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Evaluating the efficacy of an integrated smoking cessation intervention for mental health patients: study protocol for a randomised controlled trial

BACKGROUND: Smoking rates, and associated negative health outcomes, are disproportionately high among people with mental illness compared to the general population. Smoke-free policies within mental health hospitals can positively impact on patients’ motivation and self-efficacy to address their smo...

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Autores principales: Metse, Alexandra P, Bowman, Jenny A, Wye, Paula, Stockings, Emily, Adams, Maree, Clancy, Richard, Terry, Margarett, Wolfenden, Luke, Freund, Megan, Allan, John, Prochaska, Judith J, Wiggers, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091653/
https://www.ncbi.nlm.nih.gov/pubmed/24996596
http://dx.doi.org/10.1186/1745-6215-15-266
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author Metse, Alexandra P
Bowman, Jenny A
Wye, Paula
Stockings, Emily
Adams, Maree
Clancy, Richard
Terry, Margarett
Wolfenden, Luke
Freund, Megan
Allan, John
Prochaska, Judith J
Wiggers, John
author_facet Metse, Alexandra P
Bowman, Jenny A
Wye, Paula
Stockings, Emily
Adams, Maree
Clancy, Richard
Terry, Margarett
Wolfenden, Luke
Freund, Megan
Allan, John
Prochaska, Judith J
Wiggers, John
author_sort Metse, Alexandra P
collection PubMed
description BACKGROUND: Smoking rates, and associated negative health outcomes, are disproportionately high among people with mental illness compared to the general population. Smoke-free policies within mental health hospitals can positively impact on patients’ motivation and self-efficacy to address their smoking. However, without post-discharge support, preadmission smoking behaviours typically resume. This protocol describes a randomised controlled trial that aims to assess the efficacy of linking mental health inpatients to community-based smoking cessation supports upon discharge as a means of reducing smoking prevalence. METHODS/DESIGN: Eight hundred participants with acute mental illness will be recruited into the randomised controlled trial whilst inpatients at one of four psychiatric inpatient facilities in the state of New South Wales, Australia. After completing a baseline interview, participants will be randomly allocated to receive either: ‘Supported Care’, a multimodal smoking cessation intervention; or ‘Normal Care’, consisting of existing hospital care only. The ‘Supported Care’ intervention will consist of a brief motivational interview and a package of self-help material for abstaining from smoking whilst in hospital, and, following discharge, 16 weeks of motivational telephone-based counselling, 12 weeks of free nicotine replacement therapy, and a referral to the Quitline. Data will be collected at 1, 6 and 12 months post-discharge via computer-assisted telephone interview. The primary outcomes are abstinence from smoking (7-day point prevalence and prolonged cessation), and secondary outcomes comprise daily cigarette consumption, nicotine dependence, quit attempts, and readiness to change smoking behaviour. DISCUSSION: If shown to be effective, the study will provide evidence in support of systemic changes in the provision of smoking cessation care to patients following discharge from psychiatric inpatient facilities. TRIAL REGISTRATION: Australian New Zealand Clinical Trials Registry ANZTCN: ACTRN12612001042831. Date registered: 28 September 2012.
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spelling pubmed-40916532014-07-11 Evaluating the efficacy of an integrated smoking cessation intervention for mental health patients: study protocol for a randomised controlled trial Metse, Alexandra P Bowman, Jenny A Wye, Paula Stockings, Emily Adams, Maree Clancy, Richard Terry, Margarett Wolfenden, Luke Freund, Megan Allan, John Prochaska, Judith J Wiggers, John Trials Study Protocol BACKGROUND: Smoking rates, and associated negative health outcomes, are disproportionately high among people with mental illness compared to the general population. Smoke-free policies within mental health hospitals can positively impact on patients’ motivation and self-efficacy to address their smoking. However, without post-discharge support, preadmission smoking behaviours typically resume. This protocol describes a randomised controlled trial that aims to assess the efficacy of linking mental health inpatients to community-based smoking cessation supports upon discharge as a means of reducing smoking prevalence. METHODS/DESIGN: Eight hundred participants with acute mental illness will be recruited into the randomised controlled trial whilst inpatients at one of four psychiatric inpatient facilities in the state of New South Wales, Australia. After completing a baseline interview, participants will be randomly allocated to receive either: ‘Supported Care’, a multimodal smoking cessation intervention; or ‘Normal Care’, consisting of existing hospital care only. The ‘Supported Care’ intervention will consist of a brief motivational interview and a package of self-help material for abstaining from smoking whilst in hospital, and, following discharge, 16 weeks of motivational telephone-based counselling, 12 weeks of free nicotine replacement therapy, and a referral to the Quitline. Data will be collected at 1, 6 and 12 months post-discharge via computer-assisted telephone interview. The primary outcomes are abstinence from smoking (7-day point prevalence and prolonged cessation), and secondary outcomes comprise daily cigarette consumption, nicotine dependence, quit attempts, and readiness to change smoking behaviour. DISCUSSION: If shown to be effective, the study will provide evidence in support of systemic changes in the provision of smoking cessation care to patients following discharge from psychiatric inpatient facilities. TRIAL REGISTRATION: Australian New Zealand Clinical Trials Registry ANZTCN: ACTRN12612001042831. Date registered: 28 September 2012. BioMed Central 2014-07-05 /pmc/articles/PMC4091653/ /pubmed/24996596 http://dx.doi.org/10.1186/1745-6215-15-266 Text en Copyright © 2014 Metse et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Metse, Alexandra P
Bowman, Jenny A
Wye, Paula
Stockings, Emily
Adams, Maree
Clancy, Richard
Terry, Margarett
Wolfenden, Luke
Freund, Megan
Allan, John
Prochaska, Judith J
Wiggers, John
Evaluating the efficacy of an integrated smoking cessation intervention for mental health patients: study protocol for a randomised controlled trial
title Evaluating the efficacy of an integrated smoking cessation intervention for mental health patients: study protocol for a randomised controlled trial
title_full Evaluating the efficacy of an integrated smoking cessation intervention for mental health patients: study protocol for a randomised controlled trial
title_fullStr Evaluating the efficacy of an integrated smoking cessation intervention for mental health patients: study protocol for a randomised controlled trial
title_full_unstemmed Evaluating the efficacy of an integrated smoking cessation intervention for mental health patients: study protocol for a randomised controlled trial
title_short Evaluating the efficacy of an integrated smoking cessation intervention for mental health patients: study protocol for a randomised controlled trial
title_sort evaluating the efficacy of an integrated smoking cessation intervention for mental health patients: study protocol for a randomised controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091653/
https://www.ncbi.nlm.nih.gov/pubmed/24996596
http://dx.doi.org/10.1186/1745-6215-15-266
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