Columbia Moves Physical Activity
2018年11月27日 更新者：University of South Carolina
Evaluating Columbia Moves: A Social Network Approach Using a Team Competition and Technology to Increase Physical Activity
The purpose of this study is to evaluate the effect of adding a team competition comprised of members of existing social networks to a technology-delivered program for enhancing physical activity among insufficiently active adults.
研究概览
详细说明
This 3-month randomized controlled trial is designed to investigate the efficacy and feasibility of a novel, technology-oriented physical activity intervention characterized by existing social networks and a team competition.
Participants will be recruited via emails, fliers, and word of mouth.
They will be randomized to a technology-mediated physical activity treatment (TECH) or a treatment which receives an identical intervention as TECH plus a study designed team competition for physical activity promotion (TECH+COMP).
研究类型
介入性
注册 (实际的)
116
阶段
- 不适用
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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South Carolina
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Columbia、South Carolina、美国、29208
- University of South Carolina
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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 65年 (成人、年长者)
接受健康志愿者
是的
有资格学习的性别
全部
描述
Inclusion Criteria:
- Insufficiently active as determined by a one-week, accelerometer-based physical activity measurement
- Body mass index (BMI) between 25 kg/m2 and 55 kg/m2
- Between ages 18 and 65 years
- Access to computer with Internet connection
- Smartphone ownership (Android or iOS)
- Willing to be randomized to either one of the two study groups
- Part of a self-selected team of 3-8 eligible individuals
- Members of the same household cannot be part of separate groups
- Able to walk at least 1/4 mile without stopping
Exclusion Criteria:
- Currently lactating, pregnant, or planning to become pregnant during the length of the study
- Diagnosed with type 1 or type 2 diabetes
- Medical or physical contraindications or limitations for engaging in physical activity
- History of major medical or psychiatric conditions
- Currently participating in a physical activity program
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：治疗
- 分配：随机化
- 介入模型：并行分配
- 屏蔽：无（打开标签）
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
有源比较器：TECH (Technology)
Participants will receive a theory-based physical activity program.
They will enroll in the study as part of a self-selected group of 3-8 individuals.
They will be provided with a personal step goal and Fitbit Alta HR for self-monitoring physical activity.
They will also have access to a study website that will be accessible across conventional and mobile platforms.
They will be asked to visit the website each week to receive behavior change information and guidance.
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Participants will receive a theory-based physical activity program. They will enroll in the study as part of a self-selected group of 3-8 individuals. They will be provided with a personal step goal and Fitbit Alta HR for self-monitoring physical activity. They will also have access to a study website that will be accessible across conventional and mobile platforms. They will be asked to visit the website each week to receive behavior change information and guidance. Device: Fitbit Alta HR |
|
实验性的：TECH+COMP (Technology + Competition)
Participants will receive the same intervention components as the TECH goup, as well as a study designed team competition.
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Participants will receive the same intervention components as the TECH group, as well as a team competition. The competition will be based on the following two aspects: total daily steps accumulated relative to group size and total number of points retained for achieving weekly physical activity challenges. Device: Fitbit Alta HR |
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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Accelerometer-measured change from Baseline Daily Steps at 3 months and 12 months
大体时间：0, 3, and 12 months
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Change in daily steps
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0, 3, and 12 months
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Accelerometer-measured change from Baseline Minutes of Moderate-to-Vigorous Physical Activity at 3 months and 12 months
大体时间：0, 3, and 12 months
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Change in moderate-to-vigorous physical activity
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0, 3, and 12 months
|
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Change from Baseline in Perceived Social Support for Exercise (Sallis Social Support and Exercise Survey) at 3 and 12 months
大体时间：0, 3, and 12 months
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Change in perceived social support for exercise (scale total score range: 1 to 5, with 1 representing low perceived social support for exercise and 5 representing high perceived social support for exercise; responses to all items are averaged to yield a total final score)
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0, 3, and 12 months
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其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Participant Satisfaction (Satisfaction Questionnaire)
大体时间：4 months
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Participant satisfaction with treatment
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4 months
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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。
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)
2018年4月30日
初级完成 (预期的)
2019年1月1日
研究完成 (预期的)
2019年5月1日
研究注册日期
首次提交
2018年4月16日
首先提交符合 QC 标准的
2018年4月16日
首次发布 (实际的)
2018年4月26日
研究记录更新
最后更新发布 (实际的)
2018年11月28日
上次提交的符合 QC 标准的更新
2018年11月27日
最后验证
2018年4月1日
更多信息
与本研究相关的术语
其他研究编号
- 2018
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)？
不
IPD 计划说明
Data will only be reported in aggregate.
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.
TECH (Technology)的临床试验
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University of Campania Luigi VanvitelliDentsply Sirona Implants and Consumables完全的
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Dentsply Sirona Implants and Consumables完全的
-
Dentsply Sirona Implants and Consumables完全的