The introduction of the intervention may help to reduce the risks of presenting symptoms of complicated grief, depression, anxiety. Furthermore, it may improve the quality of experiences with bereavement care in the ICU.
ID
Bron
Verkorte titel
Aandoening
Not specified, target group: relatives of patients who died in the ICU
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Complicated grief measured with the 'Traumatic Grief Inventory-Self Report Version', 19 items.
Achtergrond van het onderzoek
When a patient dies at the ICU, most of the relatives in the intensive care unit (ICU) need to make a rapid transition from aiming at recovery of their beloved one, to preparation for an unavoidable death. Bereaved relatives may develop complicated grief as a consequence of this burdensome situation. Complicated grief has been included in the Post Intensive Care Syndrome Family (PICS-F) and is characterized by intense symptoms of grief enduring for more than 6 months post-loss, separation distress, intrusive thoughts, and feelings of emptiness or meaninglessness. It could lead to negative health outcomes, advanced medical service utilization, and high economic costs. However, little is known on the true prevalence of complicated grief in bereaved relatives in the ICU.
Patients in Dutch hospitals die rapidly, resulting in a dignified death with a low burden of suffering and little signs of discomfort. It is therefore valuable to assess complicated grief and the experiences with quality of bereavement care in relatives in a Dutch ICU. This study aims to contribute in knowledge on complicated grief.
Doel van het onderzoek
The introduction of the intervention may help to reduce the risks of presenting symptoms of complicated grief, depression, anxiety. Furthermore, it may improve the quality of experiences with bereavement care in the ICU.
Onderzoeksopzet
Cohort 1, Patient died in 2018
Cohort 2, Patient died in 2019
Onderzoeksproduct en/of interventie
Introduction of newly developed bundle of interventions in bereavement care, including an information leaflet on loss and grief, a condolence greeting card, material to make a memory, and follow-up call by nurses 6 weeks post-death.
Publiek
Wetenschappelijk
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Bereaved relatives after the death of an adult patient in the ICU, fulfilling all inclusion criteria:
- Death of an adult (age>18) patient
- Death of a patient whose relative has met the ICU team at at least once before the death
- Relative has understanding of the Dutch language
- Relatives are considered legally capable
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- Refusal of the relative
- Unknown contact details
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiënten Data (IPD)
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
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Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL7875 |
Ander register | Medical Ethics Committee Erasmus MC : MEC-2018-1598 |