","Narrative Medicine","Literary Analysis","2026-03-18",{"date":152,"type":36},"2026-03-20",{"date":154,"type":36},"2026-03-17",{"date":40,"type":21},{"name":42,"class":43},{"id":158,"slug":159,"hasResults":11,"nctId":160,"briefTitle":161,"officialTitle":162,"acronym":4,"eligibilityCriteria":163,"healthyVolunteers":136,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":164,"targetDuration":4,"studyType":85,"phases":4,"briefSummary":166,"conditions":167,"keywords":169,"overallStatus":175,"whyStopped":4,"lastUpdateSubmitDate":176,"lastUpdatePostDateStruct":177,"startDateStruct":178,"completionDateStruct":180,"leadSponsor":181,"locationsCount":182},"100629403","expression-of-slc25a48-in-chronic-obstructive-pulmonary-disease-100629403","NCT07474220","Expression of SLC25A48 in Chronic Obstructive Pulmonary Disease","Association Between SLC25A48 Expression and Chronic Obstructive Pulmonary Disease Progression","Inclusion Criteria:\n\n* pre-COPD or COPD stages I-IV as per the 2023 GOLD guidelines (case group)\n* healthy individuals without chronic diseases or major medical conditions\n\nExclusion Criteria:\n\n* diagnosed with neuromuscular diseases\n* experienced respiratory disease exacerbation requiring emergency care or hospitalization in the past three months\n* assessed by a physician to have severe malnutrition or a significantly low BMI\n* continuously taking folic acid supplements\n* willing to receive or have already received self-paid nutrition clinic services at this hospital",{"count":165,"type":21},180,"This study aims to investigate the expression level of SLC25A48, a mitochondrial choline transporter, in peripheral blood mononuclear cells of patients with chronic obstructive pulmonary disease, and to analyze its correlation with inflammatory markers and choline metabolic byproducts.",[168],"Chronic Obstructive Pulmonary Disease",[170,171,172,173,174],"Chronic obstructive pulmonary disease","Mitochondrial choline transport","SLC25A48","Inflammatory markers","Choline metabolism","NOT_YET_RECRUITING","2026-03-14",{"date":154,"type":36},{"date":179,"type":21},"2026-04-01",{"date":74,"type":21},{"name":42,"class":43},2,{"id":184,"slug":185,"hasResults":11,"nctId":186,"briefTitle":187,"officialTitle":188,"acronym":4,"eligibilityCriteria":189,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":190,"targetDuration":4,"studyType":85,"phases":4,"briefSummary":191,"conditions":192,"keywords":196,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":201,"lastUpdatePostDateStruct":202,"startDateStruct":204,"completionDateStruct":206,"leadSponsor":207,"locationsCount":44},"100593924","pleural-effusion-biomarkers-in-lung-adenocarcinoma-patients-100593924","NCT07012759","Pleural Effusion Biomarkers in Lung Adenocarcinoma Patients","Novel Pleural Effusion Biomarkers Screening and Evaluation in Lung Adenocarcinoma Patients","Inclusion Criteria:\n\n* Patients requiring thoracentesis for pleural effusion drainage as determined by a physician based on clinical need.\n* Signed informed consent.\n\nExclusion Criteria:\n\n* Patients under the age of 18.\n* Patients with malignancies other than lung adenocarcinoma.",{"count":20,"type":21},"This project aims to assess the expression levels of novel molecular markers identified through screening in clinical samples of malignant pleural effusion, to evaluate the feasibility and clinical utility of these markers as potential diagnostic genes for lung adenocarcinoma.",[193,194,195],"Biomarkers","Lung Adenocarcinoma","Pleural Effusion",[197,198,199,200],"Pleural effusion","biomarkers","lung cancer","clinical