高危睡眠呼吸暂停对量身定制的失眠数字认知行为疗法项目治疗反应的影响:准实验性试验

A. Sweetman, C. Reynolds, L. Lack, Andrew Vakulin, C. Chai-Coetzer, Douglas M. Wallace, Megan Crawford, C. Richardson
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摘要

由治疗师提供的失眠认知行为疗法(CBTi)是一种有效的治疗方法,但对于合并失眠和睡眠呼吸暂停(COMISA)患者来说,这种方法基本上难以使用。为了增加COMISA患者接受CBTi治疗的机会,我们旨在开发一种适合失眠症患者和COMISA患者的自助式互动5疗程数字CBTi程序,并比较其在失眠症患者与合并失眠症和高危睡眠呼吸暂停患者之间的疗效。高危睡眠呼吸暂停的定义是 OSA50 分≥5。在基线、8 周和 16 周的随访中,参与者自我报告了失眠症状(ISI)、抑郁、焦虑、嗜睡(ESS)、疲劳和与睡眠相关的不良信念(DBAS-16)。在每次 CBTi 治疗过程中还会评估 ESS 分数。采用意向治疗混合模型和完整病例 chi2 分析。单独失眠的参与者[n = 43,年龄 M (sd) = 51.8 (17.0),86.1% 为女性]多于疑似 COMISA 的参与者[n = 19,年龄 = 54.0 (14.8),73.7% 为女性]。基线问卷数据和随访数据缺失率没有组间差异。在任何结果上,组与组之间都没有明显的时间交互作用。时间的主效应表明,在 16 周时,失眠(d = 3.3)、抑郁(d = 1.2)、焦虑(d = 0.6)、ESS(d = 0.5)、疲劳(d = 1.2)和 DBAS-16 症状(d = 1.2)均有中度至大幅持续改善。这项互动式数字 CBTi 计划对失眠症患者以及合并失眠症和高危睡眠呼吸暂停症的患者都很有效。该试验已在澳大利亚和新西兰临床试验注册中心(ANZCTR,ACTRN12621001395820)进行了前瞻性注册。
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Effect of high-risk sleep apnea on treatment-response to a tailored digital cognitive behavioral therapy for insomnia program: a quasi-experimental trial
Therapist-delivered Cognitive Behavioral Therapy for Insomnia (CBTi) is an effective but largely inaccessible treatment for people with Co-Morbid Insomnia and Sleep Apnea (COMISA). To increase CBTi access for COMISA, we aimed to develop a self-guided interactive 5-session digital CBTi program that is appropriate for people with insomnia-alone and COMISA, and compare its effectiveness between people with insomnia-alone, vs. comorbid insomnia and high-risk sleep apnea.Data from 62 adults with insomnia symptoms were used. High-risk sleep apnea was defined as a score of ≥5 on the OSA50. Participants self-reported symptoms of insomnia (ISI), depression, anxiety, sleepiness (ESS), fatigue, and maladaptive sleep-related beliefs (DBAS-16) at baseline, 8-week, and 16-week follow-up. ESS scores were additionally assessed during each CBTi session. Intent-to-treat mixed models and complete-case chi2 analyses were used.There were more participants with insomnia-alone [n = 43, age M (sd) = 51.8 (17.0), 86.1% female] than suspected COMISA [n = 19, age = 54.0 (14.8), 73.7% female]. There were no between-group differences in baseline questionnaire data, or rates of missing follow-up data. There were no significant group by time interactions on any outcomes. Main effects of time indicated moderate-to-large and sustained improvements in insomnia (d = 3.3), depression (d = 1.2), anxiety (d = 0.6), ESS (d = 0.5), fatigue (d = 1.2), and DBAS-16 symptoms (d = 1.2) at 16-weeks. ESS scores did not increase significantly during any CBTi session.This interactive digital CBTi program is effective in people with insomnia-alone, and people with co-morbid insomnia and high-risk sleep apnea. Further research is required to determine the effectiveness, safety and acceptability of digital CBTi in people with insomnia and confirmed sleep apnea.This trial was prospectively registered on the Australian and New Zealand Clinical Trials Registry (ANZCTR, ACTRN12621001395820).
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