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Impact of the condolence letter on the experience of bereaved families after a death in intensive care: study protocol for a randomized controlled trial
BACKGROUND: As intensive care mortality is high, end of life is a subject of major concern for intensivists. In this context, relatives are particularly vulnerable and prone to post-ICU syndrome, in the form of high levels of anxiety, depression, post-traumatic stress, and complicated grief. Grievin...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4761130/ https://www.ncbi.nlm.nih.gov/pubmed/26897630 http://dx.doi.org/10.1186/s13063-016-1212-9 |
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author | Kentish-Barnes, Nancy Chevret, Sylvie Azoulay, Elie |
author_facet | Kentish-Barnes, Nancy Chevret, Sylvie Azoulay, Elie |
author_sort | Kentish-Barnes, Nancy |
collection | PubMed |
description | BACKGROUND: As intensive care mortality is high, end of life is a subject of major concern for intensivists. In this context, relatives are particularly vulnerable and prone to post-ICU syndrome, in the form of high levels of anxiety, depression, post-traumatic stress, and complicated grief. Grieving families suffer from a feeling of abandonment and evoke the need to get back in touch with the team to ask questions and remove doubts, but very few actually do. Aiding families during the grieving process is an important aspect of palliative care. A condolence letter represents an opportunity to recognize the pain of the family member and the strong tie that linked the family member to the ICU team, and to offer additional information if necessary. The goal of the study is to measure the impact of the condolence letter on the experience of bereaved families after a death in the ICU. Our hypothesis is that a post-death follow-up in the form of a condolence letter sent by the ICU physician who was in charge of the patient may help to reduce the risks of presenting symptoms of anxiety/depression, post-traumatic stress, and complicated grief. METHODS/DESIGN: This is a randomized, controlled, multicenter study. Research will compare two groups of bereaved family members: one group that does not receive a condolence letter (control) and one group that receives a condolence letter 15 days after the death (intervention). Each of the 22 participating centers will include 12 relatives. Participating relatives will be followed up by phone with a call at 1 month and one at 6 months to complete questionnaires, permitting evaluation of post-ICU burden. The main outcome is anxiety and depression measured at 1 month. Other outcomes include evaluation of quality of dying and death, post-traumatic stress, and complicated grief. DISCUSSION: This study will allow us to assess if sending a condolence letter can reduce the risks of presenting symptoms of anxiety and depression, complicated grief, and symptoms of post-traumatic stress disorder after the death of a loved one in the ICU. TRIAL REGISTRATION: Clinical Trials registration number: Clinicaltrials.gov NCT02325297 (23 December 2014). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-016-1212-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4761130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47611302016-02-21 Impact of the condolence letter on the experience of bereaved families after a death in intensive care: study protocol for a randomized controlled trial Kentish-Barnes, Nancy Chevret, Sylvie Azoulay, Elie Trials Study Protocol BACKGROUND: As intensive care mortality is high, end of life is a subject of major concern for intensivists. In this context, relatives are particularly vulnerable and prone to post-ICU syndrome, in the form of high levels of anxiety, depression, post-traumatic stress, and complicated grief. Grieving families suffer from a feeling of abandonment and evoke the need to get back in touch with the team to ask questions and remove doubts, but very few actually do. Aiding families during the grieving process is an important aspect of palliative care. A condolence letter represents an opportunity to recognize the pain of the family member and the strong tie that linked the family member to the ICU team, and to offer additional information if necessary. The goal of the study is to measure the impact of the condolence letter on the experience of bereaved families after a death in the ICU. Our hypothesis is that a post-death follow-up in the form of a condolence letter sent by the ICU physician who was in charge of the patient may help to reduce the risks of presenting symptoms of anxiety/depression, post-traumatic stress, and complicated grief. METHODS/DESIGN: This is a randomized, controlled, multicenter study. Research will compare two groups of bereaved family members: one group that does not receive a condolence letter (control) and one group that receives a condolence letter 15 days after the death (intervention). Each of the 22 participating centers will include 12 relatives. Participating relatives will be followed up by phone with a call at 1 month and one at 6 months to complete questionnaires, permitting evaluation of post-ICU burden. The main outcome is anxiety and depression measured at 1 month. Other outcomes include evaluation of quality of dying and death, post-traumatic stress, and complicated grief. DISCUSSION: This study will allow us to assess if sending a condolence letter can reduce the risks of presenting symptoms of anxiety and depression, complicated grief, and symptoms of post-traumatic stress disorder after the death of a loved one in the ICU. TRIAL REGISTRATION: Clinical Trials registration number: Clinicaltrials.gov NCT02325297 (23 December 2014). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-016-1212-9) contains supplementary material, which is available to authorized users. BioMed Central 2016-02-20 /pmc/articles/PMC4761130/ /pubmed/26897630 http://dx.doi.org/10.1186/s13063-016-1212-9 Text en © Kentish-Barnes et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Study Protocol Kentish-Barnes, Nancy Chevret, Sylvie Azoulay, Elie Impact of the condolence letter on the experience of bereaved families after a death in intensive care: study protocol for a randomized controlled trial |
title | Impact of the condolence letter on the experience of bereaved families after a death in intensive care: study protocol for a randomized controlled trial |
title_full | Impact of the condolence letter on the experience of bereaved families after a death in intensive care: study protocol for a randomized controlled trial |
title_fullStr | Impact of the condolence letter on the experience of bereaved families after a death in intensive care: study protocol for a randomized controlled trial |
title_full_unstemmed | Impact of the condolence letter on the experience of bereaved families after a death in intensive care: study protocol for a randomized controlled trial |
title_short | Impact of the condolence letter on the experience of bereaved families after a death in intensive care: study protocol for a randomized controlled trial |
title_sort | impact of the condolence letter on the experience of bereaved families after a death in intensive care: study protocol for a randomized controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4761130/ https://www.ncbi.nlm.nih.gov/pubmed/26897630 http://dx.doi.org/10.1186/s13063-016-1212-9 |
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