- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04235751
Effect of Coaching on Surgeon Well-Being, Job Satisfaction, & Fulfillment
June 15, 2021 updated by: Liselotte (Lotte) N. Dyrbye, Mayo Clinic
Researchers are trying to determine if individualized professional coaching improves physicians' sense of well-being and job satisfaction.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
80
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Minnesota
-
Rochester, Minnesota, United States, 55905
- Mayo Clinic
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Surgeons at Mayo Clinic
Exclusion Criteria:
- Retired surgeons at Mayo Clinic; physicians in other disciplines or organizations
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: OTHER
- Allocation: RANDOMIZED
- Interventional Model: CROSSOVER
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Immediate Coaching Intervention
Subjects will receive 6 professional coaching sessions
|
6 individualized professional coaching sessions via phone
|
EXPERIMENTAL: Delayed Coaching Intervention
Subjects will receive no coaching for the first six months of the study, at which point they cross over and receive 6 professional coaching sessions
|
6 individualized professional coaching sessions via phone
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Burnout
Time Frame: Baseline, 6 months
|
Change in self-reported Maslach Burnout Inventory (MBI) Score using a scale of never, a few times a year or less, once a month or less, a few times a month, once a week, a few times a week, every day
|
Baseline, 6 months
|
Job Satisfaction
Time Frame: Baseline, 6 months
|
Change in self-reported Physician Job Satisfaction Scale score using a scale of 1=very strongly disagree to 5= very strongly agree
|
Baseline, 6 months
|
Professional Fulfillment
Time Frame: Baseline, 6 months
|
Change in the self-reported Empowerment at Work Scale score using a scale of 1=very strongly disagree to 7=very strongly agree
|
Baseline, 6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Liselotte N Dyrbye, MD, Mayo Clinic
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
January 15, 2020
Primary Completion (ACTUAL)
October 30, 2020
Study Completion (ACTUAL)
June 15, 2021
Study Registration Dates
First Submitted
January 17, 2020
First Submitted That Met QC Criteria
January 17, 2020
First Posted (ACTUAL)
January 22, 2020
Study Record Updates
Last Update Posted (ACTUAL)
June 16, 2021
Last Update Submitted That Met QC Criteria
June 15, 2021
Last Verified
June 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 19-011708
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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