- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06811181
Study of Psychosocial and Contextual Determinants of General Practitioners' Management of Burnout (BOPEC-MG)
Study Overview
Status
Conditions
Detailed Description
The principal aim of this interdisciplinary project is to conduct an exploratory study of GPs' attitudes, beliefs and social representations with regard to burnout management, in order to better understand how their perceptions of this syndrome can influence their practices.
A mixed method combining qualitative and quantitative data collection will be used with samples from the French GPs population.
In phase 1 (qualitative study), semi-structured interviews will be conducted to explore:
- The contextual aspects of professional practice (e.g. barriers to work);
- The attitudes, beliefs and social representations about burnout;
- Concrete practices for managing burnout (e.g. prescribing sick leave).
In addition to semi-structured interviews, qualitative data collection will include the examination of fictional clinical cases to describe medical practices. The format of the four fictional will be video, with actors playing the roles of patients with severe burnout in general practice. The independent variables manipuled will be age and gender.
In phase 2 (quantitative study), a questionnaire will be sent to french general practitioners. it will include scales developed using the results of phase 1 and scales validated by the scientific literature.
As for quantitative data collection, in addition to scales dedicated to attitudes, beliefs and practices, a questionnaire will include a free association task to describe social representations of burnout.
the questionnaire will measure:
- attitudes
- beliefs
- social representations
- screening for burnout and depression
- contextual and environmental psychosocial determinants
- care practices
- socio-demographic variables
A randomized controlled trial aimed at harmonizing practices in general practice could be carried out on the basis of the results. Furthermore, the applications of the present study will be twofold: designing training courses in burnout management for the medical population, and contributing to communication campaigns to encourage GPs to follow the recommendations.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Florian OLLIEROU
- Phone Number: +33 0240083635
- Email: florian.ollierou@chu-nantes.fr
Study Locations
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Nantes, France, 44093
- CHU Nantes
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- practicing GPs
- GPs in northwestern region of France
- GPs with regular use of sick leave prescriptions
Exclusion Criteria:
- GPs with particular mode of exercise (e.g. 100% homeopathy)
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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General practitioners
Only practising French GPs will be included in the study. In qualitative phase, each GP will be interviewed during a research interview lasting one to one-and-a-half hours. In quantitative phase, GPs will receive an e-mail with a link to complete the questionnaire. The survey will take 15 minutes to complete. For the inclusion of participants in the qualitative phase, the sampling method chosen is that of maximum variation. The criteria used are: gender, age, seniority, type of agreement, type of territory, type of work organization. The quantitative phase involves sending a questionnaire by email to a professional mailing list of general practitioners. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Attitudes and beliefs about burnout will be assessed with scales developed specifically on the basis of the qualitative results.
Time Frame: 1 day. Each participant is assessed one time
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Attitude and belief scales will include a series of items and statements relating to burnout and its management. The measurement method chosen is the Lickert scale, classically used for attitude assessment. The items and statements will be based on the content of the interviews (qualitative phase). The items will be subjected to a 3-stage judges' validation test:
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1 day. Each participant is assessed one time
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Social representations about burnout will will be assessed with a free association test (Vergès, Scanon & Junique, 2005).
Time Frame: 1 day. Each participant is assessed one time
|
The free association task is the method traditionally used to measure social representations. It consists in proposing an inductive word and asking the participant to evoke the 5 words related to this inductive term. This procedure has the advantage of being quick and encouraging spontaneity, which favors less controlled responses than in a qualitative survey. (Guimelli & Abric, 2007). In the context of this research, the inducer words will be: "burnout", "sick leave", "general practitioner". |
1 day. Each participant is assessed one time
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- RC24_0566
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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