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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

NCT02861625 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 432

Last updated 2020-01-10

No results posted yet for this study

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.

Conditions

  • Caregivers

Interventions

BEHAVIORAL

Letter of condolence and post-death medical consultation

Process of sending a letter of condolence with consultation proposition.

Sponsors & Collaborators

  • Institut Paoli-Calmettes

    lead OTHER

Principal Investigators

  • Gwenaelle Gravis, MS · Institut Paoli-Calmettes

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-05-24
Primary Completion
2022-06-04
Completion
2022-06-04

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02861625 on ClinicalTrials.gov