数字治疗酒精依赖的有效性和安全性:一项多中心、开放标签、随机对照试验

IF 6.2 3区 医学 Q1 CLINICAL NEUROLOGY
Psychiatry and Clinical Neurosciences Pub Date : 2025-10-01 Epub Date: 2025-07-28 DOI:10.1111/pcn.13874
Ryuhei So, Kazuhiro Nouso, Sachio Matsushita, Hitoshi Yoshiji, Takefumi Yuzuriha, Eisuke Hida, Hiroki Nishimura, Yusuke Takagi, Yoshinori Horie
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引用次数: 0

摘要

目的:数字疗法(DTx)是一种新兴的治疗方式,通过软件程序(如智能手机应用程序)加强心理社会干预。我们开发了一个名为ALM-003的DTx,以支持那些追求减少饮酒目标的酒精依赖者的治疗。ALM-003旨在通过个性化反馈、交互式心理教育模块和患者和医生的自动化治疗支持工具的日常自我监测来促进行为改变。在这项多中心、开放标签、随机对照试验(RCT)中,我们旨在评估ALM-003在各种临床环境中的疗效和安全性。方法:在这项随机对照试验中,没有因过度饮酒而出现严重身体、精神或社会问题的酒精依赖者,以及表现出高或非常高饮酒风险水平的参与者被随机分为干预组(通过ALM-003增强的社会心理干预)和对照组(使用基本饮酒日记应用程序的社会心理干预),为期24周。主要结局是28天内(第0周至第12周)重度饮酒天数(hdd)的变化。结果:对136名干预者和142名对照者的主要结局进行了数据分析。干预组和对照组的基线hdd分别为19.4天和19.1天/28天。在第12周,干预组和对照组的hdd较基线分别减少了-12.2天和-9.5天,组间差异为-2.79天/28天(95%可信区间:-4.67至-0.90;p = 0.004)。干预组不良事件发生率为32.9%,对照组为33.6%。没有不良事件归因于应用程序的使用。结论:ALM-003在高或非常高饮酒风险的酒精依赖人群中显示出减少重度饮酒天数的功效。临床试验注册:该试验设计已在日本临床试验注册中心(jRCT) (https://jrct.niph.go.jp/)前瞻性注册。试验标识符为jRCT2032220560。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Efficacy and safety of a digital therapeutic for alcohol dependence: A multicenter, open-label, randomized controlled trial.

Efficacy and safety of a digital therapeutic for alcohol dependence: A multicenter, open-label, randomized controlled trial.

Efficacy and safety of a digital therapeutic for alcohol dependence: A multicenter, open-label, randomized controlled trial.

Efficacy and safety of a digital therapeutic for alcohol dependence: A multicenter, open-label, randomized controlled trial.

Aim: Digital therapeutics (DTx) is an emerging treatment modality for enhancing psychosocial interventions via software programs, such as smartphone applications (apps). We developed a DTx named ALM-003 to support treatment for people with alcohol dependence who are pursuing reduced drinking goals. ALM-003 was designed to promote behavioral change through daily self-monitoring with personalized feedback, interactive psychoeducational modules, and automated treatment support tools for both patients and physicians. In this multicenter, open-label, randomized controlled trial (RCT), we aimed to evaluate the efficacy and safety of ALM-003 in various clinical settings.

Methods: In this RCT, participants with alcohol dependence without serious physical, mental, or social problems due to excessive drinking, and exhibiting high or very high drinking risk levels were randomized into an intervention group (psychosocial intervention enhanced by ALM-003) or a control group (psychosocial intervention with a basic drinking diary app) for 24 weeks. The primary outcome was the change in the number of heavy drinking days (HDDs) over 28 days (Week 0 to Week 12).

Results: Data analysis of the primary outcome for 136 intervention and 142 control participants was performed. Baseline HDDs were 23.2 and 23.1 days/28 days in the intervention and control groups, respectively. [Correction added on 3 September 2025, after first online publication: The values of the baseline HDDs in the preceding sentence have been corrected from '19.4 and 19.1 days' to '23.2 and 23.1 days'.] At Week 12, the intervention and control groups showed a reduction in HDDs of -12.2 and -9.5 days from baseline, with a between-group difference of -2.79 days/28 days (95% confidence interval: -4.67 to -0.90; P = 0.004). Adverse events occurred in 32.9% of participants in the intervention group and 33.6% in the control group. No adverse events were attributed to app use.

Conclusion: ALM-003 demonstrated efficacy in reducing heavy drinking days among people with alcohol dependence at a high or very high drinking risk.

Clinical trial registration: The trial design was prospectively registered with the Japan Registry of Clinical Trials (jRCT) (https://jrct.niph.go.jp/). The trial identifier is jRCT2032220560.

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来源期刊
CiteScore
7.40
自引率
4.20%
发文量
181
审稿时长
6-12 weeks
期刊介绍: PCN (Psychiatry and Clinical Neurosciences) Publication Frequency: Published 12 online issues a year by JSPN Content Categories: Review Articles Regular Articles Letters to the Editor Peer Review Process: All manuscripts undergo peer review by anonymous reviewers, an Editorial Board Member, and the Editor Publication Criteria: Manuscripts are accepted based on quality, originality, and significance to the readership Authors must confirm that the manuscript has not been published or submitted elsewhere and has been approved by each author
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