VA Rocky Mountain Mental Illness Research Education and Clinical Center (MIRECC), Rocky Mountain Regional VA Medical Center (RMRVAMC), Aurora, CO, United States; Department of Physical Medicine & Rehabilitation, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
VA Rocky Mountain Mental Illness Research Education and Clinical Center (MIRECC), Rocky Mountain Regional VA Medical Center (RMRVAMC), Aurora, CO, United States; Department of Psychiatry, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Contemp Clin Trials. 2024 Jun;141:107525. doi: 10.1016/j.cct.2024.107525. Epub 2024 Apr 9.
Individuals with a history of moderate-severe traumatic brain injury (TBI) experience a significantly higher prevalence of insomnia compared to the general population. While individuals living with TBI have been shown to benefit from traditional insomnia interventions (e.g., face-to-face [F2F]), such as Cognitive Behavioral Therapy for Insomnia (CBTI), many barriers exist that limit access to F2F evidence-based treatments. Although computerized CBT-I (CCBT-I) is efficacious in terms of reducing insomnia symptoms, individuals with moderate-severe TBI may require support to engage in such treatment. Here we describe the rationale, design, and methods of a randomized controlled trial (RCT) assessing the efficacy of a guided CCBT-I program for reducing insomnia symptoms for participants with a history of moderate-severe TBI.
This is an RCT of a guided CCBT-I intervention for individuals with a history of moderate-severe TBI and insomnia. The primary outcome is self-reported insomnia severity, pre- to post-intervention. Exploratory outcomes include changes in sleep misperception following CCBT-I and describing the nature of guidance needed by the Study Clinician during the intervention.
This study represents an innovative approach to facilitating broader engagement with an evidence-based online treatment for insomnia among those with a history of moderate-severe TBI. Findings will provide evidence for the level and nature of support needed to implement guided CCBT-I. Should findings be positive, this study would provide support for a strategy by which to deliver guided CCBT-I to individuals with a history of moderate-severe TBI.
与一般人群相比,有中度至重度创伤性脑损伤 (TBI) 病史的个体失眠的患病率明显更高。虽然已经证明生活在 TBI 中的个体从传统的失眠干预措施(例如面对面 [F2F])中受益,例如失眠认知行为疗法 (CBTI),但存在许多限制获得 F2F 循证治疗的障碍。尽管计算机化 CBT-I (CCBT-I) 在减轻失眠症状方面是有效的,但中度至重度 TBI 个体可能需要支持来参与此类治疗。在这里,我们描述了一项随机对照试验 (RCT) 的原理、设计和方法,该试验评估了针对有中度至重度 TBI 病史和失眠的参与者的指导 CCBT-I 计划减少失眠症状的疗效。
这是一项针对有中度至重度 TBI 和失眠病史的个体的指导 CCBT-I 干预的 RCT。主要结局是自我报告的失眠严重程度,干预前后。探索性结局包括 CCBT-I 后睡眠错觉的变化以及描述研究临床医生在干预过程中需要的指导的性质。
这项研究代表了一种创新方法,可以促进更多有中度至重度 TBI 病史的人更广泛地参与基于证据的在线失眠治疗。研究结果将为实施指导 CCBT-I 所需的支持水平和性质提供证据。如果研究结果为阳性,这项研究将为向有中度至重度 TBI 病史的个体提供指导 CCBT-I 的策略提供支持。