针对慢性疼痛和失眠患者的数字化认知行为疗法(CBT-I) (The Back2Sleep Trial):随机对照试验的研究方案。

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Trials Pub Date : 2025-08-15 DOI:10.1186/s13063-025-09013-3
Maria Louise Stage Olsen, Jonas Bloch Thorlund, Robert Zachariae, Werner Vach, Laila Bendix, Julie Jespersen, Preben Kidmose, Christine Parsons, Kristian Kidholm, Henrik Bjarke Vægter
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引用次数: 0

摘要

背景:超过一半的慢性疼痛患者也会失眠。认知行为疗法(CBT-I)是一种有效、安全的失眠一线治疗方法;然而,获取仍然是广泛实施的主要障碍。本研究旨在评估应用程序提供的为期9周的CBT-I干预的有效性,与应用程序提供的睡眠卫生教育计划(主动控制)相比,在减少致残性慢性疼痛和共病性失眠患者的失眠和疼痛严重程度方面。方法:该试验采用1:1随机、单盲、优势试验,随机选取160例致残慢性疼痛伴失眠患者,分别接受应用程序提供的CBT-I治疗9周,或应用程序提供的睡眠卫生教育9周。主要结局是失眠严重指数(ISI)和平均疼痛强度变化的组间差异,使用0-10数值评定量表(NRS)从基线到干预后进行评估。干预后的短期次要结局包括对睡眠和疼痛的感知效应(全球感知效应量表)、睡眠质量、关于睡眠和疼痛的想法和信念、身心健康和EQ5D-5L。中期和长期次要结局(ISI、疼痛强度、EQ5D-5L、医疗费用、睡眠和止痛药的使用)将在24周和52周后收集。探索性生理睡眠指标将从家中耳脑电图(EEG)收集5个晚上的基线和第8周的5个晚上。讨论:这项计划中的研究解决了对慢性疼痛和失眠患者确定有效、安全、易于获得的替代疗法的关键需求。试验注册:ClinicalTrials.gov NCT06361914。于2024年4月17日注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Digitally delivered cognitive behavioral therapy for insomnia (CBT-I) for patients with chronic pain and insomnia (The Back2Sleep Trial): study protocol for a randomized controlled trial.

Background: More than half of individuals with chronic pain also experience insomnia. Cognitive behavioral therapy for insomnia (CBT-I) is an effective and safe first-line treatment; however, access remains a major barrier to widespread implementation. This study aims to evaluate the effectiveness of a 9-week app-delivered CBT-I intervention, compared to an app-delivered sleep hygiene education program (active control), in reducing insomnia and pain severity in patients with disabling chronic pain and comorbid insomnia.

Methods: The trial is a 1:1 randomized, single-blind, superiority trial randomizing 160 patients with disabling chronic pain and comorbid insomnia to either app-delivered CBT-I for 9 weeks or app-delivered sleep hygiene education for 9 weeks. Primary outcomes are the between-group differences in change in Insomnia Severity Index (ISI) and average pain intensity assessed using a 0-10 numeric rating scale (NRS) from baseline to post-interventions. Short-term secondary outcomes post-intervention include perceived effects on sleep and pain (Global Perceived Effect scales), sleep quality, thoughts and beliefs about sleep and pain, physical and mental health, and EQ5D-5L. Medium-term and long-term secondary outcomes (ISI, pain intensity, EQ5D-5L, health care costs, and use of sleep and pain medication) will be collected after 24 and 52 weeks. Exploratory physiological sleep metrics from at-home ear-electroencephalography (EEG) will be collected for five nights at baseline and for five nights during week 8.

Discussion: This planned study addresses a critical need for identifying effective, safe, and easily accessible alternatives to the current treatments for patients with chronic pain and insomnia.

Trial registration: ClinicalTrials.gov NCT06361914. Registered on April 17, 2024.

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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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