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Advance care planning in patients with incurable cancer: study protocol for a randomised controlled trial
INTRODUCTION: There is limited evidence documenting the effectiveness of Advance Care Planning (ACP) in cancer care. The present randomised trial is designed to evaluate whether the administration of formal ACP improves compliance with patients' end-of-life (EOL) wishes and patient and family s...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5168675/ https://www.ncbi.nlm.nih.gov/pubmed/27909034 http://dx.doi.org/10.1136/bmjopen-2016-012387 |
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author | Johnson, Stephanie Clayton, Josephine Butow, Phyllis N Silvester, William Detering, Karen Hall, Jane Kiely, Belinda E Cebon, Jonathon Clarke, Stephen Bell, Melanie L Stockler, Martin Beale, Phillip Tattersall, Martin H N |
author_facet | Johnson, Stephanie Clayton, Josephine Butow, Phyllis N Silvester, William Detering, Karen Hall, Jane Kiely, Belinda E Cebon, Jonathon Clarke, Stephen Bell, Melanie L Stockler, Martin Beale, Phillip Tattersall, Martin H N |
author_sort | Johnson, Stephanie |
collection | PubMed |
description | INTRODUCTION: There is limited evidence documenting the effectiveness of Advance Care Planning (ACP) in cancer care. The present randomised trial is designed to evaluate whether the administration of formal ACP improves compliance with patients' end-of-life (EOL) wishes and patient and family satisfaction with care. METHODS AND ANALYSIS: A randomised control trial in eight oncology centres across New South Wales and Victoria, Australia, is designed to assess the efficacy of a formal ACP intervention for patients with cancer. Patients with incurable cancer and an expected survival of 3–12 months, plus a nominated family member or friend will be randomised to receive either standard care or standard care plus a formal ACP intervention. The project sample size is 210 patient–family/friend dyads. The primary outcome measure is family/friend-reported: (1) discussion with the patient about their EOL wishes and (2) perception that the patient's EOL wishes were met. Secondary outcome measures include: documentation of and compliance with patient preferences for medical intervention at the EOL; the family/friend's perception of the quality of the patient's EOL care; the impact of death on surviving family; patient–family and patient–healthcare provider communication about EOL care; patient and family/friend satisfaction with care; quality of life of patient and family/friend subsequent to trial entry, the patient's strength of preferences for quality of life and length of life; the costs of care subsequent to trial entry and place of death. ETHICS AND DISSEMINATION: Ethical approval was received from the Sydney Local Health District (RPA Zone) Human Research Ethical Committee, Australia (Protocol number X13-0064). Study results will be submitted for publication in peer-reviewed journals and presented at national and international conferences. TRIAL REGISTRATION NUMBER: Pre-results; ACTRN12613001288718. |
format | Online Article Text |
id | pubmed-5168675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51686752017-01-10 Advance care planning in patients with incurable cancer: study protocol for a randomised controlled trial Johnson, Stephanie Clayton, Josephine Butow, Phyllis N Silvester, William Detering, Karen Hall, Jane Kiely, Belinda E Cebon, Jonathon Clarke, Stephen Bell, Melanie L Stockler, Martin Beale, Phillip Tattersall, Martin H N BMJ Open Oncology INTRODUCTION: There is limited evidence documenting the effectiveness of Advance Care Planning (ACP) in cancer care. The present randomised trial is designed to evaluate whether the administration of formal ACP improves compliance with patients' end-of-life (EOL) wishes and patient and family satisfaction with care. METHODS AND ANALYSIS: A randomised control trial in eight oncology centres across New South Wales and Victoria, Australia, is designed to assess the efficacy of a formal ACP intervention for patients with cancer. Patients with incurable cancer and an expected survival of 3–12 months, plus a nominated family member or friend will be randomised to receive either standard care or standard care plus a formal ACP intervention. The project sample size is 210 patient–family/friend dyads. The primary outcome measure is family/friend-reported: (1) discussion with the patient about their EOL wishes and (2) perception that the patient's EOL wishes were met. Secondary outcome measures include: documentation of and compliance with patient preferences for medical intervention at the EOL; the family/friend's perception of the quality of the patient's EOL care; the impact of death on surviving family; patient–family and patient–healthcare provider communication about EOL care; patient and family/friend satisfaction with care; quality of life of patient and family/friend subsequent to trial entry, the patient's strength of preferences for quality of life and length of life; the costs of care subsequent to trial entry and place of death. ETHICS AND DISSEMINATION: Ethical approval was received from the Sydney Local Health District (RPA Zone) Human Research Ethical Committee, Australia (Protocol number X13-0064). Study results will be submitted for publication in peer-reviewed journals and presented at national and international conferences. TRIAL REGISTRATION NUMBER: Pre-results; ACTRN12613001288718. BMJ Publishing Group 2016-12-01 /pmc/articles/PMC5168675/ /pubmed/27909034 http://dx.doi.org/10.1136/bmjopen-2016-012387 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Oncology Johnson, Stephanie Clayton, Josephine Butow, Phyllis N Silvester, William Detering, Karen Hall, Jane Kiely, Belinda E Cebon, Jonathon Clarke, Stephen Bell, Melanie L Stockler, Martin Beale, Phillip Tattersall, Martin H N Advance care planning in patients with incurable cancer: study protocol for a randomised controlled trial |
title | Advance care planning in patients with incurable cancer: study protocol for a randomised controlled trial |
title_full | Advance care planning in patients with incurable cancer: study protocol for a randomised controlled trial |
title_fullStr | Advance care planning in patients with incurable cancer: study protocol for a randomised controlled trial |
title_full_unstemmed | Advance care planning in patients with incurable cancer: study protocol for a randomised controlled trial |
title_short | Advance care planning in patients with incurable cancer: study protocol for a randomised controlled trial |
title_sort | advance care planning in patients with incurable cancer: study protocol for a randomised controlled trial |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5168675/ https://www.ncbi.nlm.nih.gov/pubmed/27909034 http://dx.doi.org/10.1136/bmjopen-2016-012387 |
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