diagnosis","2026-03-04",{"date":203,"type":36},"2026-03-05",{"date":205,"type":36},"2025-06-10",{"date":74,"type":21},{"name":42,"class":43},{"id":209,"slug":210,"hasResults":11,"nctId":211,"briefTitle":212,"officialTitle":213,"acronym":4,"eligibilityCriteria":214,"healthyVolunteers":11,"sex":16,"minAge":215,"maxAge":216,"enrollmentInfo":217,"targetDuration":4,"studyType":85,"phases":4,"briefSummary":219,"conditions":220,"keywords":223,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":229,"lastUpdatePostDateStruct":230,"startDateStruct":231,"completionDateStruct":233,"leadSponsor":234,"locationsCount":44},"100627389","multimodal-deep-learning-model-for-predicting-the-apnea-hypopnea-index-in-obstructive-sleep-100627389","NCT07447999","Multimodal Deep Learning Model for Predicting the Apnea-Hypopnea Index in Obstructive Sleep","A Multisensor Deep Neural Framework Combining Digital Auscultation, Oxygen Saturation, and Motion Data to Estimate the Apnea-Hypopnea Index in Obstructive Sleep Apnea","Inclusion Criteria:\n\n* age 30-75 years\n* clinically suspected obstructive sleep apnea and scheduled for polysomnography\n* willing and able to provide written informed consent\n\nExclusion Criteria:\n\n* intolerance to the electronic stethoscope or fingertip pulse oximeter\n* significant structural airway abnormalities\n* arrhythmia\n* neuromuscular disorders\n* pregnancy\n* hospitalization within the past 1 month\n* inability to provide informed consent or requiring legal guardian consent","30 Years","75 Years",{"count":218,"type":21},150,"This study aims to develop a multimodal deep learning model that integrates noninvasive signals to predict the severity of obstructive sleep apnea. By establishing a clinically viable and user-friendly monitoring tool, the study seeks to enhance early screening accessibility and support the development of home-based sleep care systems.",[221,222],"Obstructive Sleep Apnea (OSA)","Polysomnography",[224,225,226,227,228],"obstructive sleep apnea","polysomnography","ballistocardiography","electronic stethoscope","oxygen saturation","2026-03-03",{"date":203,"type":36},{"date":232,"type":36},"2025-09-05",{"date":40,"type":21},{"name":42,"class":43},{"id":236,"slug":237,"hasResults":11,"nctId":238,"briefTitle":239,"officialTitle":240,"acronym":4,"eligibilityCriteria":241,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":242,"targetDuration":4,"studyType":22,"phases":244,"briefSummary":245,"conditions":246,"keywords":250,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":256,"lastUpdatePostDateStruct":257,"startDateStruct":259,"completionDateStruct":261,"leadSponsor":262,"locationsCount":44},"100571239","probiotics-in-pulmonaty-rehabilitation-for-copd-100571239","NCT06717659","Probiotics in Pulmonaty Rehabilitation for COPD","Probiotics in the Management of Pulmonary Rehabilitation for COPD: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Willing to sign a written informed consent form.\n* Diagnosed with pre-COPD or COPD stage I-IV according to the 2023 GOLD guidelines.\n* Undergoing pulmonary rehabilitation therapy for more than three months.\n\nExclusion Criteria:\n\n* Under 18 years old.\n* Diagnosed with neuromuscular diseases.\n* Experienced respiratory disease exacerbation requiring emergency care or hospitalization in the past three months.\n* Unable to cooperate with cardiopulmonary exercise testing.\n* Has other diseases or behavioral restrictions preventing participation in exercise training for over one year.\n* Assessed by a physician to have severe malnutrition or a significantly low BMI.",{"count":243,"type":21},60,[24],"This study aims to investigate various aspects of patients with chronic respiratory diseases undergoing pulmonary rehabilitation supplemented with probiotics. The focus will be on clinical physiological responses, functional performance, respiratory status assessments, nutritional status evaluations, body composition analyses, and biochemical blood parameters, with a primary emphasis on the anti-inflammatory response.",[247,248,249],"COPD (Chronic Obstructive Pulmonary Disease)","Probiotic Intervention","Body Composition Measurement",[251,252,253,254,255],"body composition","inflammation markers","nutritional supplementation","probiotics","chronic obstructive