- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06112457
Anxiety and Depression Among Gendarmes Posted to French Guiana (TAD-GENDGF)
October 31, 2023 updated by: Direction Centrale du Service de Santé des Armées
Anxiety and Depression Among Gendarmes Posted to French Guiana (TAD-GENDGF)
This is a mixed-method, single-center study involving two concurrent phases: a quantitative phase with an anonymous self-administered questionnaires, and a qualitative phase with individual contextual interviews and a focus group.
The hypothesis underlying this study is that isolated postings are a risk factor for anxiety-depressive disorders.
The aim of this study is to provide new information to help propose targeted prevention and health promotion measures.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
600
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
- Name: DIA
- Phone Number: 0594395983
- Email: aissata.dia@intradef.gouv.fr
Study Locations
-
-
Guyane
-
Cayenne, Guyane, French Guiana, 97306
- DIASS Guyane
-
Contact:
- DIA
- Phone Number: 0594395983
-
-
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
healthy volunteer
Description
Inclusion Criteria:
- Gendarme in active position
- Age over 18
- Assignment in French Guiana for more than 6 months at the time of the study
- Not opting for study participation
Exclusion Criteria:
- Previously diagnosed psychiatric condition
- People with a reading/writing disability in the French language
- Major incapacity
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Prevalence of anxiety-depressive disorders according to posting site.
Time Frame: Through study completion (6 months)
|
Comparison of the prevalence of anxiety-depressive disorders among gendarmes posted to French Guiana according to their posting site.
|
Through study completion (6 months)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Factors associated with the presence of an anxiety-depressive disorder
Time Frame: Through study completion (6 months)
|
Evaluate factors associated with the presence of an anxiety-depressive disorder, both overall and by type of disorder
|
Through study completion (6 months)
|
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)
November 1, 2023
Primary Completion (Estimated)
October 1, 2024
Study Completion (Estimated)
November 1, 2024
Study Registration Dates
First Submitted
October 26, 2023
First Submitted That Met QC Criteria
October 31, 2023
First Posted (Actual)
November 1, 2023
Study Record Updates
Last Update Posted (Actual)
November 1, 2023
Last Update Submitted That Met QC Criteria
October 31, 2023
Last Verified
October 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2022PPRC07
- 2023-100889-36 (Other Identifier: IDRCB)
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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