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基于智能手机的认知行为疗法应用程序对失眠的影响:一项随机双盲研究。

Effect of smartphone-based cognitive behavioral therapy app on insomnia: a randomized, double-blind study.

作者信息

Watanabe Yosuke, Kuroki Taiyo, Ichikawa Daisuke, Ozone Motohiro, Uchimura Naohisa, Ueno Taro

机构信息

SUSMED, Inc., Tokyo, Japan.

Department of Neuropsychiatry, Kurume University School of Medicine, Fukuoka, Japan.

出版信息

Sleep. 2023 Mar 9;46(3). doi: 10.1093/sleep/zsac270.

Abstract

STUDY OBJECTIVES

This study assessed the effects and safety of the smartphone-based cognitive behavioral therapy for insomnia (CBT-I) app compared with the sham app.

METHODS

In this multicenter, double-blind, and parallel-group study, 175 patients with insomnia were randomized to a smartphone-based CBT-I app (Active, n = 87) or a sham app (Sham, n = 88) group. The primary endpoint was the change in Athens Insomnia Score (AIS) from baseline after 8 weeks of treatment.

RESULTS

The change in AIS (mean ± standard deviation) from baseline, assessed using a modified-intent-to-treat analysis, was -6.7 ± 4.4 in the Active group and -3.3 ± 4.0 in the Sham group. The difference in the mean change between the groups was -3.4 (p < .001), indicating a greater change in the Active group. The change in CGI-I from the baseline was 1.3 ± 0.8 in the Active group and 0.7 ± 0.8 in the Sham group (p < .001). The proportion of patients with an AIS less than 6 was 37.9% in the Active group and 10.2% in the Sham group (p < .001). As for the safety assessment, no adverse reactions or device failures were detected in the Active group.

CONCLUSIONS

This study demonstrated the effectiveness of a smartphone-based CBT-I system for treating insomnia.

CLINICAL TRIAL REGISTRATION

ID: jRCT2032210071; trial name: Sham (software)-controlled, multicenter, dynamic allocation, double-blinded study of non-medication therapy with a software Yukumi in patients with insomnia disorders (verification study); URL: https://jrct.niph.go.jp/en-latest-detail/jRCT2032210071.

摘要

研究目的

本研究评估了基于智能手机的失眠认知行为疗法(CBT-I)应用程序与模拟应用程序相比的效果和安全性。

方法

在这项多中心、双盲、平行组研究中,175名失眠患者被随机分为基于智能手机的CBT-I应用程序组(干预组,n = 87)或模拟应用程序组(对照组,n = 88)。主要终点是治疗8周后雅典失眠量表(AIS)较基线的变化。

结果

采用改良意向性分析评估,干预组AIS较基线的变化(均值±标准差)为-6.7±4.4,对照组为-3.3±4.0。两组间平均变化的差异为-3.4(p < .001),表明干预组变化更大。干预组CGI-I较基线的变化为1.3±0.8,对照组为0.7±0.8(p < .001)。AIS小于6的患者比例在干预组为37.9%,对照组为10.2%(p < .001)。至于安全性评估,干预组未检测到不良反应或设备故障。

结论

本研究证明了基于智能手机的CBT-I系统治疗失眠的有效性。

临床试验注册

编号:jRCT2032210071;试验名称:Sham(软件)对照、多中心、动态分配、双盲的Yukumi软件非药物治疗失眠症患者的研究(验证研究);网址:https://jrct.niph.go.jp/en-latest-detail/jRCT2032210071

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