[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"burnout-professionals\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:burnout-professionals":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,49],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":4},"100637787","development-and-validation-of-single-session-digital-self-guided-intervention-to-prevent-burnout--improve-wellness-100637787",false,"NCT07583420","Development and Validation of Single-Session Digital Self-Guided Intervention to Prevent Burnout & Improve Wellness","Development and Validation of an Evidence-Based, Self-Guided, Single Session Digital Intervention to Prevent Workplace Burnout & Enhance Psychological Wellness","Inclusion Criteria:\n\n* 19 years of age or older\n* Currently employed full-time\n* Reside in Canada\n* Not currently receiving treatment for a significant physical or mental health condition (e.g., ongoing psychotherapy or psychiatric care)\n* Sufficient English proficiency to understand the intervention materials and complete all study assessments\n\nExclusion Criteria:\n\n* Being under 19 years of age\n* Being unemployed, retired, or a student who is not concurrently employed\n* Residing outside Canada\n* Currently engaging in significant mental health treatment",true,"ALL","19 Years",{"count":20,"type":21},250,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study develops and evaluates a self-guided digital single-session mental health intervention designed to reduce workplace burnout and enhance psychological well-being among employed Canadian adults. Workplace burnout, characterized by emotional exhaustion, cynicism, and reduced professional efficacy, affects approximately 40% of Canadian employees and leads to increased absenteeism, reduced productivity, and higher disability claims. Traditional mental health supports face barriers including long wait times, stigma, and accessibility issues. Single-Session Interventions (SSIs) offer a practical, cost-effective, and scalable complement to traditional services.\n\nThis is a randomized, double-arm, online trial. Participants are recruited via Prolific and randomly assigned (1:1) to either the experimental single-session burnout intervention or an active control condition focused on creative writing. The intervention focuses on its unique delivery of content focused on the evidence-based techniques, such as cognitive reframing, stress management, and behavioural strategies. The active control matches the intervention in length, structure, and user experience but omits the specific therapeutic ingredients.\n\nAll procedures are conducted entirely online through Qualtrics. Participants are compensated for their participation. Participants complete three sessions over approximately 30 days:\n\nA baseline survey (about 10 minutes); A program session and immediate follow-up (about 40 minutes); And a 30-day follow-up survey (about 10 minutes).\n\nOutcome measures include burnout (MBI-16), perceived stress (PSS-10), depressive symptoms (PHQ-8), anxiety (GAD-7), general health (GHQ-12), well-being (WHO-5), work engagement (UWES-3), readiness to change, perceived impact, and program feedback\u002Facceptability. Main outcomes are examined using mixed-effects linear regression with a participant-level random intercept to test the group × time interaction across baseline, post-intervention, and follow-up.",[27,28],"Burnout, Professionals","Wellness, Psychological",[30,31,32,33,34,35,36],"Workplace burnout","single-session intervention","self-guided digital intervention","psychological well-being","occupational stress","burnout prevention","employee mental health","NOT_YET_RECRUITING","2026-05-07",{"date":40,"type":41},"2026-05-13","ACTUAL",{"date":43,"type":21},"2026-04",{"date":45,"type":21},"2026-08",{"name":47,"class":48},"Saint Mary's University (Canada)","OTHER",{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":17,"minAge":57,"maxAge":4,"enrollmentInfo":58,"targetDuration":4,"studyType":22,"phases":60,"briefSummary":61,"conditions":62,"keywords":66,"overallStatus":77,"whyStopped":4,"lastUpdateSubmitDate":78,"lastUpdatePostDateStruct":79,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":85,"locationsCount":87},"100616230","ambient-ai-scribe-voa-health-in-outpatient-clinics-draft-notes-documentation-burden-and-well-being-100616230","NCT07302906","Ambient AI Scribe (Voa Health) in Outpatient Clinics: Draft Notes, Documentation Burden, and Well-Being","The SOAR Trial (Scribe Optimization for Ambulatory Records): Ambient Artificial Intelligence Scribe With Voa Health for Generating Medical Documentation From Outpatient Visit Audio - A Randomized Controlled Trial","SOAR","Inclusion Criteria:\n\nPatients:\n\n1. Adults (≥18 years) attended at the participating outpatient clinics of the Hospital de Clínicas - Federal University of Paraná during the study period.\n2. Under the care of a physician participating in the trial.\n3. Ability to understand Portuguese and provide informed consent for the audio recording of the consultation and completion of brief questionnaires.\n4. Ability to complete post-consultation questionnaires during interview.\n\nPhysicians:\n\n1. Resident physicians working in the participating outpatient clinics.\n2. Use of the hospital's electronic medical record in routine care practice.\n3. Agreement to the audio recording of consultations and to the completion of brief questionnaires after each included encounter.\n\nStudent Researchers:\n\n1. Medical students or undergraduate health science students linked to the research project.\n2. Trained in patient registration, collection of Informed Consent (ICF), and administration of questionnaires to the patient on the Infinity Research platform.\n\nExclusion Criteria:\n\n1. Patients under 18 years of age.\n2. Emergency consultations, urgent care, or inpatient care.\n3. Patients with significant cognitive impairment, acute distress, or clinical instability that, in the opinion of the treating physician, precludes providing consent or completing questionnaires, except when accompanied by a legal guardian capable of providing consent on their behalf.\n4. Patients under legal guardianship or who, for any reason, cannot provide consent on their own, except when the guardian or legal representative is present and can provide informed consent.\n5. Consultations where either the patient or the physician refuses audio recording or participation in the study.\n6. Consultations where the AI system is unavailable or malfunctioning (applicable only for protocol adherence analyses).","18 Years",{"count":59,"type":21},300,[24],"The goal of this randomized clinical trial is to learn whether an \"ambient AI scribe\" (Voa Health) can reduce documentation burden and improve physician well-being and patient experience in outpatient clinics. The AI scribe listens to the audio of the consultation and produces a draft of the clinical note that the physician reviews and edits.\n\nIn this study, consultations are randomized to 2 groups: usual documentation (without AI) or documentation assisted by the AI scribe. Adult patients seen in participating clinics, and their physicians, are invited to take part. For both groups, the consultation audio is recorded and, at the end of the visit, physicians and patients complete short questionnaires about well-being, workload, communication, empathy, and satisfaction. The questionnaires are based on internationally used scales (such as PFI, Mini-Z, NASA-TLX, CARE, PSQ-18, and CAT) but adapted to keep them brief and feasible in routine care.\n\nThe main questions are whether the AI scribe lowers the time and effort needed to document the visit, improves physician professional fulfillment and reduces burnout, and whether it affects how patients perceive the communication, empathy, and overall quality of the consultation. No drugs or devices are being tested. The results are expected to guide hospitals on the safe and effective use of ambient AI scribes in real-world clinical practice.",[27,63,64,65],"Medical Records Systems, Computerized","Physician-Patient Relations","Ambulatory Care",[67,68,69,70,71,72,73,74,75,76],"ambient AI scribe","artificial intelligence","clinical documentation","medical note generation","electronic health record","physician well-being","documentation burden","patient experience","outpatient clinics","randomized controlled trial","RECRUITING","2026-03-31",{"date":80,"type":41},"2026-04-01",{"date":82,"type":41},"2025-01-05",{"date":84,"type":21},"2026-06-28",{"name":86,"class":48},"Pedro Angelo Basei de Paula",1]