Smoking cessation using preference-based tools among socially disadvantaged smokers: study protocol for a pragmatic, multicentre randomised controlled trial

被引:5
作者
El-Khoury, Fabienne [1 ,2 ]
El Aarbaoui, Tarik [1 ]
Heron, Megane [1 ]
Hejblum, Gilles [3 ]
Metadieu, Brigitte [4 ]
Le Faou, Anne-Laurence [5 ,6 ]
Ibanez, Gladys [7 ,8 ]
Melchior, Maria [1 ]
机构
[1] Sorbonne Univ, Inst Pierre Louis Epidemiol & Sante Publ IPLESP, Dept Social Epidemiol, INSERM,UMR S 1136, Paris, France
[2] GHU PARIS Psychiatr Neurosci, Dept Epidemiol, Paris, France
[3] Sorbonne Univ, Inst Pierre Louis Epidemiol & Sante Publ IPLESP, CLEPIVIR Res Team, INSERM,UMR S 1136, Paris, France
[4] CSAPA Charonne, Paris, France
[5] Hop Univ Paris Ouest, Hop Europeen Georges Pompidou, Addict Ctr, Pole Psychiat Addictol, Paris, France
[6] Federat Hosp Univ, Network Res Subst Use Disorder, Paris, France
[7] Sorbonne Univ, Inst Pierre Louis Epidemiol & Sante Publ IPLESP, INSERM, Fac Med, Paris, France
[8] SFTG Rech Soc Format Therapeut Generaliste Rech, Paris, France
关键词
preventive medicine; primary care; public health; VALIDITY;
D O I
10.1136/bmjopen-2021-048859
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Many smoking cessation aids such as nicotine replacement treatments and e-cigarettes have been proven effective in aiding smoking cessation attempts. Encouraging smokers with low socioeconomic position (SEP) to choose their smoking aid tool based on their preferences, and giving that tool free of charge, might increase the odds of smoking cessation. This trial examines the effectiveness of the 'STOP' (Sevrage Tabagique a l'aide d'Outils dedies selon la Preference: Smoking cessation using preference-based tools), a preference-based smoking cessation intervention for smokers with low SEP. Methods and analysis The STOP study is a randomised, multicentre, controlled trial (RCT). Smokers with low SEP and wishing to quit will be randomised to either the intervention or the control group (standard care). Participants in the intervention group will be asked to choose between different types of nicotine substitutes (patches, inhalers, gum, tablets, etc) and/or an electronic cigarette which will be delivered free of charge to aid their smoking cessation attempt. The primary outcome will be smoking abstinence at 6 months after inclusion, defined as self-reported 7-day point prevalence of tobacco abstinence. Secondary outcomes include the total number of days of abstinence at 6 months after inclusion, 7-day point prevalence tobacco abstinence at 1 and 3 months after inclusion and number of relapses. The study will also include an economic evaluation, and a process evaluation using a mixed methods approach. Ethics and dissemination The study was approved by the 'ile de France II' Institutional Review Board on 8 September 2020 (CPP ile de France II; Ref No: 20.01.31.65528 RIPH2 HPS), and results will be published in a peer-reviewed journal.
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收藏
页数:9
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