[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"pediatric-emergency-medicine\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:pediatric-emergency-medicine":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,46,79,108,131],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":32,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100521862","the-p-kids-care-health-systems-intervention-in-tanzania-100521862",false,"NCT06075108","The P-KIDs CARE Health Systems Intervention in Tanzania","P-KIDs CARE: An Intervention to Address Health Systems Delays to Care for Injured Children in Tanzania","P-KIDs CARE","Inclusion Criteria:\n\n* AIM 1 (mixed methods research)\n\n  1. Enroll into the pediatric injury registry all pediatric (\\\u003C18 years old) patients seeking care at one of the study health facilities for an acute injury.\n  2. The investigators will conduct in-depth interviews with the following group: Family members of a pediatric injury patients seeking care at the study facilities.\n  3. The investigators will conduct focus group discussions with the following group: Health care providers providing care to pediatric injury patients at the study facilities.\n* AIM 2 (develop intervention)\n\n  1. The investigators will hold a 2-day intervention development workshop with the interdisciplinary study team.\n  2. The investigators will conduct focus group discussions with the following groups:\n\n     1. Health care providers providing care to pediatric injury patients at the study health facilities\n     2. A community-engaged panel including family members of pediatric injury patients\n* AIM 3 (pilot intervention)\n\n  1. The investigators will enroll into the pediatric injury registry all pediatric (\\\u003C18 years old) patients seeking care at one of the study health facilities for an acute injury.\n  2. The investigators will conduct surveys and exit interviews with the following groups:\n\n     1. Health care providers providing care to pediatric injury patients at the study health facilities.\n     2. Family members of pediatric injury patients.","ALL",{"count":19,"type":20},284,"ESTIMATED","INTERVENTIONAL",[23],"NA","The objective of the proposed research is to develop and pilot a locally-relevant, multicomponent intervention to streamline the triage process (e.g. patient assessment, stabilization, and disposition) for pediatric injury patients in Tanzania. This health systems intervention will work at the first level of medical contact (e.g., health center and district hospital), in order to facilitate timely disposition and referrals, and subsequently decrease time to definitive care. The proposed study has three aims: 1) With a mixed methods approach, describe the barriers to pediatric injury care at the first medical contact; 2) Iteratively develop the P-KIDs CARE intervention using a nominal group technique and conduct a pre-implementation assessment and refinement; 3) Pilot the P-KIDs CARE intervention and perform an implementation-focused formative evaluation. The proposed study focuses on pediatric injury patients and the family members and healthcare providers that care for them in Kilimanjaro, Tanzania. The investigators will recruit pediatric injury patients, family members, and healthcare providers from 2 health facilities in the Kilimanjaro Region.",[26,27,28,29,30,31],"Accidental Injuries","Global Child Health","Pediatric Emergency Medicine","Public Health System Research","Health Care Providers","Implementation Science",[26,27,28,30,29,31],"RECRUITING","2026-01-14",{"date":36,"type":37},"2026-01-16","ACTUAL",{"date":39,"type":37},"2024-08-05",{"date":41,"type":20},"2028-08-31",{"name":43,"class":44},"University of Utah","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":53,"sex":17,"minAge":54,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":21,"phases":57,"briefSummary":58,"conditions":59,"keywords":61,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":78},"100482077","effectiveness-of-a-mobile-app-in-reducing-therapeutic-tat-in-an-emergency-department-100482077","NCT05557331","Effectiveness of a Mobile App in Reducing Therapeutic TAT in an Emergency Department","Effectiveness of a Mobile App (PIMPmyHospital) in Reducing Therapeutic Turnaround Times in an Emergency Department: Protocol for a Pre-Post Intervention Study","Inclusion Criteria:\n\n* Any postgraduate residents pursuing a \\\u003C6 years residency in pediatrics.\n* Any pediatric emergency medicine fellows.\n* To be registered nurses from the pediatric emergency department.\n* Participation agreement.\n\nExclusion Criteria:\n\n* none",true,"18 Years",{"count":56,"type":20},18,[23],"This study is a single center, non-equivalent comparison group, pre-post study in a tertiary pediatric emergency department in Switzerland. the study will compare the control and experimental groups on outcome measures before (12-month period) and after (6-month period) the intervention consisting of the implementation and use of the evidence-based mobile app-the ''Patients In My Pocket in my Hospital'' (PIMPmyHospital) app.