[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"health-personnel\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:health-personnel":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,51,73],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":33,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":46,"leadSponsor":48,"locationsCount":4},"100601547","virtual-reality-infection-control-training-for-healthcare-workers-during-the-hajj-season-100601547",false,"NCT07111910","Virtual Reality Infection Control Training for Healthcare Workers During the Hajj Season","Virtual Reality Training for Infection Control Preparedness in Healthcare Practitioners During Hajj: A Randomized Controlled Trial on Skill Acquisition and Clinical Readiness","(VIRTIC-Hajj)","Inclusion Criteria:\n\n* Aged 20 and above\n* Assigned to work in Hajj healthcare settings\n* Licensed healthcare worker (nurse, physician, EMT, etc.)\n* Able to provide informed consent\n* Fluent in Arabic or English\n\nExclusion Criteria:\n\n* History of epilepsy or motion sickness triggered by VR\n* Severe visual or cognitive impairments",true,"ALL","20 Years",{"count":21,"type":22},200,"ESTIMATED","INTERVENTIONAL",[25],"NA","The goal of this clinical trial is to evaluate the effectiveness of immersive virtual reality (VR) training on improving infection control preparedness among healthcare workers during the Hajj pilgrimage in Saudi Arabia.\n\nThe main questions this study aims to answer are:\n\nDoes VR training improve healthcare workers' knowledge, confidence, and preparedness for infection control compared to traditional training?\n\nAre there differences in outcomes between the VR training and traditional lecture-based education?",[28,29,30,31,32],"Infection Control Training","Clinical Competence","Virtual Reality","Health Personnel","Mass Gathering Medicine",[34,35,36,37,38],"Virtual Reality Training","Infection Control","Hajj Pilgrimage","Healthcare Workers","Simulation Education","NOT_YET_RECRUITING","2026-05-03",{"date":42,"type":43},"2026-05-07","ACTUAL",{"date":45,"type":22},"2026-09-20",{"date":47,"type":22},"2027-09-01",{"name":49,"class":50},"University of Bisha","OTHER",{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":58,"phases":4,"briefSummary":59,"conditions":60,"keywords":4,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":72},"100597882","assessment-of-interprofessional-competencies-of-healthcare-professionals-before-and-after-healthcare-simulation-sessions-100597882","NCT07064265","Assessment of Interprofessional Competencies of Healthcare Professionals Before and After Healthcare Simulation Sessions","Inclusion Criteria:\n\n* Medical students (interns and externs)\n* Paramedical students (nursing students, nurse assistants, nurse managers)\n* Healthcare professionals from Gonesse Hospital\n\nExclusion Criteria:\n\n* Administrative staff\n* Participants who have already taken part in previous simulation sessions",{"count":21,"type":22},"OBSERVATIONAL","The aim of our study is to assess the interprofessional competencies of healthcare learners before and one month after interprofessional simulation sessions, and to demonstrate their impact on the work of healthcare professionals as part of their continuing education in a hospital setting.\n\nInitially, we will distribute a self-assessment questionnaire to all learners before the simulation sessions and again one month after the sessions.\n\nHospital-based healthcare professionals register for the simulation training through the continuing education department of Gonesse Hospital.\n\nPhysicians and medical students register through the training's designated physician.\n\nParamedical students register through the training's designated nurse manager.\n\nWe conduct two simulation training sessions per month on the topic of \"Adult Life-Threatening Emergencies: Cardiac Arrest.\"\n\nEach session is composed of an interprofessional group.\n\nBefore the start of the session, the questionnaire is distributed to all participants.\n\nLearners are asked to indicate only their profession and the date on the questionnaire.\n\nEach questionnaire is assigned a number in the order of collection to ensure anonymity.\n\nOne month later, we resend the same questionnaire by email to the participants.\n\nThis is a self-assessment questionnaire developed in Canada and scientifically validated, used to evaluate interprofessional collaboration competencies (Survey for the Achievement of Interprofessional Collaborative Competencies: SACCI).\n\nIn a second phase, we will compare the results of the self-assessment questionnaires completed before and one month after the simulation sessions, using statistical analysis via Excel spreadsheet.",[31,61,62],"Interprofessional Relations","CONTINUING MEDICAL EDUCATION","2025-07-10",{"date":65,"type":43},"2025-07-14",{"date":67,"type":22},"2025-08-15",{"date":69,"type":22},"2026-03-15",{"name":71,"class":50},"Centre Hospitalier de Gonesse",1,{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":77,"acronym":4,"eligibilityCriteria":78,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":79,"enrollmentInfo":80,"targetDuration":4,"studyType":58,"phases":4,"briefSummary":82,"conditions":83,"keywords":4,"overallStatus":84,"whyStopped":4,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":72},"100565413","respiratory-virome-diversity-and-baseline-immunity-in-healthy-individuals-in-shanghai-100565413","NCT06641856","Respiratory Virome Diversity and Baseline Immunity in Healthy Individuals in Shanghai","1\\. Young Healthy Volunteers\n\nInclusion Criteria:\n\n1. Age between 20-35 years (inclusive), Han ethnicity, regardless of gender. Body Mass Index (BMI) between 19-26 kg\u002Fm² (inclusive), with a minimum weight of 50 kg for males and 45 kg for females.