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CONDOL01: Evaluation on the Experience of Bereavement, of a Medical Consultation, Proposed by a Letter of CONDOLence to the Patients' Relatives Versus Standard Practice After the Death of the Patient — CONDOL01  

Caregivers Clinical Trial

Official title:
CONDOL01: Evaluation on the Experience of Bereavement, of a Medical Consultation, Proposed by a Letter of CONDOLence to the Patients' Relatives Versus Standard Practice After the Death of the Patient: A Multicenter, Randomized Trial

Clinical Trial Summary

The aim of this randomized multicenter study is to evaluate the impact in offering the condolence letter to the family caregivers (indicated as the reliable person by the patient himself at each hospitalization) and a bereavement consultation with the reference physician.

Clinical Trial Description

The hypothesis is that offering the opportunity to clarify questions about the patients' terminal care will influence positively the grieving process. In particular, the study team hypothesized that psychological morbidity will be reduced (main objective) as well as some aspects of QOL (secondary objective). It is also assumed that the situations of conflict (solicitations for medical records, number of legal procedures) will be reduced. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02861625
Study type Observational
Source Institut Paoli-Calmettes
Contact Dominique Genre, MD
Phone 0033491223778
Email drci.up@ipc.unicancer.fr
Status Recruiting
Phase
Start date May 24, 2018
Completion date June 4, 2022
View Details
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