Short-term Behavior Change With Pedal Desk Installation (PD-ST)
2019年3月28日 更新者:Corby K. Martin、Pennington Biomedical Research Center
The purpose of this investigation is to evaluate participant use of a dedicated office pedal desk with and without behavioral support.
研究概览
地位
终止
详细说明
For this pilot study the investigators will identify and recruit up to 20 full time Pennington Biomedical staff members employed in sedentary jobs (i.e., report mostly sitting during working hours).
The sample size is limited by the number of pedal desks being built for this pilot study and the need for timely data generation.
Although the investigators can stagger starts as needed, all participants must intend to be on campus for the subsequent 6 weeks after they start the intervention.
Two cohorts of 10 participants will complete the three 2-week conditions in the following order: 1) SELF-DIRECTED use where participants have access to their daily recorded data but will not have any other form of feedback or goal-setting; 2) FACILITATED use where participants are provided with their daily recorded pedal desk data and additional daily behavioral support from an interventionist (e.g., feedback and goal-setting) to increase their use of the pedal desk by an individually negotiated and agreed upon amount; 3) FACILITATED use with PEDOMETER where participants will be provided with their daily recorded pedal desk and step count data and additional daily behavioral support from an interventionist (e.g., feedback and goal-setting) to increase their use of the pedal desk by an individually negotiated and agreed upon amount and increase their step count by 3,000 steps/day compared to baseline.
Participants will be asked to pedal at a sustainable and self-selected pace while using the pedal desk.
研究类型
介入性
注册 (实际的)
7
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
-
-
Louisiana
-
Baton Rouge、Louisiana、美国、70808
- Pennington Biomedical Research Center
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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
21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:
- Be a full-time employee at Pennington Biomedical Research Center
- Be between 21 and 65 years of age
- Primarily sit while at work
- Work from a private office/cubicle
Exclusion Criteria:
- Weigh more than 250 pounds
- Have physical limitations that prevent performance of pedaling motions
- Plan to be away from work for the 6 weeks of the intervention
- Be pregnant
- Have a pace maker and/or metal joint replacement
- Plan to be away from work for the 6 weeks of the intervention
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:其他
- 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 |
---|---|
其他:Pedal Desk
Participants will complete three 2-week conditions in the following order:
|
participants will have a pedal desk installed in their office and will have access to their daily recorded data but will not have any other form of feedback or goal-setting
participants are provided with their daily recorded pedal desk data and additional daily behavioral support from an interventionist (e.g., feedback and goal-setting) to increase their use of the pedal desk by an individually negotiated and agreed upon amount
participants will be provided with their daily recorded pedal desk and step count data and additional daily behavioral support from an interventionist (e.g., feedback and goal-setting) to increase their use of the pedal desk by an individually negotiated and agreed upon amount and increase their step count by 3,000 steps/day compared to baseline.
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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 |
---|---|---|
Weight Change (kg)
大体时间:Baseline to 6 weeks
|
KG weight change from Baseline to 6 weeks
|
Baseline to 6 weeks
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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:Corby K Martin, PhD、Pennington Biomedical Research Center
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
2014年5月1日
初级完成 (实际的)
2015年7月1日
研究完成 (实际的)
2015年7月1日
研究注册日期
首次提交
2014年3月12日
首先提交符合 QC 标准的
2014年4月4日
首次发布 (估计)
2014年4月9日
研究记录更新
最后更新发布 (实际的)
2019年3月29日
上次提交的符合 QC 标准的更新
2019年3月28日
最后验证
2019年3月1日
更多信息
与本研究相关的术语
关键字
其他研究编号
- PBRC 2013-051
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
未定
IPD 计划说明
Yes
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.