Evaluating the effectiveness and cost-effectiveness of the Smoking Treatment Optimisation in Pharmacies (STOP) intervention: protocol for a cluster randomised controlled trial

被引:3
|
作者
Sohanpal, Ratna [1 ]
Jumbe, Sandra [1 ]
James, Wai-Yee [1 ]
Steed, Liz [1 ]
Yau, Tammy [2 ]
Rivas, Carol [3 ]
Madurasinghe, Vichithranie [1 ]
Houlihan, Colin [1 ]
Berdunisov, Vlad [1 ]
Taylor, Matthew [4 ]
Taylor, Stephanie J. C. [1 ]
Griffiths, Chris [1 ]
Eldridge, Sandra [1 ]
Walton, Robert [1 ]
机构
[1] Queen Mary Univ London, Barts & London Sch Med & Dent, Blizard Inst, Ctr Primary Care & Publ Hlth, London, England
[2] Calif Northstate Univ, 9700 West Taron Dr, Elk Grove, CA 95757 USA
[3] UCL, Inst Educ, London, England
[4] Univ York, York Hlth Econ Consortium, York, N Yorkshire, England
关键词
Smoking cessation; Community pharmacy; Recruitment; Retention; Behaviour change; Cluster randomised controlled trial; Quit rate;
D O I
10.1186/s13063-019-3368-6
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
BackgroundNHS community pharmacies provide effective smoking cessation services; however, there is scope for increasing throughput and improving quit rates. This trial examines whether the Smoking Treatment Optimisation in Pharmacies (STOP) intervention can improve smoker engagement to increase service throughput, retention and quitting.MethodsThis study is a pragmatic, cluster randomised controlled trial in 60 pharmacies in England and Wales. All workers in intervention pharmacies are offered STOP training while control pharmacies provide usual care. The STOP intervention, based on behavioural and organisational theories, comprises educational sessions for staff and environmental prompts in the pharmacy. Intervention fidelity is assessed by actors visiting pharmacies posing as smokers. The primary outcome is throughput, defined as the number of smokers who join the programme, set a firm quit date and undergo at least one stop smoking treatment session, and is measured using routinely collected data. Secondary outcomes include retention and quit rates at 4 weeks and continuous abstinence at 6 months verified by salivary cotinine. Cost-effectiveness is estimated using quality-adjusted life years and the probability that the intervention is effective at different levels of willingness to pay is calculated.DiscussionThe trial will generate evidence to inform the public health smoking cessation strategy in England and Wales, and may help to shape service commissioning decisions. The STOP intervention model may help inform the undertaking of a range of health behaviour change tasks in community pharmacies.Trial registrationClinicalTrials.gov, ISRCTN16351033. Retrospectively registered on 21 March 2017.
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页数:12
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