[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"wellness-psychological\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:wellness-psychological":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,8,0,[8,49,70,104,133,156,191,218],{"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":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":16,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":22,"phases":57,"briefSummary":58,"conditions":59,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":69},"100535031","impact-of-a-virtual-reality-based-mindfulness-program-on-clinician-wellness-100535031","NCT06246539","Impact of a Virtual Reality-based Mindfulness Program on Clinician Wellness","Inclusion Criteria:\n\n* physician or APP employed by the Medical Group\n\nExclusion Criteria:\n\n* Not willing to receive 2 texts per week",{"count":56,"type":21},32,[24],"Burnout shares symptoms with anxiety and depression. While there is no single intervention for burnout, there are validated interventions (which are amenable to virtual reality (VR)) for anxiety and depression. UMassMemorial data from the Professional Well-Being Academic Consortium show that MD burnout and distress has increased since 2020. The investigators believe providing clinicians with a unique tool (VR) will be a feasible and efficacious way to tackle distress. It is known that only 1% of our MDs have done mindfulness training but nearly 50% are interested in doing so. Therefore, a self-administrable, interactive mindfulness program delivered over VR has great potential to reach clinicians who want to practice a more active form of mindfulness at a time convenient to them. The results of the study will provide preliminary evidence to determine if a take-home VR mindfulness program decreases clinician stress.",[28],"2026-03-11",{"date":62,"type":41},"2026-03-13",{"date":64,"type":21},"2026-06-01",{"date":66,"type":21},"2028-07-31",{"name":68,"class":48},"University of Massachusetts, Worcester",1,{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":76,"eligibilityCriteria":77,"healthyVolunteers":16,"sex":17,"minAge":78,"maxAge":18,"enrollmentInfo":79,"targetDuration":4,"studyType":22,"phases":81,"briefSummary":82,"conditions":83,"keywords":89,"overallStatus":94,"whyStopped":4,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":98,"completionDateStruct":100,"leadSponsor":102,"locationsCount":69},"100539611","promoting-teenage-sleep-for-improved-mental-health-and-school-performance-100539611","NCT06306092","Promoting Teenage Sleep for Improved Mental Health and School Performance","Promoting Teenage Sleep - for Better Mental Health and School Performance","TeenSleep","Inclusion Criteria:\n\nStudents in Swedish high schools and upper secondary schools.\n\nExclusion Criteria:\n\n\\-","13 Years",{"count":80,"type":21},3000,[24],"The overall aim of this project is to evaluate the effectiveness of two school-based programs that have the potential to promote adolescent sleep and prevent future depressive symptoms. The programs will be offered to students aged 13-19 at Swedish high schools and upper secondary schools at the classroom level. The students will be compared to teaching as usual (control group).",[84,85,86,87,88,28],"Mental Health Issue","Insomnia","Depression","Anxiety","Daytime Sleepiness",[90,91,92,93],"Sleep","Mental health","Adolescents","School-based intervention","RECRUITING","2026-03-03",{"date":97,"type":41},"2026-03-05",{"date":99,"type":41},"2024-08-17",{"date":101,"type":21},"2030-06-30",{"name":103,"class":48},"Kristianstad University",{"id":105,"slug":106,"hasResults":11,"nctId":107,"briefTitle":108,"officialTitle":108,"acronym":109,"eligibilityCriteria":110,"healthyVolunteers":16,"sex":17,"minAge":111,"maxAge":4,"enrollmentInfo":112,"targetDuration":4,"studyType":22,"phases":114,"briefSummary":115,"conditions":116,"keywords":121,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":124,"lastUpdatePostDateStruct":125,"startDateStruct":127,"completionDateStruct":129,"leadSponsor":131,"locationsCount":69},"100578042","the-inspire-study-investigation-of-swiss-physicians-inner-life-resilience-and-emotions-100578042","NCT06806150","The INSPIRE Study: INvestigation of Swiss Physicians Inner-life, Resilience, and Emotions","INSPIRE","Inclusion Criteria:\n\n1. Be a practicing physician in Switzerland\n2. Working at least 40% in a clinical capacity\n3. Be willing and able to provide informed consent\n4. Expecting to be professionally active until 2028\n\nExclusion Criteria:\n\n1. Retired physician or physician seeking retirement within 3 years from first participation in the study\n2. Physician unable to participate in one of the study languages: English, German, or French","18 Years",{"count":113,"type":21},450,[24],"The goal of this clinical trial, nested within an observational cohort study, is to evaluate whether two positive psychology web-based interventions can reduce emotional exhaustion and improve overall well-being in practicing physicians in Switzerland. The main questions it aims to answer are:\n\nDoes participation in positive psychology interventions reduce emotional exhaustion at three months post-intervention? How do these interventions impact physician wellness, job satisfaction, comfort with end-of-life communication and other aspects of physicians' emotional well-being?