\n2. The participant must be in good overall health, as determined by medical history, physical examination, vital signs, and results from a health checkup within the past year (normal or clinically insignificant findings).\n3. Female participants must be non-pregnant and non-lactating.\n4. Able to tolerate bronchoscopy and willing to provide nasal and pharyngeal swabs, as well as upper and lower respiratory secretions and peripheral blood samples.\n5. Fully informed of the study's purpose, methods, and potential discomforts, with written informed consent provided, and willing to complete the study questionnaire.\n6. Good compliance and willingness to follow the study protocol and complete follow-up procedures.\n\nExclusion Criteria:\n\n1. Non-permanent residents of Shanghai who have stayed in the city for more than 30 days; or permanent residents of Shanghai who have left the city within the past 30 days.\n2. History of significant illness or major surgery within the past 30 days, or anticipation of major surgery during the study period.\n3. Diagnosis of respiratory diseases (infectious or non-infectious) within the past 30 days, requiring medication (oral, inhaled, or nebulized).\n4. Presence of clinically significant diseases or factors, including but not limited to neurological, cardiovascular, hematologic, hepatic, renal, gastrointestinal, respiratory, metabolic, endocrine, immune, skeletal diseases, or other conditions deemed unsuitable by the investigator.\n5. Long-term use of medication.\n6. Positive test results for HIV antibodies (HIV-Ab), hepatitis B surface antigen (HBsAg), hepatitis C antibodies (HCV-Ab), or syphilis antibodies (TP-Ab).\n7. Participation in any drug or medical device clinical trial within the past 3 months.\n8. Vaccination within the past 30 days or planned vaccination during the study period.\n9. Any other condition deemed by the investigator to impact the participant's ability to provide informed consent, follow the protocol, or affect study outcomes or the participant's safety.\n\n2\\. Elderly Healthy Volunteers\n\nInclusion Criteria:\n\n1. Age between 60-75 years (inclusive), Han ethnicity, regardless of gender. Body Mass Index (BMI) between 19-26 kg\u002Fm² (inclusive), with a minimum weight of 50 kg for males and 45 kg for females.\n2. The participant must have a healthy respiratory system, as determined by medical history, physical examination, vital signs, and results from a health checkup within the past year (normal or clinically insignificant findings).\n3. Able to tolerate bronchoscopy and willing to provide nasal and pharyngeal swabs, as well as upper and lower respiratory secretions and peripheral blood samples.\n4. Fully informed of the study's purpose, methods, and potential discomforts, with written informed consent provided, and able to independently complete the study questionnaire.\n5. Good compliance and willingness to follow the study protocol and complete follow-up procedures.\n\nExclusion Criteria:\n\n1. Non-permanent residents of Shanghai who have stayed in the city for more than 30 days; or permanent residents of Shanghai who have left the city within the past 30 days.\n2. History of significant illness or major surgery within the past 30 days, or anticipation of major surgery during the study period.\n3. Diagnosis of respiratory diseases (infectious or non-infectious) within the past 30 days, requiring medication (oral, inhaled, or nebulized).\n4. Presence of abnormal respiratory system function or other clinically significant diseases or conditions.\n5. History of malignant tumors (including hematologic malignancies or solid tumors).\n6. Long-term use of medication.\n7. Positive test results for HIV antibodies (HIV-Ab), hepatitis B surface antigen (HBsAg), hepatitis C antibodies (HCV-Ab), or syphilis antibodies (TP-Ab).\n8. Participation in any drug or medical device clinical trial within the past 3 months.\n9. Vaccination within the past 30 days or planned vaccination during the study period.\n10. Any other condition deemed by the investigator to impact the participant's ability to provide informed consent, follow the protocol, or affect study outcomes or the participant's safety.","75 Years",{"count":81,"type":22},300,"This study investigates the diversity of the respiratory virome in healthy individuals in Shanghai and its interaction with the host's baseline immune response. The respiratory virome plays a critical role in various diseases, but research on the respiratory virome in healthy individuals in China is limited. This prospective study will analyze the upper and lower respiratory virome and examine the effects of demographic factors such as age, gender, and geographic background. Additionally, a respiratory virome database will be established, and multi-omics approaches will be used to study immune response mechanisms in relation to virome diversity.",[31],"RECRUITING","2024-10-25",{"date":87,"type":43},"2024-10-29",{"date":89,"type":43},"2024-09-02",{"date":91,"type":22},"2026-12-31",{"name":93,"class":50},"Ruijin Hospital"]