Clinical Trials Directory

Trials / Terminated

TerminatedNCT01412502

Post Traumatic Stress Among Relatives of Brain-dead, Withdrawal of Life Support, and Sudden Death Patients

Evaluation of Post Traumatic Stress Among the Nearest Relatives of Brain-dead, Withdrawal of Life Support, and Sudden Death Patients

Status
Terminated
Phase
Study type
Observational
Enrollment
119 (actual)
Sponsor
Centre Hospitalier Universitaire de Nīmes · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study concerns the nearest relatives of patients who have passed away within 3 days of admission to an ICU due to: (1) brain death with multiple organ donation +/- tissues or (2) death via limitation and / or cessation of active treatment (LATA) without brain death or (3) sudden death of a previously healthy patient (no physical or mental limitations; MacCabe score = 0) within 3 days of admission to ICU without LATA nor brain death. Our primary objective is to determine the proportion of nearest relatives at risk for post traumatic stress disorder as defined by an Impact of Event Scale score greater than 37, and to compare this factor between the three above-mentioned groups.

Conditions

Interventions

TypeNameDescription
OTHERIES-R and HDAS scoresThe Impact of Event Scale and Hospital Depression and Anxiety Score questionnaires are administered to participants.

Timeline

Start date
2012-06-15
Primary completion
2016-06-28
Completion
2016-06-28
First posted
2011-08-09
Last updated
2018-01-03

Locations

6 sites across 1 country: France

Source: ClinicalTrials.gov record NCT01412502. Inclusion in this directory is not an endorsement.