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Clinical Trial Summary

The main objective of this study is to compare the rate of reported anxiety / depression (HADS >= 8) among spouses and other family members in ICU patients.


Clinical Trial Description

The secondary objectives of this study are:

- to assess symptoms of anxiety (HADS ≥ 8) and depression (HADS ≥ 8) among relatives of ICU patients three months after discharge

- to assess what relatives felt vis-à-vis the information process

- describe the number and duration of interviews with participants

- to compare variables between the groups "spouses" and "other relatives".

- satisfaction

- number and duration of interviews

- HADS questionnaire

- The scale Edmunton

- an internal questionnaire

- IES-R score

- level of mental well-being: WEMWBS

- to describe the completeness of the study

- to test the hypothesis that the development of symptoms related to physical manifestations of anxiety and depression predicts the development of post-traumatic stress at 3 months.

- to assess the impact of the various forms of stress during hospitalization. ;


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT01589575
Study type Observational
Source Centre Hospitalier Universitaire de Nimes
Contact
Status Completed
Phase N/A
Start date September 2012
Completion date January 2015

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