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NCT05620381 Clinical Trial

Health and Sleep Assessment After the Strasbourg Attacks of December 11, 2018

Stress Disorders, Post-Traumatic Clinical Trial

— ELSSAS  

Official title:
Health and Sleep Assessment After the Strasbourg Attacks of December 11, 2018

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05620381
Other study ID # 7713
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 9, 2020
Est. completion date December 31, 2023

Study information
Verified date November 2022
Source University Hospital, Strasbourg, France
Contact Amaury MENGIN, MD
Phone 33 3 88 11 57 70
Email amaury.mengin@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Evaluation of the prevalence of post-traumatic stress disorder (PTSD), associated risk factors, health care consumption, and sleep disorders in a civilian population exposed to the December 11, 2018, attacks in Strasbourg. Terrorist attacks have unfortunately become all too frequent on our territory in recent years. A better knowledge of the psychological and psychiatric repercussions on exposed populations is essential in order to better prevent and treat disorders that can have a major functional impact on the lives of exposed individuals and to adapt care during future similar events

Recruitment information / eligibility
Status Recruiting
Enrollment 300
Est. completion date December 31, 2023
Est. primary completion date December 2023
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria: - Major subject (= 18 years old), - Having been exposed to the attacks of December 11, 2018 in Strasbourg directly or indirectly (presence at the scene or close relative present at the scene) - Subject who has not expressed his opposition, after information, to the reuse of his data for the purpose of this research Exclusion Criteria: - Subject who has expressed opposition to participating in the study - Subject under guardianship, curatorship or legal protection

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France Service de Psychiatrie d'Urgences, de Liaison et de Psychotraumatologie - CHU de Strasbourg - France Strasbourg

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Retrospective evaluation of the prevalence of post-traumatic stress disorder (PTSD) in a population exposed to the attacks of December 11, 2018 in Strasbourg Files analysed retrospectively from February 11, 2018 to November 30, 2019 will be examined
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