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Study protocol: A cluster randomised controlled trial of implementation intentions to reduce smoking initiation in adolescents

BACKGROUND: The current literature suggests that forming implementation intentions (simple ‘if-then’ plans) about how to refuse the offer of a cigarette may be an effective intervention to reduce smoking initiation in adolescents. This study is a pragmatic trial to test the effectiveness and cost-ef...

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Autores principales: Conner, Mark, Grogan, Sarah, Lawton, Rebecca, Armitage, Christopher, West, Robert, Siddiqi, Kamran, Gannon, Brenda, Torgerson, Carole, Flett, Keira, Simms-Ellis, Ruth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3623649/
https://www.ncbi.nlm.nih.gov/pubmed/23332020
http://dx.doi.org/10.1186/1471-2458-13-54
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author Conner, Mark
Grogan, Sarah
Lawton, Rebecca
Armitage, Christopher
West, Robert
Siddiqi, Kamran
Gannon, Brenda
Torgerson, Carole
Flett, Keira
Simms-Ellis, Ruth
author_facet Conner, Mark
Grogan, Sarah
Lawton, Rebecca
Armitage, Christopher
West, Robert
Siddiqi, Kamran
Gannon, Brenda
Torgerson, Carole
Flett, Keira
Simms-Ellis, Ruth
author_sort Conner, Mark
collection PubMed
description BACKGROUND: The current literature suggests that forming implementation intentions (simple ‘if-then’ plans) about how to refuse the offer of a cigarette may be an effective intervention to reduce smoking initiation in adolescents. This study is a pragmatic trial to test the effectiveness and cost-effectiveness of such an intervention in reducing smoking initiation in a sample of UK adolescents. METHODS/DESIGN: A cluster randomised controlled trial with at least 36 schools randomised to receive an implementation intention intervention targeting reducing smoking initiation (intervention group) or increasing homework (control group). Interventions will be conducted at the classroom level and be repeated every six months for four years (eight interventions). Objectively assessed (carbon monoxide monitor) and self-reported smoking plus smoking related cognitions (e.g., smoking intentions, attitudes, norms and self-efficacy) will be assessed at baseline and 12, 24, 36 and 48 months post baseline. Objectively assessed smoking at 48 months post baseline will be the primary outcome variable. Health economic analyses will assess life years gained. DISCUSSION: The results of the trial will provide information on the impact of a repeated implementation intention for refusing offers of cigarettes on rates of smoking initiation in adolescents. TRIAL REGISTRATION: ISRCTN27596806
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spelling pubmed-36236492013-04-12 Study protocol: A cluster randomised controlled trial of implementation intentions to reduce smoking initiation in adolescents Conner, Mark Grogan, Sarah Lawton, Rebecca Armitage, Christopher West, Robert Siddiqi, Kamran Gannon, Brenda Torgerson, Carole Flett, Keira Simms-Ellis, Ruth BMC Public Health Study Protocol BACKGROUND: The current literature suggests that forming implementation intentions (simple ‘if-then’ plans) about how to refuse the offer of a cigarette may be an effective intervention to reduce smoking initiation in adolescents. This study is a pragmatic trial to test the effectiveness and cost-effectiveness of such an intervention in reducing smoking initiation in a sample of UK adolescents. METHODS/DESIGN: A cluster randomised controlled trial with at least 36 schools randomised to receive an implementation intention intervention targeting reducing smoking initiation (intervention group) or increasing homework (control group). Interventions will be conducted at the classroom level and be repeated every six months for four years (eight interventions). Objectively assessed (carbon monoxide monitor) and self-reported smoking plus smoking related cognitions (e.g., smoking intentions, attitudes, norms and self-efficacy) will be assessed at baseline and 12, 24, 36 and 48 months post baseline. Objectively assessed smoking at 48 months post baseline will be the primary outcome variable. Health economic analyses will assess life years gained. DISCUSSION: The results of the trial will provide information on the impact of a repeated implementation intention for refusing offers of cigarettes on rates of smoking initiation in adolescents. TRIAL REGISTRATION: ISRCTN27596806 BioMed Central 2013-01-19 /pmc/articles/PMC3623649/ /pubmed/23332020 http://dx.doi.org/10.1186/1471-2458-13-54 Text en Copyright © 2013 Conner et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Study Protocol
Conner, Mark
Grogan, Sarah
Lawton, Rebecca
Armitage, Christopher
West, Robert
Siddiqi, Kamran
Gannon, Brenda
Torgerson, Carole
Flett, Keira
Simms-Ellis, Ruth
Study protocol: A cluster randomised controlled trial of implementation intentions to reduce smoking initiation in adolescents
title Study protocol: A cluster randomised controlled trial of implementation intentions to reduce smoking initiation in adolescents
title_full Study protocol: A cluster randomised controlled trial of implementation intentions to reduce smoking initiation in adolescents
title_fullStr Study protocol: A cluster randomised controlled trial of implementation intentions to reduce smoking initiation in adolescents
title_full_unstemmed Study protocol: A cluster randomised controlled trial of implementation intentions to reduce smoking initiation in adolescents
title_short Study protocol: A cluster randomised controlled trial of implementation intentions to reduce smoking initiation in adolescents
title_sort study protocol: a cluster randomised controlled trial of implementation intentions to reduce smoking initiation in adolescents
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3623649/
https://www.ncbi.nlm.nih.gov/pubmed/23332020
http://dx.doi.org/10.1186/1471-2458-13-54
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