[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"physician-burnout\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:physician-burnout":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,57,86],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":34,"overallStatus":44,"whyStopped":4,"lastUpdateSubmitDate":45,"lastUpdatePostDateStruct":46,"startDateStruct":49,"completionDateStruct":51,"leadSponsor":53,"locationsCount":56},"100634675","choice-and-autonomy-in-learning-mindfulness-for-pediatric-residents-100634675",false,"NCT07542769","Choice and Autonomy in Learning Mindfulness for Pediatric Residents","CALM-PR","Inclusion Criteria:\n\n* Current categorical pediatrics residents at Northwestern University.\n* Preliminary pediatrics residents who intend to continue in pediatrics.\n* Willing and able to provide informed consent.\n\nExclusion Criteria:\n\n\\- None; all pediatric residents meeting inclusion criteria are eligible.",true,"ALL",{"count":19,"type":20},42,"ESTIMATED","INTERVENTIONAL",[23],"NA","This study is a pilot clinical trial designed to evaluate a flexible, online mindfulness program for pediatric residents. Medical training can be stressful, and although mindfulness programs are often offered to support well-being, many are either in-person or follow a fixed format that may not fit individual schedules or preferences. This study will test a digital mindfulness program called Wakeful, which allows participants to complete the course at their own pace. Participants will be randomly assigned to one of two groups: one group will be able to choose the length of their mindfulness program (3, 5, or 7 weeks), while the other group will be assigned a program length without a choice. The goal is to understand whether giving participants a choice improves how often they use the program, how satisfied they are with it, and whether they complete it. The main outcomes of this study focus on how participants interact with the program, including how many sessions they complete, how often they practice mindfulness on their own, and how useful and relevant they find the program. The study will also look at overall satisfaction and how many participants drop out before finishing. In addition, the study will explore whether participants report changes in mindfulness and compassion for others, although it is not designed to determine clinical improvements in mental health. By understanding how pediatric residents engage with different program formats, this study aims to inform the design of more flexible and user-centered digital wellness programs that better fit into demanding medical training environments.",[26,27,28,29,30,31,32,33],"Program Engagement","Treatment Adherence and Compliance","Mindfulness","Self-Compassion","Physician Burnout","Psychological Well-Being","Meditation","Meditation Training",[28,32,35,36,37,38,39,27,40,26,41,42,29,43],"Digital Health Intervention","Internet-Based Intervention","Physician Well-Being","Graduate Medical Education","Pediatric Residency","Patient Acceptance of Health Care","User Engagement","Pilot Projects","Compassion","RECRUITING","2026-05-21",{"date":47,"type":48},"2026-05-26","ACTUAL",{"date":50,"type":48},"2026-04-13",{"date":52,"type":20},"2027-05-01",{"name":54,"class":55},"Northwestern University","OTHER",1,{"id":58,"slug":59,"hasResults":11,"nctId":60,"briefTitle":61,"officialTitle":62,"acronym":4,"eligibilityCriteria":63,"healthyVolunteers":16,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":64,"targetDuration":4,"studyType":21,"phases":66,"briefSummary":67,"conditions":68,"keywords":72,"overallStatus":77,"whyStopped":4,"lastUpdateSubmitDate":78,"lastUpdatePostDateStruct":79,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":84,"locationsCount":4},"100601703","assessing-the-efficacy-and-impact-of-ambient-ai-scribes-in-healthcare-100601703","NCT07113938","Assessing the Efficacy and Impact of Ambient AI Scribes in Healthcare","Assessing the Efficacy and Impact of Ambient AI Scribes in Healthcare: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Physicians from family medicine or any specialty\n* Physicians who regularly see patients in a clinic setting at least 2 days per week\n\nExclusion Criteria:\n\n* Physicians who are planning to leave their practice during the study period",{"count":65,"type":20},64,[23],"The goal of this clinical trial is to assess the impacts of ambient AI scribes on the workload and burnout in physicians who see patients in a clinic setting at least twice in a week, as well as the impacts on patient-physician interaction.\n\nThe main questions it aims to answer are:\n\n* What is the impact of ambient AI scribe use on physician workload and burnout?\n* What is the impact of ambient AI scribe use on quality of patient-physician interaction?\n\nResearchers will compare the group of physicians using the ambient AI scribes to the group not using ambient AI scribes to see if there are any significant differences.\n\nParticipants randomly assigned to Group A will make use of the AI scribe and participants randomly assigned to Group B will not use any AI scribe for the 10 working day duration of the study. They will be asked to complete a survey assessing workload and burnout immediately prior to the commencement of the study and at the end of each week of the study or 5 full working days for part time physicians. They will also invite their patients to complete a survey assessing their experience after each clinical interaction.",[69,70,71,30],"Use of Ambient AI Scribes","Patient-Phyisican Interaction","Physician Workload",[73,74,75,76],"artificial intelligence","physician workload","physician burnout","documentation quality","NOT_YET_RECRUITING","2025-08-02",{"date":80,"type":48},"2025-08-11",{"date":82,"type":20},"2025-08",{"date":82,"type":20},{"name":85,"class":55},"University of Saskatchewan",{"id":87,"slug":88,"hasResults":11,"nctId":89,"briefTitle":90,"officialTitle":91,"acronym":4,"eligibilityCriteria":92,"healthyVolunteers":16,"sex":17,"minAge":93,"maxAge":4,"enrollmentInfo":94,"targetDuration":4,"studyType":21,"phases":96,"briefSummary":98,"conditions":99,"keywords":100,"overallStatus":44,"whyStopped":4,"lastUpdateSubmitDate":106,"lastUpdatePostDateStruct":107,"startDateStruct":109,"completionDateStruct":111,"leadSponsor":113,"locationsCount":56},"100590633","phase-2-evaluating-an-intervention-for-physician-burnout-100590633","NCT06969950","Evaluating an Intervention for Physician Burnout","Evaluating an Evidence-Based Intervention for Physician Burnout","Inclusion Criteria:\n\n1. Being a physician\n2. Able to speak English because all study activities will be conducted in English.\n3. 18+ years\n4. Direct patient care\n\nExclusion Criteria:\n\n1\\. If using psychotropic medication - not on a stable dosage at least 6 weeks","18 Years",{"count":95,"type":20},100,[97],"PHASE2","The goals of this randomized controlled trial are 1) to test the efficacy of an app-based program in reducing physician burnout vs. no app (control) in 100 physicians; 2) to explore the role of an online live training to augment outcomes and develop an ongoing and sustainable support community with a subsample of physicians.",[30],[101,102,103,104,105],"burnout","physicians","app-based","smarthphone","mindfulness","2025-05-09",{"date":108,"type":48},"2025-05-14",{"date":110,"type":48},"2025-02-12",{"date":112,"type":20},"2026-02-27",{"name":114,"class":55},"Brown University"]