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临床试验/NCT04962087
NCT04962087招募中不适用

Randomized Controlled Trial to Evaluate Health enSuite Insomnia: an App-based Treatment for Adult Chronic Insomnia

IWK Health Centre2 个研究点 分布在 1 个国家目标入组 415 人开始时间: 2024年8月29日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
415
试验地点
2
主要终点
Change in Insomnia Severity Index (ISI) Score

研究概览

简要总结

This project consists of a randomized controlled trial. The objective of this trial is to test the effectiveness of an app-based cognitive behavioral program for insomnia (Health enSuite: Insomnia) in reducing insomnia symptoms.

详细描述

Insomnia or insufficient sleep is one of the most prevalent public health issues. Nearly 1 in 4 Canadians over the age of 18 years report having difficulty falling asleep or maintaining sleep, the majority of whom have experienced these insomnia symptoms for more than a year. Chronic insomnia is characterized by one or more of the following symptoms occurring for at least three nights per week for at least 3 months: difficulty falling asleep, trouble maintaining sleep, difficulty in getting back to sleep, poor quality of sleep, and waking up too early the next morning. These symptoms persist despite adequate opportunity for sleep and are accompanied by significant impairments in daytime functioning.

Cognitive behavioral therapy for insomnia (CBT-I) is a multi-component intervention approach that is recommended as the first line of treatment for patients with persistent insomnia. It targets beliefs, thoughts, and expectations related to sleep as well as behavioral factors that result in sleep loss (sleep schedules, caffeine intake prior to bedtime, bright light in bedroom). These interventions have been found to improve the quality and the duration of sleep and improve daytime functioning. Despite the efficacy of CBT-I programs, they are not readily available to most patients. Therefore, our goal is to develop a CBT-I program that can be delivered through an internet connected phone, tablet, or computer and provide effective treatment to a wide range of people with chronic insomnia. Given that many individuals seek help for sleep problems online or face barriers accessing in-person care, internet-based CBT-I offers a scalable and accessible solution for those experiencing chronic insomnia.

Sleep medications are commonly used to manage insomnia symptoms. These include benzodiazepines such as temazepam and non-benzodiazepines like zopiclone, zolpidem, and zaleplon (often referred to as "Z drugs"). While these benzodiazepine receptor agonists (BZRAs) can be effective in the short term, long-term use is associated with diminishing benefits and potential risks, such as side effects, dependence, and-particularly in older adults-falls and cognitive impairment. Given these concerns, there is growing recognition of the importance of expanding access to non-pharmacological, evidence-based treatments for insomnia. Cognitive behavioral therapy for insomnia (CBT-I) is one such approach, but it remains underutilized due to limited availability. A widely accessible, app-based CBT-I program has the potential to fill this gap and offer a safer, long-term solution for individuals struggling with chronic insomnia.

This project consists of a randomized controlled trial. The objective of this trial is to test the effectiveness of an app-based cognitive behavioral program for insomnia (Health enSuite: Insomnia) in reducing insomnia symptoms.

The objectives will be to assess the effectiveness of CBT-I delivered through the Health enSuite app in:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Change in Insomnia Severity Index (ISI) Score

时间窗: Baseline assessment, 2 months post-randomization, 5 months post-randomization

The ISI is a 7-item questionnaire measuring insomnia severity, dissatisfaction with sleep, interference with daily functioning, and daytime impairment. Scores range from 0-28, with higher scores indicating more severe insomnia.

次要结局

  • Change in Sleep Efficiency(Baseline assessment, 2 months post-randomization, 5 months post-randomization)
  • Change in Sleep Onset Latency(Baseline assessment, 2 months post-randomization, 5 months post-randomization)
  • Change in Wake After Sleep Onset (WASO)(Baseline assessment, 2 months post-randomization, 5 months post-randomization)
  • Change in Depression, Anxiety, and Stress Scores (DASS-21)(Baseline assessment, 2 months post-randomization, 5 months post-randomization)
  • Change in Sleep Efficiency(Baseline assessment, 2 months post-randomization, 5 months post-randomization)
  • Change in Total Sleep Time(Baseline assessment, 2 months post-randomization, 5 months post-randomization)
  • Change in Sleep Onset Latency(Baseline assessment, 2 months post-randomization, 5 months post-randomization)
  • Change in Wake After Sleep Onset (WASO)(Baseline assessment, 2 months post-randomization, 5 months post-randomization)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Patrick J. McGrath

Principal Investigator

IWK Health Centre

研究点 (2)

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