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临床试验/NCT05067569
NCT05067569已完成不适用

App-delivered Sleep ThERapy for Older Individuals With Insomnia (ASTEROID Study)

Woolcock Institute of Medical Research2 个研究点 分布在 1 个国家目标入组 270 人开始时间: 2022年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
270
试验地点
2
主要终点
Change in insomnia symptom severity

研究概览

简要总结

This randomised, open, parallel controlled trial aims to compare the efficacy of a digital brief behavioural therapy for insomnia (dBBTi) against online sleep health education on insomnia symptom severity in older adults aged 60 years and over. The trial will be totally online with participants recruited from the community across Australia.

详细描述

Insomnia is a highly prevalent sleep disorder affecting up to 10% of the adult population and reports of over 40% in the older population. Current insomnia treatments focus heavily on symptom management with cognitive behavioural therapy for insomnia (CBTi), in both digital and face-to-face form as the recommended first-line treatment. Despite the strong evidence for digital CBTi, there are a lack of data related to older people and whether digital brief behavioural therapy is efficacious in this population.

The investigators will conduct a fully online study comparing 6-weeks of digital brief behavioural therapy for insomnia (dBBTi) against online sleep health education. Participants will be recruited, screened and determined eligibility and consent will be conducted online. Thereafter, participants will be randomly allocated to either dBBTi delivered via a mobile application called SleepFix or wait-listed control. The SleepFix app delivers sleep restriction therapy using a 4 stage approach to improve sleep efficiency. The control will consist of 3 online sleep health education modules provided bi-weekly with information about sleep and sleep hygiene without any specific insomnia therapy. Participants will be recruited using social media and directed to a website to determine eligibility and then provided access to either the dBBTi (SleepFix) or the control with a link to the first online module.

At baseline, all participants will complete self-reported measures of insomnia, sleep, fatigue, sleepiness , anxiety, depression, quality of life, cognition and digital health literacy. These will be repeated at follow-up at weeks 8, 16 and 26.

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
Single (Investigator)

盲法说明

Participants will not be blinded as they will know what treatment they receive. This is typical of behavioural interventions.

Note: the study project coordinator will not be blinded as they will be managing the study such as sending sleep-tracking wearable devices to the intervention arm and communicating with participants. All investigators and data analysts will be blinded.

入排标准

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

入选标准

  • Older adults aged ≥ 60 years
  • Able to give informed online consent
  • Insomnia Severity Index ≥ 10, including a score of 3 in at least one of the first three items (nocturnal symptoms).
  • English fluency
  • Access to a smartphone and willingness/proficiency to use a mobile app

排除标准

  • Shift-workers
  • Travel to a destination with >2 hours time-difference (within 30-days)
  • Serious medical and/or psychiatric illnesses/disorders or self-harm risk (Patient Health Questionnaire-9, item 9, 1+ score of risk of suicidal ideation)
  • Diagnosed sleep disorders other than insomnia
  • Regular sleep medications or sleep devices (>2 times a week over last 6 months)
  • Currently receiving or previously received (within the last 12 months) psychotherapy for insomnia including Cognitive Behavioural Therapy (CBT).
  • Drive for work/operate heavy machinery

结局指标

主要结局

Change in insomnia symptom severity

时间窗: Change score from baseline at 8 weeks

Insomnia Severity Index (ISI) is a 7-item questionnaire used to examine overall insomnia severity. It consists of a five-point Likert type scale for each item (ranging from "no problem" = 0 to "severe problem" = 4) regarding symptoms over the past 2 weeks. Scores range from 0-28 with higher scores indicating greater insomnia symptom severity.

次要结局

  • Change in subjective sleep quality(Change score from baseline at 8 weeks)
  • Change in sleep onset latency(Change score from baseline at 8 weeks)
  • Change in fatigue(Change score from baseline at 8 weeks)
  • Change in daytime sleepiness(Change score from baseline at 8 weeks)
  • Change in quality of Life(Change score from baseline at 8 weeks)
  • Change in self-reported cognition(Change score from baseline at 8 weeks)
  • The effect of baseline digital health literacy on therapy efficacy(Baseline, week 8)
  • Change in wake after sleep onset(Change score from baseline at 8 weeks)
  • Change in total sleep time(Change score from baseline at 8 weeks)
  • Change in depressive symptoms(Change score from baseline at 8 weeks)
  • Change in anxiety(Change score from baseline at 8 weeks)
  • Engagement(Baseline, week 8)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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