Attachment and Post-Traumatic Stress Disorder in Military Personnel: Characterization of the French Military Population, Exploration of Biopsychosocial Factors, and Study of the Impact of Security Priming on Emotional Contagion Capacities
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Attachment and Post-traumatic Stress Disorder in Military Personnel: Characterisation of the French Military Population, Exploration of Biopsychosocial Factors and Study of the Impact of Reassuring Primers on Emotional Contagion Skills.
2 other identifiers
observational
94
0 countries
N/A
Brief Summary
Post-traumatic stress disorder (PTSD) is a pathology that impairs the quality of life of sufferers. In military personnel, it can lead to military incapacity. This psychopathology is characterized by confrontation with one or more traumatic events in the individual's life history. Symptoms include cognitive and mood disorders, avoidance, hyperactivation (hypervigilance and anger) and intrusions (flashbacks and nightmares). Studies show that the prevalence of PTSD in military personnel fluctuates considerably from one situation to another (pre-deployment/post-deployment, etc.). In these at-risk populations, the often more complex PTSD clinic may also account for the heterogeneity of prevalences observed. Nevertheless, PTSD tends to become chronic in military personnel, making it particularly difficult to return to a "previous" state. In French casualties, beyond the symptoms already mentioned, complaints focus on difficulties in social interaction situations involving others in social life (attachment style to others) and in everyday life (public transport, supermarket shopping, social interactions, presence of crowds...). In the context of post-traumatic stress disorder, we would like to explore the processes of social cognition that enable people to interact in their environment, in relation to biological, psychosocial and physiological variables that may constitute risk or maintenance factors for the pathology.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started May 2025
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 21, 2025
CompletedStudy Start
First participant enrolled
May 27, 2025
CompletedFirst Posted
Study publicly available on registry
May 30, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2025
CompletedMay 30, 2025
May 1, 2025
7 months
May 21, 2025
May 21, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
To characterize attachment styles within a military population by comparing a group of military personnel without PTSD (No-PTSD Group) with a group of military personnel with PTSD (PTSD Group).
Our primary outcome measure involves a comparison of the proportions of individuals exhibiting a secure attachment style versus an insecure attachment style (including the subtypes anxious-avoidant, anxious-ambivalent, and disorganized) between the two groups.
One visit study
Study Arms (2)
PTSD-group
military personnel or veterans suffering from PTSD
no PTSD-group
military on active duty without PTSD
Eligibility Criteria
No-PTSD Group: Military personnel without PTSD will be recruited from within an infantry regiment of the army. PTSD Group: Military personnel with PTSD will be recruited during workshops conducted by the CABAT (Cellule d'Aide aux Blessés de l'Armée de Terre - Army Wounded Support Unit) in 2025 and 2026.
You may qualify if:
- Volunteers who agreed to participate in the study and provided written consent
- Affiliated with social security
- Proficient in the French language
- Military personnel diagnosed with post-traumatic stress disorder related to their duties
- Participants in activities offered by the wounded service support units
You may not qualify if:
- Adults subject to a protective measure
- Refusal to participate in the study
- Unrectified Legionnaires
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Biospecimen
Salivary samplings : (i) for the measurement of vasopressin and oxytocin levels , via saliva impregnation by leaving an absorbent (cylindrical cotton) in the mouth for 2 minutes without chewing, and (ii) and for the analysis of genetic polymorphisms, by collecting 2 ml of spit.
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Anaïs Duffaud, PhD
Institut de Recherche Biomédicale des Armées
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 21, 2025
First Posted
May 30, 2025
Study Start
May 27, 2025
Primary Completion
December 31, 2025
Study Completion
December 31, 2025
Last Updated
May 30, 2025
Record last verified: 2025-05
Data Sharing
- IPD Sharing
- Will not share