Mindfulness Resiliency Training Pilot for University of Miami Medical Personnel
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- University of Miami
- Enrollment
- 74
- Locations
- 2
- Primary Endpoint
- Change in measure of stress
Study Overview
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.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •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.
Exclusion Criteria
- •Those not falling into inclusion criteria.
Arms & Interventions
Intervention
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 Booster Training (Behavioral)
Intervention
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) (Behavioral)
Control
Participants will participate in 4 weeks of the Mindfulness-Based Intervention (MBI) and then continue to Self-Practice for 4 weeks.
Intervention: Mindfulness Booster Training (Behavioral)
Control
Participants will participate in 4 weeks of the Mindfulness-Based Intervention (MBI) and then continue to Self-Practice for 4 weeks.
Intervention: Self-Practice (Behavioral)
Outcomes
Primary Outcomes
Change in measure of stress
Time Frame: 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 Outcomes
- Change in measure of burnout(Baseline, 4-weeks, 3-months, 6-months)
Investigators
David Lee, PhD
Professor
University of Miami