Mindfulness Training for Medical Personnel
- Conditions
- Burnout, ProfessionalStress
- Interventions
- Behavioral: Mindfulness Booster TrainingBehavioral: Mindfulness-Based Intervention (MBI)Behavioral: Self-Practice
- Registration Number
- NCT03514862
- Lead Sponsor
- University of Miami
- Brief Summary
In this project, the investigators propose to evaluate the impact of a Mindfulness-Based Intervention (MBI) Program on the well-being of University of Miami (UM) clinicians and faculty/staff. If successfully implemented and proven to be effective, this training program may be disseminated to other interested medical personnel.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 74
- Medical faculty, fellows, residents, and other allied healthcare providers at UM Miller School of Medicine and Jackson will be eligible for participation in the study.
- Those not falling into inclusion criteria.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Intervention Mindfulness Booster Training Participants will participate in 4 weeks of the Mindfulness-Based Intervention (MBI) and then will be invited to continue to participate in 4 additional Mindfulness Booster Training. Intervention Mindfulness-Based Intervention (MBI) Participants will participate in 4 weeks of the Mindfulness-Based Intervention (MBI) and then will be invited to continue to participate in 4 additional Mindfulness Booster Training. Control Self-Practice Participants will participate in 4 weeks of the Mindfulness-Based Intervention (MBI) and then continue to Self-Practice for 4 weeks. Control Mindfulness Booster Training Participants will participate in 4 weeks of the Mindfulness-Based Intervention (MBI) and then continue to Self-Practice for 4 weeks.
- Primary Outcome Measures
Name Time Method Change in measure of stress Baseline, 4-weeks, 3-months, 6-months Stress will be measured using the Perceived Stress Scale, a short-form 4 item scale with a range of 0 to 16, with higher scores representing greater stress. Baseline responses will be compared to 4-week assessment responses of the control and intervention groups. Results between the control and intervention groups will be compared for statistical significance.
- Secondary Outcome Measures
Name Time Method Change in measure of burnout Baseline, 4-weeks, 3-months, 6-months Burnout is measured using the 19-item Copenhagen Burnout Inventory including subscales assessing personal burnout, work-related burnout and patient-related burnout. Scores range from 0 to 100. Total score on the scale is the average of the scores on the items with a higher mean representing greater burnout. Baseline responses will be compared to 4-week assessment responses of the control and intervention groups. Results between the control and intervention groups will be compared for statistical significance.
Trial Locations
- Locations (1)
University of Miami Miller School of Medicine
🇺🇸Miami, Florida, United States