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临床试验/NCT03724474
NCT03724474Unknown不适用

Integrating Mobile and Wearable Technology to Promote Physical Activity and Sleep Among Midlife Adults: the Bio-Behavioral Systems to Motivate and Reinforce Heart Health (BeSMART) Trial

University of Delaware0 个研究点目标入组 60 人开始时间: 2018年11月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
60
主要终点
Change in weekly minutes of moderate-to-vigorous physical activity over 12 weeks

研究概览

简要总结

This study aims to increase weekly minutes of moderate-to-vigorous physical activity and improve sleep quality in a sample of mid-life adults between ages 50 and 64 years.

详细描述

This 2-year study will develop, test, and refine a cloud-based feedback system, and evaluate the impact of a 3 month randomized controlled feasibility pilot intervention - the Bio-behavioral systems to Motivate and Reinforce Heart Health trial (Be SMART) on changes in moderate-to-vigorous physical activity (MVPA) and sleep among mid-life adults between ages 50 and 64 years.

Aim 1 will examine the acceptability of the Be SMART system. We will conduct a 6-week proof- of-concept study in 10 mid-life adults to specifically examine recruitment plausibility, adherence and attrition rates, satisfaction, and implementation fidelity.

Aim 2 will quantify the impact of the Be SMART intervention (n=30) on changes in MVPA and sleep metrics compared to a Fitbit-only condition (n=30) among mid-life adults (N=60). Hypothesis 2a: At 3 months, participants in the Be SMART condition will show significantly greater weekly minutes of MVPA compared to the Fitbit-only condition, controlling for baseline. Hypothesis 2b: At 3 months, participants in the Be SMART condition will be significantly more likely to report adequate sleep duration, shorter sleep latency, and earlier sleep timing, compared to the Fitbit-only condition, controlling for baseline.

Aim 3 will explore the extent to which changes in MVPA and sleep metrics impact blood pressure changes among mid-life adults (N=60). Secondly, this study will quantify the extent to which Be SMART participants (n=30) achieve their weekly goals and if goal achievement impacts changes in blood pressure at 3 months. Hypothesis 3a: Changes in MVPA and sleep metrics will be related to changes in blood pressure. Hypothesis 3b, the degree of goal achievement will be related to changes in blood pressure.

研究设计

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

入排标准

年龄范围
50 Years 至 64 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 50-64 years of age
  • Prehypertensive (120/80 mmHg - 139/89 mmHg) or stage 1 hypertensive (140/90 mmHg - 159/99 mmHg)
  • Physically inactive (<100 minutes of MVPA in the previous week)
  • Report insufficient sleep duration (<6 hours/night on >7 nights in the past month)
  • Own a smartphone
  • Non-smoker
  • No signs or symptoms of chronic disease
  • Have no chronic pain
  • Have no major depressive disorder, general anxiety disorder, or sleep disorder
  • Do not work alternating day-night shifts
  • Medical clearance obtained from individual's physician

排除标准

  • Younger than 50 years; older than 64 years
  • Not prehypertensive or blood pressure is >159/99 mmHg
  • Physically active (>100 min of MVPA in the previous week)
  • Report sufficient sleep duration (>6 hours/night on 7 or more nights in the past month)
  • Does not own a smartphone
  • Current smoker
  • Report signs/symptoms of chronic disease
  • Experiences chronic pain
  • Have major depressive disorder, general anxiety disorder, or sleep disorder
  • Works alternating day and night shifts
  • Medical clearance not obtained from individual's physician

研究组 & 干预措施

Be SMART Condition

Experimental

Subjects randomly assigned to the Be SMART condition (n=30) will first meet with a credentialed health coach to help create personally relevant weekly, short-term (6-weeks) and long-term (12-weeks) PA and sleep goals, and an initial action and coping plan. At 6- weeks (study mid-point), Be SMART subjects will complete a short telephonic "booster" session with the health coach. Throughout the 12-week intervention, our agent-based feedback system will communicate weekly messages via short message service (SMS) based on their weekly goal achievement, informed by the continuous collection of their Fitbit data. In addition, subjects in the Be SMART condition will also take their morning blood pressure using a blue-tooth enabled device that wirelessly sends this data to the Be SMART server.

干预措施: Be SMART (Behavioral)

Fitbit Only Condition

Active Comparator

Subjects who are randomly assigned to the active control condition (n=30) will receive a Fitbit device and wireless blood pressure monitor (same as Be SMART condition). However, subjects in the Fitbit Only condition will not meet with a health coach for establishing SMART goals and creating an action/coping plan, nor will Fitbit Only subjects receive any feedback messages or prompts from the Be SMART server, although data from their Fitbit devices will be continuously collected throughout the q12 week intervention.

干预措施: Be SMART (Behavioral)

结局指标

主要结局

Change in weekly minutes of moderate-to-vigorous physical activity over 12 weeks

时间窗: 12 weeks

Participants will wear an accelerometer for 7 consecutive days at baseline and 12 weeks to assess physical activity intensity (e.g. light, moderate, vigorous)

次要结局

未报告次要终点

研究者

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

Greg Dominick

Associate Professor

University of Delaware

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