Intervention Trial to Increase Meaning in Work and Reduce Burnout
Primary Purpose
Burnout, Professional
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Small group meetings (COMPASS: COlleagues Meeting to Promote And Sustain Satisfaction)
Sponsored by
About this trial
This is an interventional treatment trial for Burnout, Professional focused on measuring well-being, burnout
Eligibility Criteria
Inclusion Criteria:
- Senior Associate Consultants and Consultants in the Mayo Clinic Department of Medicine will be eligible for this study.
Exclusion Criteria:
- None beyond inclusion criteria.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Small group intervention
Control
Arm Description
Those randomized to the immediate intervention arm will be asked to meet approximately every other week for 6 months, covering 12 sessions. We will ask each group to meet in a relatively private setting (e.g., a restaurant near campus or a reserved meeting room), rather than more public spaces (e.g. river room, cafeteria) where interruptions are more likely.
Participants randomized to Arm 2 (delayed intervention) will be "wait listed" to begin sessions 6 months after the start of the study. This participation will be optional.
Outcomes
Primary Outcome Measures
Burnout
Maslach Burnout Inventory results
Secondary Outcome Measures
Depressive symptoms
PRIME-MD
Quality of life
LASA QOL
Job satisfaction
PJSS
Meaning at work
EWS
Social support
Social Provisions Scale
Social isolation
PROMIS Social Isolation
Job turnover
Single item asking about 2-year plans to leave current practice
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04466423
Brief Title
Intervention Trial to Increase Meaning in Work and Reduce Burnout
Official Title
Intervention Trial Designed to Promote Collegiality and Mutual Support at Work as a Way to Increase Meaning in Work and Reduce Burnout
Study Type
Interventional
2. Study Status
Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
September 1, 2013 (Actual)
Primary Completion Date
October 1, 2014 (Actual)
Study Completion Date
October 1, 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mayo Clinic
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Collegiality is a one of the great virtues of physician-hood. Mutual support from colleagues to help deal with the challenges of being a physician has long helped physicians manage the stress related to practicing medicine and helped physicians derive meaning from their work. Unfortunately, increased productivity expectations and other changes to the practice of medicine over the last several decades have decreased the time physicians have to interact with colleagues and eroded the fabric of collegiality. Recent studies suggest burnout affects nearly half of U.S. physicians at any given point in time and has substantial personal and professional consequences. The steps organizations can take to promote collegiality are unknown. The goal of the present study is to evaluate the ability of an organizational intervention to encourage collegiality, shared experience, connectedness, and mutual support. This study builds on two prior intervention studies directed by the Mayo Clinic Department of Medicine Program on Physician Well-Being, the first focusing on a small group facilitated well-being curriculum and the second focusing on individual electronic tasks to prompt positive reflection and gratitude.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Burnout, Professional
Keywords
well-being, burnout
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Two-arm randomized controlled trial
Masking
Outcomes Assessor
Masking Description
Groups labeled "1" or "2" with random order assignment.
Allocation
Randomized
Enrollment
125 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Small group intervention
Arm Type
Experimental
Arm Description
Those randomized to the immediate intervention arm will be asked to meet approximately every other week for 6 months, covering 12 sessions. We will ask each group to meet in a relatively private setting (e.g., a restaurant near campus or a reserved meeting room), rather than more public spaces (e.g. river room, cafeteria) where interruptions are more likely.
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
Participants randomized to Arm 2 (delayed intervention) will be "wait listed" to begin sessions 6 months after the start of the study. This participation will be optional.
Intervention Type
Behavioral
Intervention Name(s)
Small group meetings (COMPASS: COlleagues Meeting to Promote And Sustain Satisfaction)
Intervention Description
The first 15 minutes of each session will be semi-structured discussion involving i) check in and ii) dialogue about the assigned question. Group leaders will be provided 3-4 discussion questions for each session. The group (or the leader) can choose the one they are most interested in and will then spend 10-15 minutes discussing the question together. Questions will touch on key themes for discussion (see the attached topics list) and are derived from our previous intervention studies. The remainder of the time can be used for socializing and building relationships with colleagues.
Primary Outcome Measure Information:
Title
Burnout
Description
Maslach Burnout Inventory results
Time Frame
12 month outcomes
Secondary Outcome Measure Information:
Title
Depressive symptoms
Description
PRIME-MD
Time Frame
12 month outcomes
Title
Quality of life
Description
LASA QOL
Time Frame
12 month outcomes
Title
Job satisfaction
Description
PJSS
Time Frame
12 month outcomes
Title
Meaning at work
Description
EWS
Time Frame
12 month outcomes
Title
Social support
Description
Social Provisions Scale
Time Frame
12 month outcomes
Title
Social isolation
Description
PROMIS Social Isolation
Time Frame
12 month outcomes
Title
Job turnover
Description
Single item asking about 2-year plans to leave current practice
Time Frame
12 month outcomes
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Senior Associate Consultants and Consultants in the Mayo Clinic Department of Medicine will be eligible for this study.
Exclusion Criteria:
None beyond inclusion criteria.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Colin West, MD
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
34366134
Citation
West CP, Dyrbye LN, Satele DV, Shanafelt TD. Colleagues Meeting to Promote and Sustain Satisfaction (COMPASS) Groups for Physician Well-Being: A Randomized Clinical Trial. Mayo Clin Proc. 2021 Oct;96(10):2606-2614. doi: 10.1016/j.mayocp.2021.02.028. Epub 2021 Aug 5.
Results Reference
derived
Links:
URL
https://www.mayo.edu/research/clinical-trials
Description
Mayo Clinic Clinical Trials
Learn more about this trial
Intervention Trial to Increase Meaning in Work and Reduce Burnout
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