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Clinical Trials/NCT02325297
NCT02325297CompletedNot Applicable

"Impacts of the Letter of Condolence to the Bereaved Families Experience After a Death in ICU " - Study Famirea 22

Assistance Publique - Hôpitaux de Paris1 site in 1 country242 target enrollmentStarted: December 1, 2014Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
242
Locations
1
Primary Endpoint
HADS (Hospital Anxiety and Depression Scale)

Study Overview

Brief Summary

After the death of a patient in the hyper-technical context of intensive care, his relatives are particularly vulnerable and often exhibit symptoms of anxiety, depression, post traumatic stress and complicated grief. The first results of a qualitative study Famiréa current (CAESAR) support the idea that the bereaved relatives suffer from persistent misunderstandings and a feeling of abandonment of the resuscitation team. Many families suggest the need for contact with the team after the patient's death. The letter of condolence received by some families allowed them to feel recognized in their pain resuscitation teams. This has led us to ask the question of post-death monitoring and interest to send to bereaved relatives a letter of condolence, as recommended by the American consensus conference in 2004 on good palliative care. This strategy would allow the recognition of both close to the pain but also the strong bond that united the resuscitation team. The hypothesis of the study is that the post-death followed in the form of a letter of condolence sent by the intensive care physician who was in charge of the patient, could reduce the risk of having symptoms of anxiety / depression and post-traumatic stress and reduce the rate of complicated grief.

Famirea 22 is randomized clinical trial aimin to compare two bereaved groups: one group who did not receive a letter of condolence and a group that received a letter of condolence 15 days after the death.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •death of a relative patient in intensive care whose relatives were interviewed at least once by resuscitation team
  • •death of an adult relative patient
  • •ICU stay of the relative patient more than 2 days

Exclusion Criteria

  • •death of a pregnant woman
  • •opposition to the use of its data by the patient
  • •relative does not speak French
  • •refusal of the relative

Arms & Interventions

Letter of condolence

Experimental

Letter of condolence 15 days after the death of the relative.

Intervention: Letter of condolence (Other)

No letter of condolence

No Intervention

No letter of condolence

Outcomes

Primary Outcomes

HADS (Hospital Anxiety and Depression Scale)

Time Frame: 1 month

Secondary Outcomes

  • Caesar scale(1 month)
  • IES-R (Impact of Event Scale, Revised)(6 months)
  • ICG (Inventory of Complicated grief)(6 months)
  • HADS (Hospital Anxiety and Depression Scale)(6 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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