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临床试验/NCT04089007
NCT04089007已完成不适用

Feasibility, Acceptability and Effectiveness of the SOmNI (Sleep Outcomes, Mhealth, Wearable Sensors and Nudging Intervention) Mobile Phone App for Sleep Promotion in Adolescents: SOmNI Pilot RCT

University of Toronto2 个研究点 分布在 1 个国家目标入组 65 人开始时间: 2018年1月26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
65
试验地点
2
主要终点
Compliance rate

研究概览

简要总结

This study evaluates the acceptability, feasibility, and efficacy of an intervention using wearable sensors and a mHealth application, SOmNI, to promote sleep for adolescents. The investigators hypothesize that a behavioural intervention delivered through a mobile app will be a cost-effective and accessible method of engaging adolescents in the self-management of sleep behaviours. Participants will be randomized to either the SOmNI Intervention group or the Control group. Participants receiving the SOmNI app will attempt to incrementally move their school night bedtime earlier in the evening.

详细描述

Over 60% of adolescents sleep less than the 9 hours of sleep recommended for 13-18 year olds. Quality of life is reduced due to the daytime consequences of chronic sleep deprivation such as sleepiness, fatigue, low mood, and inattentiveness at school. Although this sleep debt occurs in otherwise healthy adolescents, it significantly increases their risk of development of the chronic health conditions (cardiovascular disease and depression) and forms of accidental injury (motor vehicle accidents) that place the greatest demands on our health care system. Despite increased recognition of adequate sleep as a key contributor to health, there exist few effective interventions to promote sleep in adolescents. This study is designed to determine compliance, feasibility and preliminary data on health outcomes (nocturnal sleep measured objectively by actigraphy; daytime sleepiness; anxiety; depression; unintentional injuries; morning school attendance). This study will be a pilot RCT, randomizing 76 adolescents to one of two groups (i.e. 38 per group). Study arms will include a control group and intervention group (activity monitoring device with custom application). Mobile health, user-friendly low-intensity interventions with wearable sleep sensors and tailored feedback may help many adolescents to increase the amount of sleep they achieve.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
13 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • enrolled in high school (grades 9 to 12)
  • ages 13-17 years
  • report sleeping <8 hours per weeknight (Sun-Thurs)
  • endorse daytime sleepiness that interferes with their daily function to a moderate or severe degree (e.g. To what extent do you consider your sleepiness to interfere with your daily functioning (e.g. daytime fatigue, mood, ability to function at school, concentration, memory)
  • report sleeping >9 hours on weekend nights (Fri-Sat)
  • have either their own iPhone (version 4S or higher) or are willing to use a study-provided iPhone

排除标准

  • developmental delay (e.g. more than one grade level beyond what is appropriate for age)
  • physician-diagnosed, significant physical health problem (e.g. cystic fibrosis, diabetes, lupus, kidney disease, hypertension, inflammatory bowel disease, etc)
  • physician-diagnosed mental health problem (e.g. anxiety, depression, ADHD),
  • physician-diagnosed sleep disorder (e.g. narcolepsy, obstructive sleep apnea, insomnia, restless leg syndrome)
  • suspected sleep disordered breathing problem as identified by screening with questions from the Pediatric Sleep Questionnaire
  • suspected insomnia based on screening with questions from the Insomnia Severity Index
  • suspected Restless Leg Syndrome based on screening with the International RLS Study Group questionnaire
  • suspected delayed sleep phase syndrome as evidenced by consistent inability to fall asleep before 01h00 to 06h00, significant impairment in the ability to attend school due to extreme delay of their sleep schedule, and avoidance of other social or family functions in the daytime

结局指标

主要结局

Compliance rate

时间窗: Through study completion, an average of 6 weeks

Compliance rate (percentage of participants assigned to intervention group who used SOMNI app to monitor sleep)

Dropout rate

时间窗: Through study completion, an average of 6 weeks

Dropout rate (percentage of participants who withdrew from the study groups)

次要结局

  • Recruitment rate(Through study completion, an average of 6 weeks)
  • Data completion rates(Through study completion, an average of 6 weeks)

研究者

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

Robyn Stremler

Associate Professor

University of Toronto

研究点 (2)

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