\n\nResearchers will compare the effects of two intervention arms (general reflection vs. work-specific reflection) to a control group to determine whether focusing on work-specific aspects leads to greater improvements in emotional exhaustion and job-related outcomes.\n\nParticipants will:\n\n* Complete an 8-day intervention consisting of positive psychology activities delivered online.\n* Complete baseline and follow-up assessments over the study period",[117,118,119,28,120],"Burnout, Professional","Emotional Exhaustion","Emotions","Satisfaction, Personal",[122,123],"Psychological resilience","Positive Psychology","2026-02-11",{"date":126,"type":41},"2026-02-13",{"date":128,"type":21},"2026-04-15",{"date":130,"type":21},"2027-08-15",{"name":132,"class":48},"University of Bern",{"id":134,"slug":135,"hasResults":11,"nctId":136,"briefTitle":137,"officialTitle":138,"acronym":4,"eligibilityCriteria":139,"healthyVolunteers":16,"sex":17,"minAge":140,"maxAge":4,"enrollmentInfo":141,"targetDuration":4,"studyType":22,"phases":143,"briefSummary":144,"conditions":145,"keywords":4,"overallStatus":94,"whyStopped":4,"lastUpdateSubmitDate":147,"lastUpdatePostDateStruct":148,"startDateStruct":150,"completionDateStruct":152,"leadSponsor":154,"locationsCount":69},"100550685","effectiveness-of-go-for-transitional-housing-residents-100550685","NCT06450288","Effectiveness of GO for Transitional Housing Residents","Effectiveness of the Green Oasis (GO) Wellness Program for Residents Living in Concordia Tsat Sing Kong Transitional Housing Estate","Inclusion Criteria:\n\n* Aged 10 or above.\n* Scored \\>6 in the Abbreviated Mental Test; a cut-off point of 6 is valid in differentiating between normal and abnormal cognitive functions for geriatric clients.\n* Can understand Cantonese.\n* Able to take part in light exercise and stretching.\n* Have access to smartphone and internet.\n\nExclusion Criteria:\n\n* Have a serious organic disease or malignant tumor.\n* Have a mental disorder diagnosed by neurologists or psychiatrists.\n* Experienced drug addiction","10 Years",{"count":142,"type":21},50,[24],"The goal of this pre-post study is to enhance the health and wellness of the residents in the Concordia Tsat Sing Kong Transitional Housing Estate. This study aims to evaluate the effectiveness of the Green Oasis (GO) wellness program in:\n\n1. Increase health awareness and engaging in health promoting activities, including more physical activities\u002Fwalking, gardening.\n2. Enhance happiness and quality of life.\n\nParticipants will:\n\n* complete physical exercises, gardening, and interact with the GO website\n* receive health talks",[146,28],"Quality of Life","2025-09-10",{"date":149,"type":41},"2025-09-11",{"date":151,"type":41},"2025-01-01",{"date":153,"type":21},"2026-06-30",{"name":155,"class":48},"The Hong Kong Polytechnic University",{"id":157,"slug":158,"hasResults":11,"nctId":159,"briefTitle":160,"officialTitle":160,"acronym":161,"eligibilityCriteria":162,"healthyVolunteers":16,"sex":17,"minAge":163,"maxAge":164,"enrollmentInfo":165,"targetDuration":4,"studyType":167,"phases":4,"briefSummary":168,"conditions":169,"keywords":174,"overallStatus":94,"whyStopped":4,"lastUpdateSubmitDate":183,"lastUpdatePostDateStruct":184,"startDateStruct":185,"completionDateStruct":187,"leadSponsor":189,"locationsCount":69},"100561907","community-park-based-programs-for-health-promotion-the-fit2lead-prospective-cohort-study-100561907","NCT06596265","Community Park-Based Programs for Health Promotion: The Fit2Lead Prospective Cohort Study","F2L","Inclusion Criteria:\n\n* All participants enrolled in the Miami-Dade Fit2Lead study will be included in this secondary analysis\n* Aged 12-17 years, residing in Miami-Dade County\n\nExclusion Criteria:\n\n* Anyone not enrolled in the Miami-Dade Fit2Lead study will be excluded from this secondary analysis\n* Aged \\<12 or \\>17 years, not residing in Miami-Dade County, cannot read and speak in English","12 Years","17 Years",{"count":166,"type":21},1000,"OBSERVATIONAL","The Fit2Lead prospective cohort study examines the effects of a park-based youth mental health and resilience afterschool program on youth participant mental health, resilience, physical fitness, and violence