The Impact of Professional Coaching on Early Career Academic Emergency Physicians

January 4, 2021 updated by: Richard C Winters, Mayo Clinic

The Impact of Professional Coaching on Early Career Academic Emergency Physician Well-Being, Burnout, Leadership Strengths, and Goal Attainment: A Pilot Randomized, Controlled Trial

This research study is designed to answer the question: How does professional coaching impact early career academic emergency medicine physician goal attainment, leadership strengths, well-being, and burnout?

Study Overview

Detailed Description

A recent systematic review and meta-analysis found coaching to have significant positive effects on goal attainment, well-being, coping skills, work attitudes, and goal-directed self-regulation. Randomized controlled studies of professional coaching have found significant positive effects in various settings including high school teachers and students, postgraduate students in a major university, and executives in the commercial, government, and education sectors.

Coaching provides the participant focused time with a trained professional who facilitates that participant's self-determined and self-directed problem-solving and change. Coaching helps the participant "get on the balcony" away from the action on the "dance floor" to see things from a different and broader perspective and, in doing so, enriches the participant's ability to generate options, challenge biases, understand the effects of emotions, and consider uncertainty.

This study also establishes the level of adult development of academic faculty and creates an initial qualitative dataset for further longitudinal study and theory generation for physician well-being, burnout, leadership strengths, and goal attainment.

Study Type

Interventional

Enrollment (Actual)

46

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 in Rochester

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion:

  • Emergency physicians
  • Academic appointment of Instructor or Assistant Professor
  • Work greater than 80% of their time in a residency and fellowship program approved by the Accreditation Council of Graduate Medical Education (ACGME), the American Osteopathic Association (AOA), or the Royal College of Physicians and Surgeons of Canada (RCPSC) will be invited to participate in the study.

Exclusion:

  • Mayo Clinic emergency physicians are not eligible for this study.

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: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: One-to-One Coaching

Participants randomized to One-to-One Coaching meet for an initial 2-hour coaching session, followed by seven 1-hour coaching sessions every 3-weeks. These eight sessions take place over the course of 6 months.

Additional requirements for One-to-One Coaching:

  • Complete a 30-minute online assessment of goal attainment, well-being, burnout, and leadership strengths (a) at study enrollment, (b) at 6-months after study enrollment, and (c) 12-months following study enrollment.
  • Complete a 15-minute VIA Character Strengths Test online prior to One-to-One Coaching.
  • Following the completion of the final coaching session, participants are interviewed by a con-investigator by phone call to assess the experience of coaching.

Each coaching session will be recorded, transcribed, anonymized, and analyzed to identify common themes.

Professional coaching is provided by the Principal Investigator via video conference.
Other Names:
  • Coaching
Active Comparator: Group Coaching

Participants meet for 90-minutes each month for 6 months for facilitated professional coaching with a group of colleagues.

Additional requirements:

  • Complete a 30-minute online assessment of goal attainment, well-being, burnout, and leadership strengths (a) at study enrollment, (b) at 6-months after study enrollment, and (c) 12-months following study enrollment.
  • Complete a 15-minute VIA Character Strengths Test online prior to Group Coaching.
  • Prior to your initial group coaching session, participate in a 75-minute private phone interview with the primary investigator to discuss the how you make decisions and make sense of the world.
  • Following the completion of the final coaching session, participants are interviewed by a con-investigator by phone call to assess the experience of coaching.

Each coaching session will be recorded, transcribed, anonymized, and analyzed to identify common themes.

Professional coaching is provided by the Principal Investigator via video conference.
Other Names:
  • Coaching
No Intervention: Group Coaching Waitlist

Participants are offered group coaching at the completion of the 12-month study period. Six 90-minute group coaching sessions will occur over the course of six months.

