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一项关于即时自适应干预戒烟(Quit Sense)的自动化在线可行性随机对照试验

An Automated, Online Feasibility Randomized Controlled Trial of a Just-In-Time Adaptive Intervention for Smoking Cessation (Quit Sense).

机构信息

Behavioural and Implementation Science Group, School of Health Sciences, University of East Anglia, Norwich, UK.

Addiction Research Group, Norwich Medical School, University of East Anglia, Norwich, UK.

出版信息

Nicotine Tob Res. 2023 Jun 9;25(7):1319-1329. doi: 10.1093/ntr/ntad032.

Abstract

INTRODUCTION

Learned smoking cues from a smoker's environment are a major cause of lapse and relapse. Quit Sense, a theory-guided Just-In-Time Adaptive Intervention smartphone app, aims to help smokers learn about their situational smoking cues and provide in-the-moment support to help manage these when quitting.

METHODS

A two-arm feasibility randomized controlled trial (N = 209) to estimate parameters to inform a definitive evaluation. Smoker's willing to make a quit attempt were recruited using online paid-for adverts and randomized to "usual care" (text message referral to NHS SmokeFree website) or "usual care" plus a text message invitation to install Quit Sense. Procedures, excluding manual follow-up for nonresponders, were automated. Follow-up at 6 weeks and 6 months included feasibility, intervention engagement, smoking-related, and economic outcomes. Abstinence was verified using cotinine assessment from posted saliva samples.

RESULTS

Self-reported smoking outcome completion rates at 6 months were 77% (95% CI 71%, 82%), viable saliva sample return rate was 39% (95% CI 24%, 54%), and health economic data 70% (95% CI 64%, 77%). Among Quit Sense participants, 75% (95% CI 67%, 83%) installed the app and set a quit date and, of those, 51% engaged for more than one week. The 6-month biochemically verified sustained abstinence rate (anticipated primary outcome for definitive trial), was 11.5% (12/104) among Quit Sense participants and 2.9% (3/105) for usual care (adjusted odds ratio = 4.57, 95% CIs 1.23, 16.94). No evidence of between-group differences in hypothesized mechanisms of action was found.

CONCLUSIONS

Evaluation feasibility was demonstrated alongside evidence supporting the effectiveness potential of Quit Sense.

IMPLICATIONS

Running a primarily automated trial to initially evaluate Quit Sense was feasible, resulting in modest recruitment costs and researcher time, and high trial engagement. When invited, as part of trial participation, to install a smoking cessation app, most participants are likely to do so, and, for those using Quit Sense, an estimated one-half will engage with it for more than 1 week. Evidence that Quit Sense may increase verified abstinence at 6-month follow-up, relative to usual care, was generated, although low saliva return rates to verify smoking status contributed to considerable imprecision in the effect size estimate.

摘要

简介

从吸烟者的环境中习得的吸烟线索是导致复发和复吸的主要原因。Quit Sense 是一款基于理论的即时自适应干预智能手机应用程序,旨在帮助吸烟者了解他们的情境吸烟线索,并在戒烟时提供即时支持以帮助应对这些线索。

方法

这是一项两臂可行性随机对照试验(N=209),旨在估计参数以提供明确评估的信息。通过在线付费广告招募愿意尝试戒烟的吸烟者,并随机分配到“常规护理”(短信转介到 NHS SmokeFree 网站)或“常规护理”加邀请安装 Quit Sense 的短信。除了对无应答者进行手动随访外,其他程序都是自动化的。6 周和 6 个月的随访包括可行性、干预参与度、与吸烟相关的结果和经济结果。通过邮寄唾液样本进行可替宁检测来验证戒烟情况。

结果

6 个月时自我报告的戒烟结果完成率为 77%(95%CI 71%,82%),可行的唾液样本回收率为 39%(95%CI 24%,54%),健康经济数据回收率为 70%(95%CI 64%,77%)。在 Quit Sense 参与者中,75%(95%CI 67%,83%)安装了该应用程序并设定了戒烟日期,其中 51%的参与者使用时间超过一周。6 个月时生物化学验证的持续戒烟率(确定试验的主要预期结果),Quit Sense 组为 11.5%(12/104),常规护理组为 2.9%(3/105)(调整后的优势比=4.57,95%CI 1.23,16.94)。没有发现假设的作用机制存在组间差异的证据。

结论

该研究证明了评估的可行性,并提供了 Quit Sense 有效性的证据。

意义

最初使用主要自动化试验来评估 Quit Sense 是可行的,这导致了适度的招募成本和研究人员的时间投入,以及高试验参与度。当被邀请(作为试验参与的一部分)安装戒烟应用程序时,大多数参与者可能会这样做,并且对于使用 Quit Sense 的参与者,大约有一半会使用该应用程序超过 1 周。与常规护理相比,Quit Sense 可能会增加 6 个月随访时的经证实的戒烟率,这一点得到了证实,尽管吸烟状态的唾液样本回收率较低导致效应大小估计存在相当大的不准确性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5591/10256891/ec2052e87580/ntad032_fig1.jpg

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