pulmonary disease","2026-02-25",{"date":258,"type":36},"2026-02-27",{"date":260,"type":36},"2024-12-05",{"date":74,"type":21},{"name":42,"class":43},{"id":264,"slug":265,"hasResults":11,"nctId":266,"briefTitle":267,"officialTitle":268,"acronym":4,"eligibilityCriteria":269,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":270,"enrollmentInfo":271,"targetDuration":4,"studyType":85,"phases":4,"briefSummary":272,"conditions":273,"keywords":275,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":256,"lastUpdatePostDateStruct":280,"startDateStruct":281,"completionDateStruct":283,"leadSponsor":285,"locationsCount":44},"100560592","pressure-sensing-mattresses-and-mechanical-ventilation-weaning-in-neonatal-100560592","NCT06579157","Pressure-Sensing Mattresses and Mechanical Ventilation Weaning in Neonatal","The Association Between Pressure-Sensing Mattresses and Mechanical Ventilation Weaning in Neonatal","Inclusion Criteria:\n\n* Using invasive ventilation support with flow sensors or non-invasive ventilation support\n* The legal representative signs the informed consent form\n\nExclusion Criteria:\n\n* Refusal to participate in the study","1 Year",{"count":243,"type":21},"This study aims to explore the correlation between using ballistocardiography for monitoring respiration and heart rate in neonates under invasive and non-invasive respiratory support.",[274],"Bronchopulmonary Dysplasia",[276,277,278,279],"newborn","ballistocardiograph","pressure sensor","unobtrusive sensing",{"date":258,"type":36},{"date":282,"type":36},"2024-11-10",{"date":284,"type":21},"2027-07-31",{"name":42,"class":43},{"id":287,"slug":288,"hasResults":11,"nctId":289,"briefTitle":290,"officialTitle":291,"acronym":4,"eligibilityCriteria":292,"healthyVolunteers":136,"sex":16,"minAge":52,"maxAge":53,"enrollmentInfo":293,"targetDuration":4,"studyType":85,"phases":4,"briefSummary":294,"conditions":295,"keywords":296,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":256,"lastUpdatePostDateStruct":300,"startDateStruct":301,"completionDateStruct":303,"leadSponsor":304,"locationsCount":44},"100560647","association-between-cardiopulmonary-function-and-plantar-pressure-in-patients-with-chronic-obstructive-pulmonary-disease-100560647","NCT06579872","Association Between Cardiopulmonary Function and Plantar Pressure in Patients With Chronic Obstructive Pulmonary Disease","Association Between Cardiopulmonary Function, Mobility, Walking Ability, and Plantar Pressure Changes in Patients With Chronic Obstructive Pulmonary Disease: A Case-Control Study","Inclusion Criteria:\n\n* Age between 45 and 65 years\n* Patients with chronic respiratory diseases requiring pulmonary rehabilitation\n* Signed informed consent form\n\nExclusion Criteria:\n\n* Current tracheostomy\n* Home use of oxygen therapy or ventilators\n* Diagnosed with severe left heart failure (NYHA III-IV)\n* Patients diagnosed with neuromuscular diseases\n* Had an acute exacerbation of COPD in the past three months\n* Unable to perform cardiopulmonary exercise testing",{"count":243,"type":21},"It aims to understand the differences in everyday mobility and activity capabilities among patients with varying disease progression and severity, to serve as reference indicators for evaluating the effectiveness of pulmonary rehabilitation exercise training.",[168],[255,297,298,299],"plantar pressure","pulmonary rehabilitation","6-minute walk test",{"date":258,"type":36},{"date":302,"type":36},"2024-12-12",{"date":74,"type":21},{"name":42,"class":43},{"id":306,"slug":307,"hasResults":11,"nctId":308,"briefTitle":309,"officialTitle":310,"acronym":4,"eligibilityCriteria":311,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":312,"enrollmentInfo":313,"targetDuration":4,"studyType":22,"phases":314,"briefSummary":315,"conditions":316,"keywords":318,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":256,"lastUpdatePostDateStruct":324,"startDateStruct":325,"completionDateStruct":327,"leadSponsor":328,"locationsCount":44},"100533807","effect-of-diluent-volume-on-colistin-inhalation-therapy-100533807","NCT06230614","Effect of Diluent Volume on Colistin Inhalation Therapy","Effect of Diluent Volume on Colistin Inhalation Therapy for Mechanically Ventilated Respiratory Patients","Inclusion Criteria:\n\n* Admitted to the Intensive Care Unit.