Study of Psychosocial and Contextual Determinants of General Practitioners' Management of Burnout (BOPEC-MG)

February 5, 2025 updated by: Nantes University Hospital
Burnout is a major public and occupational health issue. Despite accumulated knowledge to date on the determinants of burnout and its treatment, shortcomings when providing support against this complex phenomenon have been found. Although many professionals are involved in the management of burnout, general practitioners (GPs), as primary care providers, are on the front line, and face a range of difficulties that are reflected in the wide variability of medical support brought to the patients. As a result, the diversity of these practices can affect the recovery process of burnout sufferers and their ability to return to work. Deviations from recommended practices can lead to shortcomings in the treatment of burnout. Using an exploratory et descriptive study design, the main objective of BOPEC-MG is to describe the psychosocial mechanisms involved in the management of burnout in general practice that could explain the variation in medical practices.

Study Overview

Status

Not yet recruiting

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:

  1. The contextual aspects of professional practice (e.g. barriers to work);
  2. The attitudes, beliefs and social representations about burnout;
  3. 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:

  1. attitudes
  2. beliefs
  3. social representations
  4. screening for burnout and depression
  5. contextual and environmental psychosocial determinants
  6. care practices
  7. 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

Observational

Enrollment (Estimated)

410

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Nantes, France, 44093
        • CHU Nantes

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Active general practitioners in the northwestern of France (around 23000 GPs)

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

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

Cohorts and Interventions

Group / Cohort
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
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

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:

  1. written judgment on each item,
  2. perfect agreement by the judges as to the unfavorable or favorable value of an item,
  3. 3 out of 4 judges agree that the statement is an attitude or belief. The items selected by this method will constitute the first operational version of the scale.
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

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

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 (Estimated)

March 1, 2025

Primary Completion (Estimated)

November 1, 2025

Study Completion (Estimated)

July 1, 2028

Study Registration Dates

First Submitted

January 30, 2025

First Submitted That Met QC Criteria

February 5, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 5, 2025

Last Verified

January 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • RC24_0566

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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