prevention outcomes. Duke will perform a secondary analysis of the data collected as part of the Fit2Lead prospective cohort study run by Miami-Dade County Parks and Recreation.",[87,28,170,171,172,173],"Overweight or Obesity","Hypertension","Prehypertension","Low Physical Fitness",[175,176,177,178,179,180,181,182],"Youth","Adolescent","Afterschool","Parks and Recreation","Mental Health","Physical Helath","Resilience","Violence Prevention","2025-09-03",{"date":147,"type":41},{"date":186,"type":41},"2016-02-17",{"date":188,"type":21},"2028-06-17",{"name":190,"class":48},"Duke University",{"id":192,"slug":193,"hasResults":11,"nctId":194,"briefTitle":195,"officialTitle":196,"acronym":4,"eligibilityCriteria":197,"healthyVolunteers":16,"sex":17,"minAge":111,"maxAge":4,"enrollmentInfo":198,"targetDuration":4,"studyType":22,"phases":200,"briefSummary":201,"conditions":202,"keywords":204,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":209,"lastUpdatePostDateStruct":210,"startDateStruct":212,"completionDateStruct":214,"leadSponsor":216,"locationsCount":69},"100599640","artificial-intelligence-powered-mental-health-support-tool-for-physicians-in-training-100599640","NCT07087119","Artificial Intelligence Powered Mental Health Support Tool For Physicians In Training","A Pilot Study: Exploring The Role Of an Artificial Intelligence Powered Mental Health Support Tool For Mental Health Wellness For Physicians In Training","Inclusion Criteria:\n\n* Individuals 18 years old or older are included.\n* Training physicians in Internal Medicine residency and Gastroenterology fellowship at Cedars Sinai.\n* Study is limited to Cedars-Sinai employees who are known to speak English.\n\nExclusion Criteria:\n\n* Active treatment of severe and uncontrolled anxiety or depression with a health care professional\n* Unwilling and or unable to participate\n* Non-English speakers.",{"count":199,"type":21},20,[24],"The purpose of this pilot study is to evaluate the acceptability of an artificial intelligence powered mental health support tool for mental health wellness amongst physicians in training.\n\nThe primary research procedures are:\n\nThe primary research procedure will be the utilization of artificial intelligence powered mental health support session through a web browser for physicians in training to address symptoms related to depression and anxiety. A pre and post intervention survey, evaluating depression symptoms with the standardized PHQ-9 questionnaire and anxiety symptoms with the standardized GAD-7 questionnaire will be conducted to assess changes in mental health wellness.\n\nThe study will enroll physicians in training, including Internal Medicine residents and Gastroenterology fellows.\n\nThe study includes at least 4 sessions. The total study duration for each subject is 3 months.",[28,203],"Mental Health Wellness 1",[205,206,207,208],"artificial intelligence","physician in training","mental health","wellness","2025-07-17",{"date":211,"type":41},"2025-07-25",{"date":213,"type":21},"2025-07-21",{"date":215,"type":21},"2026-12",{"name":217,"class":48},"Cedars-Sinai Medical Center",{"id":219,"slug":220,"hasResults":11,"nctId":221,"briefTitle":222,"officialTitle":222,"acronym":223,"eligibilityCriteria":224,"healthyVolunteers":16,"sex":17,"minAge":78,"maxAge":225,"enrollmentInfo":226,"targetDuration":4,"studyType":22,"phases":228,"briefSummary":229,"conditions":230,"keywords":4,"overallStatus":94,"whyStopped":4,"lastUpdateSubmitDate":233,"lastUpdatePostDateStruct":234,"startDateStruct":236,"completionDateStruct":238,"leadSponsor":240,"locationsCount":69},"100579305","teen-health-choices--wellness-100579305","NCT06822569","Teen Health Choices & Wellness","THC&W","Inclusion Criteria:\n\n1. be age 13 to 16 years\n2. engage in a target health behavior on at least one recent occasion\n3. speak, read, and understand English or Spanish\n4. live in or near Rhode Island\n\nExclusion Criteria:\n\n1. lifetime history of moderate or severe substance use disorder or treatment, excluding nicotine use disorder\n2. current psychotic symptoms or active suicidality (i.e., intent in the past 30 days)","16 Years",{"count":227,"type":21},224,[24],"The goal of this observational study is to learn more about changes in health, wellness, and substance-use behaviors as teenagers get older. Participants, ages 13 to 16, will be asked to use a smartphone application developed for this research study. Participants will also come to Brown University or meet via video conference to answer questions about specific behaviors, choices, and feelings that may change over time.",[231,28,232],"Health Behavior","Substance Use","2025-03-27",{"date":235,"type":41},"2025-04-02",{"date":237,"type":41},"2024-12-27",{"date":239,"type":21},"2028-02",{"name":241,"class":48},"Brown University"]