\n* Age greater than 18 years and using a ventilator due to acute respiratory failure.\n* Requires inhalation colistin treatment as determined by the disease.\n* Sign the written informed consent form.\n\nExclusion Criteria:\n\n* Renal failure requiring renal dialysis.\n* Receiving both inhaled colistin and intravenous colistin treatments.","100 Years",{"count":243,"type":21},[24],"The aim of this study is to investigate the impact of different diluent volumes for the same dosage of colistin in mechanically ventilated respiratory patients receiving colistin inhalation therapy. The study aims to determine whether the diluent volume has an effect on clinical outcomes, including ICU length of stay, total hospitalization duration, duration of respiratory support within 28 days, mortality rates within 28 days and 90 days, as well as analyze the pharmacokinetic profile of colistin in blood and bronchoalveolar lavage fluid. Additionally, the study will evaluate the incidence of nebulizer malfunctions and blockages. The findings of this research will help identify the optimal diluent volume for colistin inhalation therapy in clinical practice.",[317],"Inhalation Pneumonia",[319,320,321,322,323],"Colistin","antibiotic","inhalation therapy","diluent volume","randomized controlled trial",{"date":258,"type":36},{"date":326,"type":36},"2024-03-10",{"date":40,"type":21},{"name":42,"class":43},{"id":330,"slug":331,"hasResults":11,"nctId":332,"briefTitle":333,"officialTitle":334,"acronym":4,"eligibilityCriteria":335,"healthyVolunteers":136,"sex":16,"minAge":17,"maxAge":215,"enrollmentInfo":336,"targetDuration":4,"studyType":22,"phases":338,"briefSummary":339,"conditions":340,"keywords":342,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":256,"lastUpdatePostDateStruct":347,"startDateStruct":348,"completionDateStruct":350,"leadSponsor":352,"locationsCount":44},"100529227","use-of-3d-printing-high-fidelity-craniofacial-manikin-to-teach-noninvasive-positive-pressure-ventilation-100529227","NCT06171035","Use of 3D Printing High-fidelity Craniofacial Manikin to Teach Noninvasive Positive Pressure Ventilation","Use of 3D Printing High-fidelity Airway and Craniofacial Manikin as an Education Tool to Improve Learning Efficiency of Teaching Noninvasive Positive Pressure Ventilation","Inclusion Criteria:\n\n* Student of Fu Jen Catholic University\n\nExclusion Criteria:\n\n* Refused to participate in the study",{"count":337,"type":21},50,[24],"The aim of this study is to enhance the learning efficiency and ability of problem-solving for student of Department of Respiratory Therapy with the innovative 3D printing high-fidelity manikin.",[341],"Satisfaction, Personal",[343,344,345,346],"3D printing","medical education model","high-fidelity simulation","respiratory care",{"date":258,"type":36},{"date":349,"type":36},"2023-12-07",{"date":351,"type":21},"2026-08-31",{"name":42,"class":43},{"id":354,"slug":355,"hasResults":11,"nctId":356,"briefTitle":357,"officialTitle":358,"acronym":4,"eligibilityCriteria":359,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":360,"targetDuration":4,"studyType":22,"phases":362,"briefSummary":363,"conditions":364,"keywords":366,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":256,"lastUpdatePostDateStruct":370,"startDateStruct":371,"completionDateStruct":373,"leadSponsor":374,"locationsCount":44},"100527381","utilizing-3d-printed-personalized-aortic-lesion-models-in-preoperative-assessment-100527381","NCT06147024","Utilizing 3D Printed Personalized Aortic Lesion Models in Preoperative Assessment","Utilizing 