Effect of Coaching on Surgeon Well-Being, Job Satisfaction, & Fulfillment

Sponsor
Mayo Clinic (Other)
Overall Status
Completed
CT.gov ID
NCT04235751
Collaborator
(none)
80
1
2
17
4.7

Study Details

Study Description

Brief Summary

Researchers are trying to determine if individualized professional coaching improves physicians' sense of well-being and job satisfaction.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Professional Coaching
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
80 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Effect of Coaching on Surgeon Well-Being, Job Satisfaction, & Fulfillment
Actual Study Start Date :
Jan 15, 2020
Actual Primary Completion Date :
Oct 30, 2020
Actual Study Completion Date :
Jun 15, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Immediate Coaching Intervention

Subjects will receive 6 professional coaching sessions

Behavioral: Professional Coaching
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

Behavioral: Professional Coaching
6 individualized professional coaching sessions via phone

Outcome Measures

Primary Outcome Measures

  1. Burnout [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

  2. Job Satisfaction [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

  3. Professional Fulfillment [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

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Surgeons at Mayo Clinic
Exclusion Criteria:
  • Retired surgeons at Mayo Clinic; physicians in other disciplines or organizations

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mayo Clinic Rochester Minnesota United States 55905

Sponsors and Collaborators

  • Mayo Clinic

Investigators

  • Principal Investigator: Liselotte N Dyrbye, MD, Mayo Clinic

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Liselotte (Lotte) N. Dyrbye, Principal Investigator, Mayo Clinic
ClinicalTrials.gov Identifier:
NCT04235751
Other Study ID Numbers:
  • 19-011708
First Posted:
Jan 22, 2020
Last Update Posted:
Jun 16, 2021
Last Verified:
Jun 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 16, 2021