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新西兰基于社区的三臂实用随机对照试验研究尼古丁盐电子烟、烟碱及二者联合戒烟效果的方案

Effectiveness of nicotine salt vapes, cytisine, and a combination of these products, for smoking cessation in New Zealand: protocol for a three-arm, pragmatic, community-based randomised controlled trial.

机构信息

School of Population Health, National Institute for Health Innovation, The University of Auckland, Private Bag 92019, Auckland, 1142, New Zealand.

School of Pharmacy, The University of Auckland, Private Bag 92019, Auckland, 1142, New Zealand.

出版信息

BMC Public Health. 2023 Sep 11;23(1):1760. doi: 10.1186/s12889-023-16665-w.

Abstract

BACKGROUND

Combining short-acting nicotine replacement therapy with varenicline increases smoking cessation rates compared with varenicline alone, but not all people tolerate these medications or find them helpful. We aim to investigate the therapeutic potential of an analogous combination, by evaluating the effectiveness, safety, and acceptability of combining nicotine salt e-cigarettes with cytisine, compared to nicotine salt e-cigarettes or cytisine only, on smoking abstinence at six months.

METHODS

A pragmatic, community-based, investigator-blinded, randomised superiority trial design will be utilised. Eligible participants will be people who smoke daily (N = 800, 90% power) from throughout New Zealand, who are: aged ≥ 18 years, motivated to quit in the next two weeks, able to provide online consent, willing to use e-cigarettes and/or cytisine, and have daily access to a mobile phone. Recruitment will utilise multi-media advertising. Participants will be randomised (3:3:2 ratio) to 12 weeks of: 1) e-cigarettes (closed pod system, 3% nicotine salt, tobacco flavour) plus cytisine; 2) e-cigarettes alone, or 3) cytisine alone. All groups will receive a six-month, text-message-based behavioural support programme. The primary outcome is self-reported, biochemically verified, continuous abstinence at six months post-quit date. Secondary outcomes, measured at quit date, then one, three, six, and 12 months post-quit date, include self-reported continuous abstinence, 7-day point prevalence abstinence, cigarettes smoked per day, withdrawal and urge to smoke, time to (re)lapse, treatment use and compliance, treatment crossover, dual-use, use of other cessation products, change in e-cigarette products, continuation of product use, acceptability, change in health state, health-related quality of life, change in body mass index, adverse events, and cost per quitter.

DISCUSSION

Pragmatic trials are of particular value as they reflect the 'real world' impact of interventions. The trial will provide some of the first evidence on the effectiveness of combining nicotine salt e-cigarettes with cytisine for smoking cessation, in a country with strong tobacco control policy. Findings will be incorporated into relevant systematic reviews, informing practice and policy.

TRIAL REGISTRATION

NCT05311085 ClinicalTrials.gov. Registered 5th April, 2022.

摘要

背景

与单独使用伐伦克林相比,将短效尼古丁替代疗法与伐尼克兰联合使用可提高戒烟率,但并非所有人都能耐受这些药物或发现它们有帮助。我们旨在通过评估尼古丁盐电子烟与卡替洛尔联合使用在六个月内戒烟的有效性、安全性和可接受性,来研究类似联合治疗的治疗潜力,与尼古丁盐电子烟或卡替洛尔单独使用相比。

方法

将采用实用、基于社区、研究者盲法、随机优势试验设计。符合条件的参与者将是每天吸烟的人(N=800,90%的功效)来自新西兰各地,符合以下条件:年龄≥18 岁,在未来两周内有戒烟意愿,能够在线提供同意,愿意使用电子烟和/或卡替洛尔,并且每天都能使用手机。招募将利用多媒体广告进行。参与者将按 3:3:2 的比例随机分配到 12 周的以下治疗组:1)电子烟(封闭式 pod 系统,3%尼古丁盐,烟草味)加卡替洛尔;2)单独使用电子烟,或 3)单独使用卡替洛尔。所有组都将接受为期六个月的基于短信的行为支持计划。主要结局是自我报告、生物化学验证的连续戒烟率,在戒烟日期后六个月。次要结局,在戒烟日期、然后在戒烟日期后 1、3、6 和 12 个月测量,包括自我报告的连续戒烟、7 天点流行率戒烟、每天吸烟量、戒断和吸烟欲望、(再)复发时间、治疗使用和依从性、治疗交叉、双重使用、其他戒烟产品的使用、电子烟产品的变化、产品继续使用、可接受性、健康状况变化、健康相关生活质量变化、体重指数变化、不良事件和每位戒烟者的成本。

讨论

实用试验具有特别的价值,因为它们反映了干预措施的“现实世界”影响。该试验将提供关于在具有强大烟草控制政策的国家中联合使用尼古丁盐电子烟和卡替洛尔戒烟的有效性的一些首批证据。研究结果将被纳入相关的系统评价,为实践和政策提供信息。

试验注册

NCT05311085 ClinicalTrials.gov。2022 年 4 月 5 日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a01/10494376/78570da94f60/12889_2023_16665_Fig1_HTML.jpg

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