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A randomised trial of nicotine assisted reduction to stop in pharmacies - the redpharm study

机译:尼古丁辅助减量停止药房的随机试验-Redpharm研究

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Background 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 2010-019259-24
机译:背景技术在英国,吸烟成瘾的公共政策和临床治疗都集中在戒烟上:突然尝试停止所有卷烟。但是,最近的证据表明,允许逐步从烟草中戒烟,甚至通过尼古丁替代疗法(NRT)进行永久性部分替代,可能会为公共卫生带来净收益。没有辖区在正常的临床护理中引入减少吸烟的计划,实施这些计划的最佳方法尚不确定。在英国提供戒烟服务的社区药剂师非常适合实施减少吸烟计划。因此,该初步研究旨在检查在药房实施减少吸烟计划的可行性,并查看行为支持和更长的治疗是否会影响戒烟的成功率。设计和方法这是一项2×2的关于行为支持与无支持以及短期与标准长度减少计划的随机析因试验。每个药房的药剂师将招募16名患者,总共160名吸烟者。药剂师将通过密封的信封将每个参与者随机分组。在一个标准的支持计划中,该药剂师将提供34周的支持,邀请参与者制定治疗目标并提供有关减少香烟使用量的建议。短期计划的参与者将获得关于如何减少吸烟的相同建议,但将在四个星期内减少吸烟。不支持小组的参与者将获得一份传单,以4周和34周的形式描述减少计划。鼓励所有参与者使用NRT来支持减少量。这些过程将通过记录吸烟者的人数来衡量;减少和维持其消费量至少达到基准值的50%的人所占的百分比,以及禁食4周和禁食6个月的人所占的比例。访谈将评估吸烟者和药剂师对该计划的运行方式的看法。讨论这是一项试点研究,旨在评估在提供自然环境以显示人口从这些计划中受益的药房内提供减少吸烟计划的可行性。该试验的结果将为希望减少吸烟者的循证治疗方法的发展以及将不情愿的戒烟者纳入该计划的最佳方法提供信息。试用注册当前对照试验ISRCTN 2010-019259-24

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