Random Assignment of Intervention Messages for Developing Personalized Decision Rules to Promote Physical Activity (RandomAIM)
2022年10月7日 更新者:David E Conroy、Penn State University
Phase 1 Clinical Trial to Develop a Personalized Adaptive Text Message Intervention Using Control Systems Engineering Tools to Increase Physical Activity in Early Adulthood
Our goal is to develop personalized decision rules for selecting the frequency, timing, and content of messages to promote physical activity.
The objective of this project is to develop personalized dynamical models of physical activity (PA) under different weather and temporal conditions as well as in response to different types of intervention messages.
This approach relies on having extensive observations within the person under varying conditions to develop a dynamical model of how different conditions interact with each other to predict how behavior changes in response to text messages.
Complementary sub-models will be estimated for each participant to describe their behavioral responses under different weather conditions.
Healthy but insufficiently active young adults (n=80) will wear an activity monitor and receive a variety of randomly-timed and randomly-selected notifications via smartphone.
GPS coordinates at the time of messages delivery and receipt are recorded and used to look up weather indices at that location at that time.
The work is exploratory/descriptive as we will be developing models to describe participants' responses to messages under different weather conditions.
This work is needed to develop the decision rules for a subsequent behavioral intervention that will be developed and tested in a future project.
研究概览
研究类型
介入性
注册 (实际的)
82
阶段
- 阶段1
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
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Pennsylvania
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University Park、Pennsylvania、美国、16802
- The Pennsylvania State University
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参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 至 29年 (成人)
接受健康志愿者
是的
有资格学习的性别
全部
描述
Inclusion Criteria:
- Participants capable of reading, speaking and understanding English and of giving informed consent.
- Participants between the ages of 18-29 years.
- Participants must be free of visual impairment that would interfere with the use of a smartphone.
- Participants must own and carry an iPhone (running iOS version 10 or higher) or Android (running operating system 7 or higher) smartphone during waking hours.
Exclusion Criteria:
- Participants engaging in 90 or more minutes of moderate- or greater intensity PA each week.
- Participants engaged in organized programs with mandated physical activity (e.g., varsity sports, ROTC).
- Participants with contraindications to normal physical activity on the Physical Activity Readiness Questionnaire.
- Participants who require an assistive device for mobility or have any other condition that may limit or prevent participation in moderate-intensity physical activity.
- Participants who are pregnant or planning to become pregnant within the next 6 months.
- Participants with a prior diagnosis of cancer, cardiovascular disease, diabetes or metabolic syndrome.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:预防
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:Random Messaging
Participants receive 0-5 messages/day from the Random AIM app.
Messages are only delivered outside of a participant-specific Do Not Disturb window (e.g., 11pm-8am).
Messages are selected randomly from three content domains: Move More (40%), Sit Less (40%), and Inspirational Quotes Unrelated to Movement (20%).
Half of the messages are accompanied by images.
Message selection and timing are determined randomly each night for the following day.
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Messages can be up to 256 characters of text and with or without an image.
"Move more" and "sit less" messages were written to target established cognitive and affective constructs associated with physical activity (e.g., prompts to action plan, guidance for maximizing pleasure by regulating intensity).
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Change in Moderate (or Higher) Physical Activity Duration Following Message Receipt
大体时间:15-minute epochs for the remainder of the walking day
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Fitbit-assessed minutes with step counts >= 100 steps/min in 15-minute epochs (steady states represent the change in expected step counts if a message was delivered versus if the message was not delivered)
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15-minute epochs for the remainder of the walking day
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员:David E Conroy, PhD、The Pennsylvania State University
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2019年4月3日
初级完成 (实际的)
2020年7月21日
研究完成 (实际的)
2020年7月21日
研究注册日期
首次提交
2019年4月5日
首先提交符合 QC 标准的
2019年4月5日
首次发布 (实际的)
2019年4月9日
研究记录更新
最后更新发布 (实际的)
2022年11月4日
上次提交的符合 QC 标准的更新
2022年10月7日
最后验证
2022年10月1日
更多信息
与本研究相关的术语
其他研究编号
- STUDY00009455
- R01HL142732 (美国 NIH 拨款/合同)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
不
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.