Burn Out Among Medical Family Doctors
BOUM
Study of the Prevalence, Risk Factors and Protective Factors of Burnout Among General Practitioners in France
1 other identifier
observational
1,536
1 country
1
Brief Summary
The main objective of this study is to assess the burnout prevalence among French general practitioners in private practice. As secondary outcomes, this study aim to measure the impact of sociodemographic variables, organizational practice models and workload. the investigators also intend to characterize the prevalence of depression, anxiety, fatigue and stress, drugs and alcohol consumption, use of psychotropic medication, and preferred strategies to cope with their symptoms.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Nov 2016
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 1, 2016
CompletedFirst Submitted
Initial submission to the registry
January 22, 2020
CompletedFirst Posted
Study publicly available on registry
January 27, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2022
CompletedJanuary 27, 2020
January 1, 2020
4.6 years
January 22, 2020
January 24, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Burnout in French General Practitioners
To evaluate the burnout prevalence in French General Practitioners, using the Maslach Burn-Out Inventory questionnaire
Day 1
Secondary Outcomes (7)
Anxiety
Day 1
Depression
Day 1
Stress
Day 1
Fatigue
Day 1
sleep disturbance
Day 1
- +2 more secondary outcomes
Eligibility Criteria
General practitioners working in France
You may qualify if:
- General practitioners working in France
You may not qualify if:
- None
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CHU Clermont Ferrand
Clermont-Ferrand, Auvergne, 63000, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Frederic Dutheil
University Hospital, Clermont-Ferrand
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 22, 2020
First Posted
January 27, 2020
Study Start
November 1, 2016
Primary Completion
June 1, 2021
Study Completion
June 1, 2022
Last Updated
January 27, 2020
Record last verified: 2020-01