3D Printed Personalized Aortic Lesion Models to Assist Surgeons in Preoperative Assessment and Planning of Aortic Aneurysm Surgery","Inclusion Criteria:\n\n* Diagnosed with thoracic or abdominal aortic aneurysm\n* Signed surgical consent\n* Non-emergent surgery\n* Had 2D CT imaging within the last 6 months\n\nExclusion Criteria:\n\n* Refusal to use lesion images for model creation\n* Refusal to participate in the study",{"count":361,"type":21},10,[24],"Using 3D printing technology to create personalized models of diseased heart and aortic blood vessels, surgeons can perform preoperative planning and evaluate relevant indicators.",[365],"Aortic Aneurysm",[343,367,368,369],"pre-operative planning","thoracic aorta aneurysm","abdominal aorta aneurysm",{"date":258,"type":36},{"date":372,"type":36},"2024-04-08",{"date":284,"type":21},{"name":42,"class":43},{"id":376,"slug":377,"hasResults":11,"nctId":378,"briefTitle":379,"officialTitle":380,"acronym":4,"eligibilityCriteria":381,"healthyVolunteers":11,"sex":16,"minAge":382,"maxAge":18,"enrollmentInfo":383,"targetDuration":4,"studyType":22,"phases":385,"briefSummary":386,"conditions":387,"keywords":389,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":395,"lastUpdatePostDateStruct":396,"startDateStruct":398,"completionDateStruct":400,"leadSponsor":402,"locationsCount":44},"100529014","effects-of-eccentric-exercise-training-in-patients-with-copd-100529014","NCT06168266","Effects of Eccentric Exercise Training in Patients With COPD","Effects of Smart Eccentric Exercise Training on Lymphocyte Immunity and Erythrocyte Rheology in Patients With Chronic Obstructive Pulmonary Disease","Inclusion Criteria:\n\n* Having undergone pulmonary rehabilitation for more than 3 months\n* Sign the written informed consent form\n* FEV1\u002FFVC \\\u003C 0.70\n* Approval for exercise training granted by a specialist physician's assessment\n* Specialist physician's approval for exercise training\n\nExclusion Criteria:\n\n* Existing of tracheostomy\n* Those who use oxygen therapy or ventilator at home\n* Severe heart failure (NYHA III-IV)\n* Neuromuscular disease\n* Acute exacerbation within the past three months\n* Those who are unable to cooperate with the cardiopulmonary exercise test\n* Taking anticoagulant medications\n* Other conditions restricting exercise for over a year\n* Recent or planned significant cardiovascular surgery or intervention\n* Current or planned pregnancy within the next year\n* Planned heart transplant within the next six months\n* Heart failure due to uncorrectable valvular heart disease, congenital heart disease or obstructive cardiomyopathy\n* Inadequate ICD settings for exercise heart rate\n* Other exercise contraindications: unstable angina, uncontrolled blood pressure, orthostatic hypotension with symptoms, severe aortic stenosis, acute discomfort or fever, uncontrolled arrhythmias, uncompensated heart failure, acute pericarditis or myocarditis, recent thrombosis or thrombophlebitis, resting ST-segment deviation, uncontrolled diabetes, etc.","20 Years",{"count":384,"type":21},170,[24],"The goal of this study is to design eccentric exercise strategies for COPD patients to comprehensively improve their cardiopulmonary\u002Fmuscular fitness, immune and hemorheological functions, and quality of life, thereby improving the prognosis of their disease.",[388],"COPD",[388,390,391,392,393,394],"Eccentric Exercise Training","Lymphocytes","Mitochondria","Erythrocytes","Rheology","2026-02-10",{"date":397,"type":36},"2026-02-12",{"date":399,"type":36},"2023-12-13",{"date":401,"type":21},"2027-12-30",{"name":42,"class":43},{"id":404,"slug":405,"hasResults":11,"nctId":406,"briefTitle":407,"officialTitle":408,"acronym":4,"eligibilityCriteria":409,"healthyVolunteers":136,"sex":16,"minAge":17,"maxAge":215,"enrollmentInfo":410,"targetDuration":4,"studyType":22,"phases":411,"briefSummary":412,"conditions":413,"keywords":416,"overallStatus":175,"whyStopped":4,"lastUpdateSubmitDate":419,"lastUpdatePostDateStruct":420,"startDateStruct":422,"completionDateStruct":424,"leadSponsor":425,"locationsCount":4},"100567576","comparison-of-teaching-effectiveness-of-vr-video-and-written-materials-on-food-hygiene-and-equipment-safety-100567576","NCT06669988","Comparison