"Impacts of the Letter of Condolence to the Bereaved Families Experience After a Death in ICU " - Study Famirea 22
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
Letter of condolence 15 days after the death of the relative.
Intervention: Letter of condolence (Other)
No letter of condolence
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)