\n\nThe primary outcome will be the mean elapsed time in minutes between the delivery of lab results and the emergency department caregivers accessing them before (i.e., on the institutional electronic medical records) and after the implementation of the app (i.e, directly on the app).",[28,60],"Therapeutic Turnaround Time",[62,63,64,65,66,67,28,68],"Information technologies","Mobile Applications","Laboratory Result Delivery","Therapeutic turnaround time","Information Storage and Retrieval","Hospital Communication Systems","Emergency Department","2025-08-17",{"date":71,"type":37},"2025-08-19",{"date":73,"type":37},"2025-03-01",{"date":75,"type":20},"2025-12-01",{"name":77,"class":44},"Pediatric Clinical Research Platform",2,{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":4,"eligibilityCriteria":85,"healthyVolunteers":53,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":86,"targetDuration":4,"studyType":21,"phases":88,"briefSummary":89,"conditions":90,"keywords":95,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":99,"lastUpdatePostDateStruct":100,"startDateStruct":102,"completionDateStruct":104,"leadSponsor":106,"locationsCount":45},"100589624","immersive-virtual-reality-simulation-effects-of-self-guided-versus-facilitator-guided-debriefing-100589624","NCT06956833","Immersive Virtual Reality Simulation-Effects of Self-Guided Versus Facilitator-Guided Debriefing","Self-Guided Versus Facilitator-Guided Debriefing in Immersive Virtual Reality Simulation: Protocol for a Randomized Controlled Non-Inferiority Trial As-sessing Teamwork Skills in Medical Students","Inclusion Criteria:\n\n* Eligible participants will be medical students enrolled at medical schools in Denmark who are within two years of graduation.\n\nExclusion Criteria:\n\n* Lack of informed consent",{"count":87,"type":20},88,[23],"The goal of this clinical trial is to find out whether self-guided and facilitator-guided virtual reality (VR) simulations are equally effective in helping medical students learn how to manage and treat critically ill children. The study will also investigate how medical students feel about the two training methods and examine how many experience cybersickness. The main questions it aims to answer are:\n\n* Does self-guided VR simulation work as well as facilitator-guided VR simulation in teaching medical students how to manage critically ill children?\n* How do medical students experience the ease of use, workload, reflection on learning, and motivation in each training method?\n* How many students experience cybersickness? To answer these questions, researchers will compare the two training methods to evaluate if self-guided VR simulation is an effective way to teach medical students how to manage critically ill children.\n\nParticipants will:\n\n* Work through three VR cases to practice managing critically ill children in a safe environment.\n* Be tested before and after the VR simulation to assess changes in their skills managing critically ill children.\n* Complete surveys about their experience of the VR simulation, the training sessions, and any cybersickness symptoms they might have.",[91,92,28,93,94],"Virtual Reality Simulation","Simulation-based Medical Education","Immersive Virtual Reality","Debriefing",[93,96,97,98,94],"Virtual Reality simulation","Simulation-based medical education","Pediatric emergencies","2025-05-13",{"date":101,"type":37},"2025-05-14",{"date":103,"type":37},"2025-05-06",{"date":105,"type":20},"2025-10",{"name":107,"class":44},"Rigshospitalet, Denmark",{"id":109,"slug":110,"hasResults":11,"nctId":111,"briefTitle":112,"officialTitle":113,"acronym":4,"eligibilityCriteria":114,"healthyVolunteers":11,"sex":17,"minAge":115,"maxAge":54,"enrollmentInfo":116,"targetDuration":4,"studyType":118,"phases":4,"briefSummary":119,"conditions":120,"keywords":4,"overallStatus":121,"whyStopped":4,"lastUpdateSubmitDate":122,"lastUpdatePostDateStruct":123,"startDateStruct":125,"completionDateStruct":127,"leadSponsor":129,"locationsCount":4},"100560443","pattern-and-outcome-of-children-admitted-in-emergency-unit-of-assuit-children-university-hospital-hospital-100560443","NCT06577207","Pattern and Outcome of Children Admitted in Emergency Unit of Assuit Children University Hospital Hospital","Pattern and Outcome of Children Admitted in Emergency Unit of Assuit Children University Hospital","Inclusion Criteria:\n\n* All patients from 28 day till 18 years who will be admitted to emergency unite at (AUCH) during duration of the study,data of the patients will be collected in the form of :\n\n  * Full history taking:\n\n    1. Personal history: (age, sex, gestational age), residence and socioeconomic status.\n    2. Cause of admission and clinical characteristic of patients (medical or surgical condition).\n    3. Triage and acuity : rapidly screening of sick children in order to identify: • those with emergency signs, who require immediate emergency treatment; • those with priority signs, who are at higher risk of dying.