Study of Psychosocial and Contextual Determinants of General Practitioners' Management of Burnout

NCT ID: NCT06811181

Last Updated: 2025-02-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

410 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-03-01

Study Completion Date

2028-07-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Burnout

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

CROSS_SECTIONAL

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

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.

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Angers University Hospital

UNKNOWN

Sponsor Role collaborator

National Research Agency, France

OTHER

Sponsor Role collaborator

IGEIA, audit intervention formation recherche en santé, F-44000 Nantes, France

UNKNOWN

Sponsor Role collaborator

Tours university

UNKNOWN

Sponsor Role collaborator

Nantes University Hospital

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

CHU Nantes

Nantes, , France

Site Status

Countries

Review the countries where the study has at least one active or historical site.

France

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Florian OLLIEROU

Role: CONTACT

0240083635 ext. +33

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

RC24_0566

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Ill-health Related Job Loss
NCT03597698 COMPLETED
Risk Management in Primary Care
NCT06484933 NOT_YET_RECRUITING
The POCUS in Practice Study
NCT05696821 COMPLETED NA