Clinical Trials Directory

Trials / Unknown

UnknownNCT02861625

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: 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

Status
Unknown
Phase
Study type
Observational
Enrollment
432 (estimated)
Sponsor
Institut Paoli-Calmettes · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
BEHAVIORALLetter of condolence and post-death medical consultationProcess of sending a letter of condolence with consultation proposition.

Timeline

Start date
2018-05-24
Primary completion
2022-06-04
Completion
2022-06-04
First posted
2016-08-10
Last updated
2020-01-10

Locations

2 sites across 1 country: France

Source: ClinicalTrials.gov record NCT02861625. Inclusion in this directory is not an endorsement.