\n\n       These children should be assessed without unnecessary delay. • non-urgent cases, who have neither emergency nor priority signs. Emergency signs include: obstructed or absent breathing, severe respiratory distress, central cyanosis, signs of shock, coma, convulsions, signs of severe dehydration . The priority signs include: any sick child aged \\\u003C 2 months, very high temperature, severe pallor, history of poisoning, severe pain, restless or continuously irritable, edema of both feet\n    4. Associated symptoms of different systems involved.\n    5. Provisional diagnosis.\n    6. 1 st admission or not\n    7. Referring center , time and seasonal variation to detect most peak area and months\n    8. Fate\n  * Complete physical examination: Including body temperature , respiratory rate, heart rate, pallor, weight loss, and evidence of dehydration. Chest, cardiac , abdominal and neurological examination.\n  * Investigations and Imaging: Initial investigations for all cases: 1. Pulse oximetry. 2. Complete blood count. 3. Electrolytes. 4. Kidney function test. 5. Random blood glucose 6. Other investigations ordered for certain cases according to clinical manifestation \\& previous findings \\> Lines of treatment will be recorded\n  * Patients will be followed during their stay in ER and till discharge patient to home or refer him to specific unit in pediatric hospital with monitoring of factors affecting their prognosis.\n\nExclusion Criteria:\n\n1. Neonates\n2. patients which their age are more than 18 years\n3. Patients which have recent trauma","28 Days",{"count":117,"type":20},93,"OBSERVATIONAL","In the present work, we aim to\n\n1. Describe the pattern of patients admitted to Emergency unite at Assiut University Child Hospital (AUCH) and classify them according to age ,distribution ,most common presenting complain, effect of seasonal variation on causes of admission ,prognosis till discharge of the patient to home or refer him to specific unit in pediatric hospital and associated chronic disease.\n2. Describe factors affecting mortality rate",[28],"NOT_YET_RECRUITING","2024-08-30",{"date":124,"type":37},"2024-09-03",{"date":126,"type":20},"2025-01",{"date":128,"type":20},"2027-01",{"name":130,"class":44},"Assiut University",{"id":132,"slug":133,"hasResults":11,"nctId":134,"briefTitle":135,"officialTitle":136,"acronym":4,"eligibilityCriteria":137,"healthyVolunteers":53,"sex":17,"minAge":138,"maxAge":4,"enrollmentInfo":139,"targetDuration":4,"studyType":21,"phases":141,"briefSummary":142,"conditions":143,"keywords":146,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":163,"lastUpdatePostDateStruct":164,"startDateStruct":166,"completionDateStruct":168,"leadSponsor":170,"locationsCount":78},"100499949","the-marvin-chatbots-to-provide-information-for-different-health-conditions-100499949","NCT05789901","The MARVIN Chatbots to Provide Information for Different Health Conditions","A Master Research Protocol to Adapt and Evaluate an Artificial Intelligence Based Conversational Agent to Provide Information for Different Health Conditions: the MARVIN Chatbots","Inclusion Criteria for all objectives:\n\n* being 14 years or older;\n* being fluent in English and\u002For French;\n* being able to understand the requirements of study participation and provide informed consent during the duration of the study;\n* having access to a smartphone, tablet, or computer at home\u002Fat workplace;\n* having access to an internet connection at home or data plan on their device.\n\nInclusion Criteria Specific to objectives 2 and 3:\n\n* accept to use a Facebook Messenger-based Chatbot;\n* accept to use or create a personal Facebook account;\n* accept Facebook's privacy and data security policies.\n\nExclusion Criteria:\n\n* not meeting the inclusion criteria\n* any reason, in the opinion of the investigator, which would make the candidate inappropriate for participation in an investigative study involving a chatbot (e.g., cognitive deficit)","14 Years",{"count":140,"type":20},400,[23],"This research is a continuation of a usability study with the MARVIN chatbot. The investigators aim to adapt the MARVIN chatbot to open it to other health domains (e.g. breast cancer) and populations (e.g. pharmacists). Therefore, this protocol constitutes a master research protocol that will englobe different research projects with individual chatbots. The investigators adopt an adaptive platform trial design, which will allow flexibility in handling multiple interventions adapted to different populations while retaining the characteristics of a platform trial design allowing early withdrawal of ineffective trial arms based on interim data (implementation outcomes) and introduction of new trial arms.",[144,145,28],"HIV Infections","Breast Cancer",[147,148,149,150,151,152,31,153,145,154,155,156,157,158,159,28,160,161,162],"Chatbot","Intelligent Conversational Agent","Co-Construction","Adherence","Antiretroviral Therapy","mHealth","Care","HIV","Self-Management","Adaptive Platform Trial Design","Telehealth","Digital Health","Artificial Intelligence","Patient and Stakeholder Engagement","Pediatric Infection","Large Language Models","2024-03-04",{"date":165,"type":37},"2024-03-06",{"date":167,"type":37},"2024-03-01",{"date":169,"type":20},"2034-12-31",{"name":171,"class":44},"McGill University Health Centre\u002FResearch Institute of the McGill University Health Centre"]