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Mindfulness Training for Medical Personnel

Not Applicable
Completed
Conditions
Burnout, Professional
Stress
Interventions
Behavioral: Mindfulness Booster Training
Behavioral: 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
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.
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Exclusion Criteria
  • Those not falling into inclusion criteria.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
InterventionMindfulness Booster TrainingParticipants 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.
InterventionMindfulness-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.
ControlSelf-PracticeParticipants will participate in 4 weeks of the Mindfulness-Based Intervention (MBI) and then continue to Self-Practice for 4 weeks.
ControlMindfulness Booster TrainingParticipants will participate in 4 weeks of the Mindfulness-Based Intervention (MBI) and then continue to Self-Practice for 4 weeks.
Primary Outcome Measures
NameTimeMethod
Change in measure of stressBaseline, 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
NameTimeMethod
Change in measure of burnoutBaseline, 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

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