Efficacy of a Combined Ergonomic Health Promotion Intervention on Employee Health
研究概览
地位
详细说明
Primary Aim: To compare the effects of providing sedentary employees with seated active workstations in combination with an ergonomic intervention and regular motivational emails (experimental group) against the ergonomic intervention and regular emails only (active control group) on occupational sedentary behavior over 16 weeks.
Hypothesis: The addition of a seated active workstation will result in significant reductions in daily occupational sedentary time compared to the active control group.
Secondary Aims: To compare the effects of the experimental group against the active control group on secondary measures of cardiometabolic disease risk factors, musculoskeletal discomfort, cognitive function and work productivity.
Hypothesis 1: The experimental group will result in reduced cardiometabolic disease risk, musculoskeletal discomfort and work limitations compared to the active control group.
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
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Iowa
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Iowa City、Iowa、美国、52242
- University of Iowa
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- We will recruit overweight/obese (body mass index 25.0-40.0 kg/m2) adults (18-65 years) working in full-time (minimum 35 hours/week), sedentary (self-report sitting >75% work time) occupations at an independent work site.
Exclusion Criteria:
- Working in an office that will not meet the space or electrical requirements of the active workstation, acute or chronic illness not under treatment of a provider, orthopedic limitations that prohibit physical activity, current or planned pregnancy, hospitalization from a physical or mental disorder in the past six months and/or taking medication that may impair physical activity
学习计划
研究是如何设计的?
设计细节
- 主要用途:预防
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
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实验性的:Experimental Group
This group will receive the seated active workstation intervention, the ergonomic intervention and the email intervention for 16 weeks.
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Participants in the experimental group will receive a seated active workstation at their work setting for 16 weeks.
Participants of both arms will receive a face to face ergonomic workstation optimization intervention.
This consultation will take 30 minutes to complete and will be performed at the participant's actual work station.
Participants of both arms will receive three emails per week for 16 weeks.
Messages will be consistent with what they hear in the ergonomic intervention (e.g., encourage taking breaks from sitting at work and adjusting posture to be in line with ergonomic principles).
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有源比较器:Active Control
This group will receive the ergonomic intervention and email intervention only for 16 weeks.
This group will not receive a seated active workstation.
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Participants of both arms will receive a face to face ergonomic workstation optimization intervention.
This consultation will take 30 minutes to complete and will be performed at the participant's actual work station.
Participants of both arms will receive three emails per week for 16 weeks.
Messages will be consistent with what they hear in the ergonomic intervention (e.g., encourage taking breaks from sitting at work and adjusting posture to be in line with ergonomic principles).
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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 Occupational Physical Activity From Baseline to 16 Weeks
大体时间:Baseline and 16 weeks
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Occupational physical activity (primary outcome) will be measured objectively with the GENEActiv physical activity monitor.
The monitor will be worn on the right ankle and will be worn for 5 working days during all non-bathing hours.
The outcome measure will be change in occupational activity (average counts/work day) from baseline to 16 weeks.
The measure will be calculated as follows: 16 weeks value - baseline value.
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Baseline and 16 weeks
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合作者和调查者
出版物和有用的链接
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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.
Active Workstation Intervention的临床试验
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Sophiahemmet UniversityKarolinska Institutet; Linnaeus University; The Swedish School of Sport and Health Sciences; Stockholm... 和其他合作者尚未招聘
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University of Illinois at ChicagoShirley Ryan AbilityLab; Oakland University; Access Living主动,不招人
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University of Wisconsin, MadisonNational Cancer Institute (NCI); Northwestern University主动,不招人