Effect of a Life Coaching Intervention on the Well-being and Distress of Physicians

Sponsor
Ottawa Hospital Research Institute (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05149911
Collaborator
Canadian Anesthesiologists' Society (Other), University of Ottawa (Other)
90
1
2
9
10

Study Details

Study Description

Brief Summary

There is a widespread epidemic of distress and burnout (i.e., extreme distress) among Canadian physicians. Burnout is costly to physicians, patients, and healthcare organizations as it compromises physicians' own health and reduces their capacity to deliver high quality, safe care to patients. Life coaching delivered by certified coaches is a personal development tool. Life coaching has been proven to help individuals maximize their strengths and skills to handle stressors, regain control over their lives, act according to their core values, and achieve their full potential, consequently reducing their vulnerability to burnout. The investigators will evaluate life coaching for physicians' well-being in the current Canadian context. Physicians from centres in Canada will be randomly assigned to life coaching (intervention) or no coaching (control) group. The coaching group will receive a 1-hour initial coaching session followed by five 30-minute coaching sessions occurring at a frequency of every 2 to 3 weeks within 5 months (total of 3.5 coaching hours). All coaching sessions will be delivered virtually by certified life coaches. The investigators will assess the impact of coaching on physician distress and quality of life before and after the intervention.

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

Study Design

Study Type:
Interventional
Anticipated Enrollment :
90 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Effect of a Life Coaching Intervention on the Well-being and Distress of Physicians: A Randomized Clinical Trial
Anticipated Study Start Date :
Jun 1, 2022
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Mar 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Coaching

Participants randomized to the coaching group will receive a 1-hour initial professional coaching session followed by five 30-minute professional coaching sessions occurring at a goal frequency of every 2 to 3 weeks within 5 months (total of 3.5 coaching hours). All coaching sessions will be conducted individually (i.e. between one coach and one participant). Participants will be able to request coaching on any topic to individualize the intervention, but the general structure of the sessions will be standardized across participants. All coaching sessions will be performed over the phone or virtual web meeting as standard in coaching practices.

Behavioral: Life Coaching
Sessions with a professional life coach.

No Intervention: Control

Participants randomized to the control group will receive "no intervention" but will be asked to complete the distress and wellness survey at the same time points as participants in the intervention group. Participants in the control group will receive the life coaching intervention after the statistical analysis is completed.

Outcome Measures

Primary Outcome Measures

  1. Change in Quality of Life score at 5 months [5 months]

    Assessed using the reduced version of the World Health Organization (WHO) Quality of Life (QOL) questionnaire (WHOQOL-BREF), one of the most widely used questionnaires for assessing adult QOL, including among healthcare professionals.

Secondary Outcome Measures

  1. Change in Burnout score at 5 months [5 months]

    Measured using the Maslach Burnout Inventory. Minimum score 0, maximum score 132. A higher score is worse, i.e., more burnout.

  2. Change in Resilience score at 5 months [5 months]

    Measured using the Connor-Davidson Resilience Sale. Minimum score 0, maximum score 100. A higher score is better, i.e., more resilience.

  3. Change in Job Satisfaction score at 5 months [5 months]

    Measured using the Global Job Satisfaction subscale of the Physician Job Satisfaction Scale. Minimum score 12, maximum score 60. A higher score is better, i.e., more satisfied.

  4. Change in Job Engagement score at 5 months [5 months]

    Measured using the Utrecht Work Engagement Scale. Minimum score 0, maximum score 102. A higher score is better, i.e., better engagement.

  5. Change in Job Empowerment and Meaning score at 5 months [Baseline and 5 months]

    Measured using the Empowerment at Work Scale. Minimum score is 12, maximum score is 84. A higher score is better, i.e., higher empowerment.

  6. Absence from work due to mental or physical illness [Baseline]

    Measured as the number of days reported by participants.

  7. Absence from work due to mental or physical illness [5 months]

    Measured as the number of days reported by participants.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Registered staff physician, resident, or fellow

  • Currently practicing in Ontario in primary or acute care

Exclusion Criteria:
  • Previously received life coaching in the last 5 years

  • Currently receiving another form of wellness intervention (e.g., psychotherapy)

Contacts and Locations

Locations

Site City State Country Postal Code
1 The Ottawa Hospital Ottawa Ontario Canada K1Y4E9

Sponsors and Collaborators

  • Ottawa Hospital Research Institute
  • Canadian Anesthesiologists' Society
  • University of Ottawa

Investigators

  • Principal Investigator: Sylvain Boet, MD, PhD, The Ottawa Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ottawa Hospital Research Institute
ClinicalTrials.gov Identifier:
NCT05149911
Other Study ID Numbers:
  • 20210617-01H
First Posted:
Dec 8, 2021
Last Update Posted:
Apr 20, 2022
Last Verified:
Apr 1, 2022
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 Apr 20, 2022