Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT05874362

People Bereaved by Violent Death : Negative Event Biases and Temporal Perception

Led by Hôpital le Vinatier · Updated on 2025-03-06

61

Participants Needed

1

Research Sites

171 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

A violent death is defined by its brutality, unexpectedness and is secondary to an external cause (suicide, homicide, accident). Bereavement following a violent death constitutes a particular clinical situation, at risk of complications. Research on bereavement after a violent death shows higher risks of psychiatric and somatic complications than in bereavement by non-violent death. These complications, sometimes comorbid, take the form of depressive episodes, post-traumatic stress disorders, suicidal behavior and prolonged grief disorders after 12 months, precociously mediated by ruminations. Processes responsible for this increased risk of complications are poorly documented. Current literature relates mainly to socio-demographic and epidemiological factors which, alone, do not explain this difference in risks. Further research is needed exploring other kinds of data and processes. To our knowledge, there is no description of early neurocognitive functioning in people bereaved after violent death. This study aims at exploring early neurocognitive processes which can lead to complications in people bereaved by violent death.

CONDITIONS

Official Title

People Bereaved by Violent Death : Negative Event Biases and Temporal Perception

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Be between 18 and 65 years old
  • Have experienced recent bereavement by violent death of a first- or second-degree relative
Not Eligible

You will not qualify if you...

  • Be a protected adult
  • Not have good mastery of the French language
  • Have a history of neurodegenerative disorder
  • Have a history of psychiatric disorder treated with medication that was changed in the month before the death
  • Have taken benzodiazepine treatment within 24 hours before the first visit (T0)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Hopital Vinatier

Bron, France, 69678

Actively Recruiting

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Research Team

L

Laurene LESTIENNE

CONTACT

V

Véronique VIAL

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

SCREENING

Number of Arms

2

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