Evaluating an app-based program to reduce physician burnout
Evaluating an Evidence-Based Intervention for Physician Burnout
This study is testing whether a mindfulness app can help doctors feel less burned out compared to those who don't use the app.
Quick facts
| Phase | Phase 2 |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Brown University Academic / other |
| Locations | 1 site (Providence, Rhode Island) |
| Trial ID | NCT06969950 on ClinicalTrials.gov |
What this trial studies
This randomized controlled trial aims to assess the effectiveness of an app-based mindfulness training program in alleviating burnout among physicians compared to a control group with no app intervention. The study will involve 100 physicians who will participate in the app-delivered training, with a subset receiving additional online live training to enhance outcomes and foster a supportive community. The trial seeks to provide insights into the potential of digital interventions for improving physician well-being.
Who should consider this trial
Good fit: Ideal candidates for this study are English-speaking physicians aged 18 and older who are directly involved in patient care.
Not a fit: Patients who are currently using psychotropic medication without a stable dosage for at least six weeks may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly reduce burnout levels among physicians, leading to improved mental health and job satisfaction.
How similar studies have performed: Other studies have shown promise in using digital interventions for mental health support, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Being a physician 2. Able to speak English because all study activities will be conducted in English. 3. 18+ years 4. Direct patient care Exclusion Criteria: 1\. If using psychotropic medication - not on a stable dosage at least 6 weeks
Where this trial is running
Providence, Rhode Island
- Brown University — Providence, Rhode Island, United States (Recruiting)
Study contacts
- Principal investigator: Lia Antico, PhD — Brown University
- Study coordinator: Lia Antico, PhD In Neuroscience
- Email: lia_antico@brown.edu
- Phone: +1-401-328-0763
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.