- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06774092
Prevalence of Anxiety Symptoms Among French General Practitioners (Psy-MG)
January 8, 2025 updated by: Université de Reims Champagne-Ardenne
Mental health is a major public health issue in the general population, but few studies seem to focus on the mental health of self-employed healthcare professionals, and GPs in particular.
As front-line workers who are often called upon to manage complex situations, they are quite likely to suffer from anxiety-depressive symptoms or burnout.
Nevertheless, general practice is vast, and there are many different ways of practising and organising it.
Study Overview
Detailed Description
The primary objective is to describe the prevalence of clinically significant anxiety symptoms in French self-employed GPs.
The secondary objective is to investigate the factors associated with the presence of clinically significant anxiety symptoms in French self-employed GPs.
Study Type
Observational
Enrollment (Actual)
2000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Reims, France, 51100
- Université de Reims Champagne Ardenne
-
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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
GPs, both qualified and established, practicing in France with at least some self-employed practice, who agreed to take part in the study.
Description
Inclusion Criteria:
- general practitioners
- qualified and established
- practicing in France
- with at least some self-employed practice
- agreeing to participate in the study
Exclusion Criteria:
- salaried general practitioners
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 |
Intervention / Treatment |
|---|---|
|
GPs group
GPs, both qualified and established, practicing in France with at least some self-employed practice, who agreed to take part in the study.
|
Data collection
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
anxiety
Time Frame: Day 0
|
Anxiety will be evaluated using the Scale Trait Anxiety Inventory version Y (STAI-Y-A).
The STAI Form Y-A consists of a set of twenty item sonly focus on the psychological and not the somatic aspects of anxiety.
The STAI Form Y-A is a self-reported questionnaire.
Each item is scored from 1 to 4 and a sum score of all items is computed.
Higher score indicates greater anxiety.
Presence of anxiety will be defined by a score greater than or equal to 46.
|
Day 0
|
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 (Actual)
May 1, 2024
Primary Completion (Actual)
July 1, 2024
Study Completion (Actual)
December 1, 2024
Study Registration Dates
First Submitted
January 8, 2025
First Submitted That Met QC Criteria
January 8, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
January 8, 2025
Last Verified
January 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2024_RIPH_02_Psy-MG
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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