Additional requirements:

• Complete a 30-minute online assessment of goal attainment, well-being, burnout, and leadership strengths (a) at study enrollment (b) and at 6-months after study enrollment.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Goal Setting and Attainment
Time Frame: 18 months (3 measurements at 6-month intervals)
Each participant identifies two professional goals at study onset. For each of the goals, participants respond to the question, "Up to today, how successful have you been in achieving this goal?" and rate their goal attainment on a scale from 0% (no attainment) to 100% (complete attainment). To control for differences between participants in perceived goal attainment difficulty, participants also will rate each goal for perceived difficulty on a 4-point scale ( 1=very easy, 2=somewhat easy, 3=somewhat difficult, 4=very difficult). Goal attainment scores are calculated by multiplying the difficulty rating by the degree of success.
18 months (3 measurements at 6-month intervals)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Psychological Well-Being Scale
Time Frame: 18 months (3 measurements at 6-month intervals)
An 18-item survey that measures eudaemonic well-being.
18 months (3 measurements at 6-month intervals)
Empowerment at Work Scale
Time Frame: 18 months (3 measurements at 6-month intervals)
A 12-item survey that measures a physician's sense of meaning, competence, self-determination, and impact while at work.
18 months (3 measurements at 6-month intervals)
Abbreviated Two-Item Maslach Burnout Inventory
Time Frame: 18 months (3 measurements at 6-month intervals)
A two-item survey that measures participant burnout.
18 months (3 measurements at 6-month intervals)
Depression, Anxiety, and Stress Scale (DASS 21)
Time Frame: 18 months (3 measurements at 6-month intervals)
A 21-item self-report questionnaire designed to measure the severity of the core symptoms of depression, anxiety, and stress in both clinical and nonclinical scenarios.
18 months (3 measurements at 6-month intervals)
Leadership Self-Efficacy Scale
Time Frame: 18 months (3 measurements at 6-month intervals)
A 5-item scale of leadership self-efficacy.
18 months (3 measurements at 6-month intervals)
Self-Insight Scale
Time Frame: 18 months (3 measurements at 6-month intervals)
An 8-item sub-scale of the Self-reflection and Insight Scale. This scale measures individuals' levels of insight into their thoughts, feelings and behaviors.
18 months (3 measurements at 6-month intervals)
Solution-Focused Thinking Scale
Time Frame: 18 months (3 measurements at 6-month intervals)
A 12-item scale with three subscales: Problem Disengagement, Goal Orientation, and Resource Activation.
18 months (3 measurements at 6-month intervals)
Tolerance for Ambiguity Scale
Time Frame: 18 months (3 measurements at 6-month intervals)
An eight-item assessment that measures tolerance for ambiguity.
18 months (3 measurements at 6-month intervals)
Perspective Taking Scale
Time Frame: 18 months (3 measurements at 6-month intervals)
A 7-item subscale of The Empathy Questionnaire that measures perspective-taking.
18 months (3 measurements at 6-month intervals)
Qualitative Summary of Coaching Program
Time Frame: After 6-month coaching intervention. 18 months
An open-ended interview covering issues such as 1) participant's experience with the coaching process and coach; 2) participant goals; 3) impact on the participant's workplace; 4) impact on participant's personal life; and 5) what the participant plans to do to sustain any changes or learnings.
After 6-month coaching intervention. 18 months
Subject-Object Interview
Time Frame: 18 months
A one-time 60 to 75-minute private interview that measures the particpant's order of subject-object development based upon constructive-developmental theory.
18 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Principal Investigator: Richard C Winters, 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.

General Publications

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)

June 1, 2017

Primary Completion (Actual)

March 5, 2020

Study Completion (Actual)

March 5, 2020

Study Registration Dates

First Submitted

April 12, 2017

First Submitted That Met QC Criteria

April 19, 2017

First Posted (Actual)

April 24, 2017

Study Record Updates

Last Update Posted (Actual)

January 6, 2021

Last Update Submitted That Met QC Criteria

January 4, 2021

Last Verified

January 1, 2021

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

We may make anonymized individual participant data (IPD) available to other researchers. It may be available after the completion of the trial to those who contact the PI directly.

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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