Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/11059
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dc.contributor.authorTaskila, Tainaen_UK
dc.contributor.authorMacAskill, Susanen_UK
dc.contributor.authorColeman, Timen_UK
dc.contributor.authorEtter, Jean-Francoisen_UK
dc.contributor.authorPatel, Mahendraen_UK
dc.contributor.authorClarke, Sarahen_UK
dc.contributor.authorBridson, Rachelen_UK
dc.contributor.authorAveyard, Paulen_UK
dc.date.accessioned2014-02-22T02:59:37Z-
dc.date.available2014-02-22T02:59:37Z-
dc.date.issued2012-03-12en_UK
dc.identifier.urihttp://hdl.handle.net/1893/11059-
dc.description.abstractBackground: Public policy and clinical treatment in tobacco addiction in the UK has focused on cessation: an abrupt attempt to stop all cigarettes. However, recent evidence suggests that allowing more gradual withdrawal from tobacco or even permanent partial substitution by nicotine replacement therapy (NRT) could lead to net benefits to public health. No jurisdiction has introduced smoking reduction programmes in normal clinical care and the best methods for their implementation is uncertain. Community pharmacists offering smoking cessation services in the UK are ideally placed to implement reduction programmes. This pilot study aims therefore to examine the feasibility of implementing smoking reduction programme in pharmacies, and also to see if behavioural support and a longer treatment affect the success rate for cessation. Design and methods: This is a 2 × 2 randomised factorial trial of behavioural support versus no support and short versus standard length reduction programme. The pharmacists will recruit 16 patients per pharmacy, 160 smokers altogether. Pharmacists will randomise each participant by sealed envelopes. In a standard supported programme, the pharmacist will give support for 34 weeks, inviting participants to set a treatment goal and providing advice on how to reduce cigarette use. Participants in the short programme will be given the same advice on how to reduce but will reduce smoking over four weeks. Participants in the no support arms will be given a leaflet that describes the reduction programmes in 4-week and 34-week format. All participants are encouraged to use of NRT to support the reduction. These processes will be measured by recording the number of recruited smokers; percentage of those who reduce and sustain their consumption to at least 50% of baseline value, and the proportion of people who attain 4 weeks abstinence and 6 months abstinence. Interviews will assess smokers' and pharmacists' views on the way the programme ran. Discussion: This is a pilot study to assess the feasibility of offering smoking reduction programme within pharmacies that offer naturalistic setting to show population benefit from these programmes. Findings from this trial will inform the development of evidence-based treatment for smokers who want to reduce and best approaches to engage reluctant quitters onto the programme. Trial Registration: Current Controlled Trials ISRCTN 2010-019259-24en_UK
dc.language.isoenen_UK
dc.publisherBioMed Central Ltden_UK
dc.relationTaskila T, MacAskill S, Coleman T, Etter J, Patel M, Clarke S, Bridson R & Aveyard P (2012) A Randomised trial of nicotine assisted reduction to stop in pharmacies - The RedPharm Study. BMC Public Health, 12 (182). https://doi.org/10.1186/1471-2458-12-182en_UK
dc.rights© 2012 Taskila et al; licensee BioMed Central Ltd. 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.en_UK
dc.rights.urihttp://creativecommons.org/licenses/by/2.0/en_UK
dc.subjectSmokingen_UK
dc.subjectTobacco Dependenceen_UK
dc.subjectControlled Clinical Trialsen_UK
dc.subjectRandomizeden_UK
dc.subjectPharmacistsen_UK
dc.subjectHarm Reductionen_UK
dc.titleA Randomised trial of nicotine assisted reduction to stop in pharmacies - The RedPharm Studyen_UK
dc.typeJournal Articleen_UK
dc.identifier.doi10.1186/1471-2458-12-182en_UK
dc.citation.jtitleBMC Public Healthen_UK
dc.citation.issn1471-2458en_UK
dc.citation.volume12en_UK
dc.citation.issue182en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.author.emailsusan.macaskill@stir.ac.uken_UK
dc.contributor.affiliationUniversity of Birminghamen_UK
dc.contributor.affiliationInstitute for Social Marketingen_UK
dc.contributor.affiliationUniversity of Nottinghamen_UK
dc.contributor.affiliationUniversity of Genevaen_UK
dc.contributor.affiliationUniversity of Huddersfielden_UK
dc.contributor.affiliationUniversity of Birminghamen_UK
dc.contributor.affiliationUniversity of Birminghamen_UK
dc.contributor.affiliationUniversity of Birminghamen_UK
dc.identifier.isiWOS:000304863500001en_UK
dc.identifier.scopusid2-s2.0-84857970601en_UK
dc.identifier.wtid733583en_UK
dcterms.dateAccepted2012-03-12en_UK
dc.date.filedepositdate2013-02-22en_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorTaskila, Taina|en_UK
local.rioxx.authorMacAskill, Susan|en_UK
local.rioxx.authorColeman, Tim|en_UK
local.rioxx.authorEtter, Jean-Francois|en_UK
local.rioxx.authorPatel, Mahendra|en_UK
local.rioxx.authorClarke, Sarah|en_UK
local.rioxx.authorBridson, Rachel|en_UK
local.rioxx.authorAveyard, Paul|en_UK
local.rioxx.projectInternal Project|University of Stirling|https://isni.org/isni/0000000122484331en_UK
local.rioxx.freetoreaddate2013-02-22en_UK
local.rioxx.licencehttp://creativecommons.org/licenses/by/2.0/|2013-02-22|en_UK
local.rioxx.filenameTaskila Macaskill redpharm1471-2458-12-182.pdfen_UK
local.rioxx.filecount1en_UK
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