Chen Si-Jing, Ivers Hans, Dang-Vu Thien Thanh, Shapiro Colin M, Carney Colleen E, Robillard Rébecca, Morin Charles M
École de Psychologie, Université Laval, 2325 Rue Des Bibliothèques, Québec, Québec, G1V 0A6, Canada.
Centre de recherche CERVO/Brain Research Center, 2301 Av. D'Estimauville, Québec, Québec, G1E 1T2, Canada.
BMC Psychiatry. 2025 May 9;25(1):470. doi: 10.1186/s12888-025-06878-1.
Insomnia is a prevalent yet under-characterized disorder, particularly regarding the heterogeneity of patients and their associated responses to different treatment modalities. This often leads to suboptimal management. There is a need to consider personalized approaches tailored to the characteristics of insomnia phenotypes with regard to objective evidence of shortened sleep duration (< 6 h). This study will examine whether there is a differential treatment response to cognitive behavioral therapy for insomnia (CBT-I) versus pharmacotherapy (lemborexant) as a function of insomnia phenotypes (i.e., ± 6 h of sleep).
This study is a three-arm pragmatic randomized clinical trial, which will enroll 90 adults with chronic insomnia disorder and anxiety/depressive symptoms. Eligible participants will be randomized to one of three conditions (1:1:1) involving CBT-I, lemborexant (Dual Orexin Receptor Antagonist) or placebo medication. Treatment outcomes will be assessed at post-treatment and 6-month follow-up. Insomnia symptom severity as measured by the Insomnia Severity Index will serve as the primary outcome for treatment comparisons. Secondary outcomes will include daily sleep/wake variables derived from the Consensus Sleep Diary, subjective measures of fatigue, mood, mental well-being, functional impairments, and sleep-related beliefs and attitudes. In addition, changes in cognitive performance will be examined as an exploratory outcome. Sleep reactivity and arousal level will be evaluated as potential mediators of treatment-related changes in CBT-I and pharmacotherapy.
This study will contribute to the development of personalized medicine for managing different insomnia phenotypes and will have implication for knowledge mobilization of sleep research.
ClinicalTrials.gov. Identifier: NCT06779149. Registered on 12 January 2025.
失眠是一种常见但特征描述不足的疾病,尤其是在患者的异质性及其对不同治疗方式的相关反应方面。这往往导致治疗效果欠佳。有必要考虑根据失眠表型的特征采取个性化方法,同时要有睡眠时长缩短(<6小时)的客观证据。本研究将探讨失眠表型(即睡眠时长±6小时)对失眠认知行为疗法(CBT-I)与药物疗法(伦博瑞生)的治疗反应是否存在差异。
本研究是一项三臂实用随机临床试验,将招募90名患有慢性失眠症且伴有焦虑/抑郁症状的成年人。符合条件的参与者将被随机分配到三种情况之一(1:1:1),即接受CBT-I、伦博瑞生(双食欲素受体拮抗剂)或安慰剂治疗。治疗结果将在治疗后和6个月随访时进行评估。以失眠严重程度指数衡量的失眠症状严重程度将作为治疗比较的主要结果。次要结果将包括来自共识睡眠日记的每日睡眠/觉醒变量、疲劳、情绪、心理健康、功能损害以及与睡眠相关的信念和态度的主观测量。此外,认知表现的变化将作为探索性结果进行研究。睡眠反应性和唤醒水平将被评估为CBT-I和药物疗法中与治疗相关变化的潜在调节因素。
本研究将有助于开发针对不同失眠表型的个性化药物,并将对睡眠研究的知识传播产生影响。
ClinicalTrials.gov。标识符:NCT06779149。于2025年1月12日注册。