基于app的年轻人吸烟冲动减少干预:结合微随机试验和常规受试者间随机试验的方案。

IF 1.5 Q3 HEALTH CARE SCIENCES & SERVICES
Johannes Thrul, Janardan Devkota, Joseph J C Waring, Michael R Desjardins, Josef Hamoud, Jasmin Han, Felix Naughton, Vadim Zipunnikov, Tamar Mendelson, Carl Latkin, David Epstein, Meghan Moran
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引用次数: 0

摘要

背景:吸烟是美国发病率和死亡率的主要可预防原因,年轻人的吸烟率很高。虽然大多数年轻成年吸烟者对戒烟感兴趣,但他们没有充分利用专业戒烟支持。智能手机已经广泛地融入了年轻人的生活,这些设备提供了很好的机会来提供戒烟干预措施,当吸烟者需要戒烟支持时,它们可以“在当下”提供建议应对策略的信息。目的:本试验的总体目标是评估认知行为疗法(CBT)和正念或接受和承诺疗法(ACT)信息对针对特定高危吸烟情况的年轻人的疗效。方法:我们将进行一项微随机试验(MRT;受试者内随机化),以测试CBT和正念或ACT在信息传递后15分钟内与对照信息相比减少吸烟冲动的效果,该试验采用常规的受试者间随机对照试验(RCT)。传统的受试者间对照组参与者将只完成生态瞬时评估(EMA),而不提供干预信息,这将使我们能够在治疗结束、3个月随访和6个月随访时测试信息是否减少了每天的吸烟量。在MRT干预组参与者中,我们将探索共同使用物质(大麻,酒精,其他药物)和暴露于特定环境(家庭,工作,酒吧)如何调节信息功效。结果:截至2025年6月,我们招募了目标样本160名中的58名参与者,其中52%(30/58)分配给MRT组,48%(28/58)分配给仅接受ema治疗的对照组。结论:现在吸烟在年轻人中比在青少年中更常见,早期戒烟大大降低了吸烟的发病率和死亡率,因此对这一高优先人群进行适龄、量身定制和可扩展的干预变得更加重要。这项试验的结果将为量身定制的干预信息的有效性提供证据,帮助年轻的成年吸烟者应对吸烟冲动,作为智能手机干预的一个组成部分。调查结果将使该领域了解基于应用程序的减少烟草使用冲动信息的关键原则、策略和效果。试验注册:ClinicalTrials.gov NCT05836103;https://clinicaltrials.gov/study/NCT05836103.International注册报告标识符(irrid): DERR1-10.2196/74388。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

App-Based Smoking Urge Reduction Intervention for Young Adults: Protocol Combining a Microrandomized Trial and Conventional Between-Subject Randomized Trial.

App-Based Smoking Urge Reduction Intervention for Young Adults: Protocol Combining a Microrandomized Trial and Conventional Between-Subject Randomized Trial.

App-Based Smoking Urge Reduction Intervention for Young Adults: Protocol Combining a Microrandomized Trial and Conventional Between-Subject Randomized Trial.

App-Based Smoking Urge Reduction Intervention for Young Adults: Protocol Combining a Microrandomized Trial and Conventional Between-Subject Randomized Trial.

Background: Tobacco smoking is the leading preventable cause of morbidity and mortality in the United States, and young adults have high smoking rates. Although most young adult smokers are interested in quitting, they underutilize professional cessation support. Smartphones have wide reach and integration into young adults' lives, and these devices offer great opportunities to deliver cessation interventions by delivering messages suggesting coping strategies "in the moment" when smokers need cessation support.

Objective: The overall goal of this trial is to evaluate the efficacy of cognitive behavioral therapy (CBT) and mindfulness or acceptance and commitment therapy (ACT) messages for young adults targeted at specific high-risk situations for smoking.

Methods: We will conduct a microrandomized trial (MRT; within-subject randomization) to test the efficacy of CBT and mindfulness or ACT compared with control messages for reducing smoking urge up to 15 minutes after message delivery, nested in a conventional between-subject randomized controlled trial (RCT). A conventional between-subject control group of participants who will complete ecological momentary assessment (EMA) only without intervention messages will allow us to test if messages reduce cigarettes per day at the end of treatment, 3-month follow-up, and 6-month follow-up. Among MRT intervention group participants, we will explore how message efficacy may be moderated by substance co-use (cannabis, alcohol, other drugs) and exposure to specific settings (home, work, bars).

Results: As of June 2025, we had enrolled 58 participants of the target sample of 160, with 52% (30/58) assigned to the MRT group and 48% (28/58) assigned to the EMA-only control.

Conclusions: Smoking onset is now more common among young adults than adolescents, and early cessation substantially reduces morbidity and mortality from smoking, making age-appropriate, tailored, and scalable interventions for this high-priority population even more important. Results of this trial will provide evidence on the efficacy of tailored intervention messages to help young adult smokers cope with smoking urges as an integral part of smartphone interventions. Findings will inform the field about key principles, strategies, and efficacy of situational tailoring of app-based tobacco use urge reduction messages.

Trial registration: ClinicalTrials.gov NCT05836103; https://clinicaltrials.gov/study/NCT05836103.

International registered report identifier (irrid): DERR1-10.2196/74388.

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来源期刊
CiteScore
2.40
自引率
5.90%
发文量
414
审稿时长
12 weeks
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