A simple letter could ease grief for caregivers after a loved One's death
NCT ID NCT02861625
First seen Jul 08, 2026 · Last updated Jul 09, 2026 · Updated 1 time
Summary
This study tests whether sending a condolence letter to family caregivers after a patient's death, along with offering a bereavement consultation with the doctor, helps them cope better. About 432 caregivers will be randomly assigned to receive either the letter and consultation or standard care. The main goal is to see if this approach improves their mental well-being three months after the loss.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Letter of condolence and post-death medical consultation
- What this could lead to
- If effective, this simple, low-cost approach could become a standard way to support grieving caregivers, potentially reducing prolonged grief and improving quality of life.
- What could go wrong
- The trial is relatively small and measures subjective outcomes like quality of life, which can vary widely. The intervention may not significantly improve well-being compared to standard practice.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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432 people
The number who actually took part.
- Started
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May 2018
- Finished
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Aug 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study population consisted of the reliable person (a family member and/or caregiver, designed by the patient himself at each hospitalization) of cancer patients who have died in one of the participating center.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient died in the institution * Patient for which the reliable person has been identified * Acceptation of the reference physician to send a letter of condolence with the proposed consultation Exclusion Criteria: * The physician already met with the caregiver after the patient's death
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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GRAVIS
Marseille, France
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Institut Paoli Calmettes
Marseille, Bouches Du Rhone, 13009, France
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