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Resistance Exercise to Improve Fatigue in Workplace (REW) (REW)

2019年4月16日 更新者:Rosimeire Simprini Padula

Effectiveness of a Resistance Training Program in the Workplace to Muscle Fatigue Control in Industrial Workers: Cluster Randomized Controlled Trial.

Studies show that exercise resistance in workplace can reduce the symptoms of induced labor, however, the effectiveness of such programs depends on the characteristics of the training fatigue. Thus, it is expected that this study the intervention group with training heavy using progressive resistance exercise protocol will be better in reducing fatigue when compare with light training group.

研究概览

详细说明

Background: This study is randomized clinical trial with double-blinded. The aim is evaluate the effectiveness the training heavy with resistance exercise program in the muscle fatigue control. Methods: This is a randomized controlled trial by cluster, in which workers who participate in the intervention group will perform resistance exercise protocols; and workers in the comparative group held only stretching exercises and light resistance training with elastic bands. Expected results: strong evidence that fatigue reducing after ten weeks in workers and improve in others outcomes. Not found in literature studies in occupational evaluating this aspect of training.

研究类型

介入性

注册 (实际的)

352

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

    • Espirito Santo
      • Cachoeiro de Itapemirim、Espirito Santo、巴西、29303300
        • Centro Universitário São Camilo

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:

  • sign informed consent

Exclusion Criteria:

  • restriction by the medical department.

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:随机化
  • 介入模型:并行分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
有源比较器:Compensatory Workplace Exercise (CWE)
Comparative Group will receive a light training protocol including warming up, stretching and resisted exercise using elastic bands.
The comparative group will receive warming up and stretching and light resisted exercise with elastic bands. The exercise will realize three times per week, 20 minutes for day in total 60 minutes per week. With warming up for 5 minutes and 15 minutes of the specific training . The exercise will realize in 3 series with 10 repetitions and rest 30 seconds between series.
实验性的:Individual Resistance Exercise (IRE)
Intervention group will receive training protocol including warming up, stretching a specific resistance training with increase progressive load.
Intervention group will receive warming up and stretching, and a specific resistance training with increase progress load. The exercise will realize three times per week, 20 minutes for day in total 60 minutes per week. With warming up and stretching for 5 minutes and 15 minutes of the specific training. The exercise will realize in 3 series with 10 repetitions and rest 30 seconds between series.

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
Need for Recovery
大体时间:up to 4 months
Psychosocial risk factors and stress, resulting in work-induced fatigue, will be obtained by e Need for Recovery Scale (NFR).
up to 4 months
Fatigue
大体时间:up to 4 months
1 RM test is the maximum amount of weight lifted once while performing a standardized exercise for muscle groups - elbow , knee and ankle flexors and extensors, trunk. A weight according to the maximum capacity is chosen. If a replay is completed, find the value of 1RM.
up to 4 months

次要结果测量

结果测量
措施说明
大体时间
Musculoskeletal symptoms
大体时间:Outcome measures will be assessed at baseline and after 4 months.
Musculoskeletal symptoms (pain, tingling or numbness) will be assessed using the Nordic Questionnaire for Musculoskeletal.
Outcome measures will be assessed at baseline and after 4 months.
Level of physical activity
大体时间:Outcome measures will be assessed at baseline and after 4 months.
Questionnaire Baeck will be used to identify the level of habitual physical activity
Outcome measures will be assessed at baseline and after 4 months.
Perceived exposure
大体时间:Outcome measures will be assessed at baseline and after 4 months.
The perception of workers risk factors that may contribute to the development of musculoskeletal complaints will be evaluated through the Job Factors Questionnaire.
Outcome measures will be assessed at baseline and after 4 months.
Physical Fitness Assessment
大体时间:Outcome measures will be assessed at baseline and after 4 months.
The physical assessment will be consider adipometry (body fat percentage) others variables.
Outcome measures will be assessed at baseline and after 4 months.
Productivity
大体时间:Outcome measures will be assessed at baseline and after 4 months.
Productivity is measured by a single item General Health Questionnaire and Performance at Work
Outcome measures will be assessed at baseline and after 4 months.

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:Rosimeire S Padula、Universidade Cidade de Sao Paulo

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)

2015年10月20日

初级完成 (实际的)

2016年12月12日

研究完成 (实际的)

2017年3月3日

研究注册日期

首次提交

2014年6月19日

首先提交符合 QC 标准的

2014年6月23日

首次发布 (估计)

2014年6月24日

研究记录更新

最后更新发布 (实际的)

2019年4月17日

上次提交的符合 QC 标准的更新

2019年4月16日

最后验证

2019年4月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • 454.709

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.

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