of Teaching Effectiveness of VR, Video, and Written Materials on Food Hygiene and Equipment Safety","Comparison of the Teaching Effectiveness of VR, Videos, and Written Materials on Food Hygiene Safety and Equipment Operation","Inclusion Criteria:\n\n* native Chinese speakers\n* normal vision, hearing, and hand mobility\n\nExclusion Criteria:\n\n* in other VR-related studies\n* symptoms of dizziness when wearing a virtual reality headset\n* have taken courses in food service or food hygiene and safety",{"count":243,"type":21},[24],"This study investigates the impact of virtual reality (VR) as an educational tool in the food industry, comparing it to traditional methods like videos and written materials in teaching hygiene and safety. VR offers immersive, realistic training that allows employees to simulate food-handling scenarios, including handwashing, hazard identification, and emergency responses, which may enhance engagement and effectiveness. The study aims to clarify the advantages and limitations of VR-based education against traditional approaches by assessing learning effectiveness, usefulness, playfulness, ease of use, and long-term knowledge retention.\n\nParticipants will be assigned to one of the three educational methods (VR, video, or written materials) and evaluated through pre-tests, post-tests, and follow-up assessments one month later. Non-parametric statistical analysis, specifically the Wilcoxon signed-rank test, will assess the effectiveness of each educational method based on test scores and satisfaction surveys.\n\nThe study will be conducted at Fu Jen Catholic University's Department of Nutrition, following ethical guidelines and informed consent protocols to protect participants' welfare and data privacy. Professional supervision and carefully maintained equipment will ensure a safe learning environment, with adverse reactions monitored and documented throughout.",[414,415],"Educational Interventions","Virtual Reality",[415,417,418],"education","hygiene safety in food service","2024-10-31",{"date":421,"type":36},"2024-11-01",{"date":423,"type":21},"2025-02-01",{"date":351,"type":21},{"name":42,"class":43},{"id":427,"slug":428,"hasResults":11,"nctId":429,"briefTitle":430,"officialTitle":431,"acronym":4,"eligibilityCriteria":432,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":433,"targetDuration":4,"studyType":22,"phases":435,"briefSummary":436,"conditions":437,"keywords":440,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":444,"lastUpdatePostDateStruct":445,"startDateStruct":447,"completionDateStruct":449,"leadSponsor":451,"locationsCount":44},"100548153","effects-of-a-3d-printed-port-a-catheter-model-training-course-100548153","NCT06417294","Effects of a 3D-Printed Port-A Catheter Model Training Course","Effects of a 3D-Printed Port-A Catheter Model Training Course for Patient Discharge Instruction","Inclusion Criteria:\n\n* Admitted to the hematology and oncology ward of Fu Jen Catholic University Hospital\n* Have Chinese communication skills\n\nExclusion Criteria:\n\n* Refused to participate in the study.",{"count":434,"type":21},120,[24],"The aim of this study is to develop a highly realistic 3D-printed Port-A catheter upper body model to improve the knowledge and self-care skills of patients and primary caregivers regarding Port-A catheter placement through patient education.",[438,439],"Patient Satisfaction","Cancer",[441,442,443],"3D printed model","port-a catheter","discharge education","2024-06-07",{"date":446,"type":36},"2024-06-10",{"date":448,"type":36},"2024-06-01",{"date":450,"type":21},"2024-12-31",{"name":42,"class":43},""]