Work Injury Prevention in Law Enforcement Officials
2015年7月1日 更新者：University of the Pacific
Effectiveness of an Exercise-based Work Injury Prevention Program in Law Enforcement Officials
Law enforcement officials (LEOs) demonstrate an elevated risk for occupational injury.
The effectiveness of exercise-based work injury prevention programs (WIPPs) to reduce the risk and costs associated with occupational injury has yet to be tested rigorously in LEOs.
The accuracy of existing field tests of physical functioning to predict occupational injuries and related expenses remains unclear.
The objectives of this study are to: (i) determine the effect of an exercise-based WIPP on occupational wellness and productivity in a cohort of LEOs, and (ii) to determine the accuracy of 2 common field assessments of physical function to predict lost work productivity and related expenses in a cohort of LEOs.
研究概览
研究类型
介入性
注册 (预期的)
108
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
-
-
California
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Chico、California、美国、95928
- Butte Premier Physical Therapy
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Davis、California、美国、95618
- Physical Edge
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Lodi、California、美国、95240
- PUMP Institute
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Lodi、California、美国、95242
- Lodi Physical Therapy
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Stockton、California、美国、95211
- University of the Pacific
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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 60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:
- Age between 18 and 60 years
- Working full duty as a law enforcement official
Exclusion Criteria:
- Current history of pathology or symptoms that preclude exercise
- Medical or rehabilitative treatment for a work-related injury within the past year prior to enrollment in this study
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：Exercise
Exercise will occur 3 times weekly for 6 months in 20-minute exercise sessions.
Sessions will take place independently.
Follow-up and progression of the home program will be completed in person or by video teleconferencing at regular intervals throughout the intervention phase.
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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 |
|---|---|---|
|
Number of Work Injury Claims During the Study Period
大体时间：One time, at one year following enrollment into the study
|
One time, at one year following enrollment into the study
|
|
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Medical Expenditures Related to Work Injury Claims During the Study Period
大体时间：One time, at one year following enrollment into the study
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One time, at one year following enrollment into the study
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|
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Number of Missed Work Days Due to Illness or Injury
大体时间：One time, at one year following enrollment into the study
|
One time, at one year following enrollment into the study
|
|
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Work Productivity and Activity Impairment Questionnaire - General Health Subscale
大体时间：Weekly, up to one year following enrollment into the study
|
The Work Productivity and Activity Impairment (WPAI) Questionnaire was developed to measure the personal and economic effects of lost workplace productivity in the context of clinical trials.
In this study, the WPAI-General Health (GH) version will be used in order to assess lost productivity and wellness during the study period.
The WPAI-GH is a 6-item scale that solicits the number of hours missed from work and level of functional impairment perceived at work during the previous week.
Four scores are calculated from the WPAI-GH, including percentage of work time missed due to health, percentage impairment while working due to health, percentage activity impairment due to health, an overall percentage work impairment.
Time series data will be collected to observe trends over time that may relate to independent variables in this study, as well as to examine for previously unknown and uncontrolled variation (ie, seasonal variability).
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Weekly, up to one year following enrollment into the study
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Functional Movement Screen
大体时间：One time, at 3 months following enrollment into the study
|
The purpose of the Functional Movement Screen (FMS) is to provide the clinician with a rapid triage for potentially problematic regions that can contribute to symptoms, disablement, or injury.
As a triage tool, FMS is used to determine regions that require additional clinical investigation.
The FMS is a battery of 7 tests that are intended as an integrated assessment for limitations in range of motion, weakness, and incoordination.
FMS tests consider spine, upper extremity, and lower extremity movements in the context of their respective regional kinetic chain.
Component tests of the FMS involve rating of performance by a standardized examiner on a 3-point scale, and specific criteria exist for each rating.
A composite score for the FMS may be calculated by summing the item scores.
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One time, at 3 months following enrollment into the study
|
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Star Balance Excursion Test
大体时间：One time, at 3 months following enrollment into the study
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The Star Excursion Balance Test is a clinical test of dynamic balance.
Subjects will assume unilateral stance in the center of a grid marked circumferentially in 45-degree increments.
After a learning trial consisting of 6 repetitions in each of the 8 test directions, subjects will complete 3 repetitions of single limb squat reach.
The evaluating therapist will record the distance achieved between the stance toe and heel of the reaching extremity in each of 3 repetitions in each direction.
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One time, at 3 months following enrollment into the study
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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
2012年8月1日
初级完成 (预期的)
2015年12月1日
研究完成 (预期的)
2015年12月1日
研究注册日期
首次提交
2012年8月3日
首先提交符合 QC 标准的
2013年6月11日
首次发布 (估计)
2013年6月14日
研究记录更新
最后更新发布 (估计)
2015年7月2日
上次提交的符合 QC 标准的更新
2015年7月1日
最后验证
2015年7月1日
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.