Resistance Exercise to Improve Fatigue in Workplace (REW) (REW)
Primary Purpose
Fatigue, Musculoskeletal Diseases
Status
Completed
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Compensatory Workplace Exercise (CWE) - Comparative Group
Individual Resistance Exercise (IRE) - Intervention Group
Sponsored by
About this trial
This is an interventional prevention trial for Fatigue focused on measuring Workplace, Industrial workers, Resistance exercise, Fatigue, Occupational risk, Physical therapy
Eligibility Criteria
Inclusion Criteria:
- sign informed consent
Exclusion Criteria:
- restriction by the medical department.
Sites / Locations
- Centro Universitário São Camilo
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Compensatory Workplace Exercise (CWE)
Individual Resistance Exercise (IRE)
Arm Description
Comparative Group will receive a light training protocol including warming up, stretching and resisted exercise using elastic bands.
Intervention group will receive training protocol including warming up, stretching a specific resistance training with increase progressive load.
Outcomes
Primary Outcome Measures
Need for Recovery
Psychosocial risk factors and stress, resulting in work-induced fatigue, will be obtained by e Need for Recovery Scale (NFR).
Fatigue
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.
Secondary Outcome Measures
Musculoskeletal symptoms
Musculoskeletal symptoms (pain, tingling or numbness) will be assessed using the Nordic Questionnaire for Musculoskeletal.
Level of physical activity
Questionnaire Baeck will be used to identify the level of habitual physical activity
Perceived exposure
The perception of workers risk factors that may contribute to the development of musculoskeletal complaints will be evaluated through the Job Factors Questionnaire.
Physical Fitness Assessment
The physical assessment will be consider adipometry (body fat percentage) others variables.
Productivity
Productivity is measured by a single item General Health Questionnaire and Performance at Work
Full Information
NCT ID
NCT02172053
First Posted
June 19, 2014
Last Updated
April 16, 2019
Sponsor
Rosimeire Simprini Padula
1. Study Identification
Unique Protocol Identification Number
NCT02172053
Brief Title
Resistance Exercise to Improve Fatigue in Workplace (REW)
Acronym
REW
Official Title
Effectiveness of a Resistance Training Program in the Workplace to Muscle Fatigue Control in Industrial Workers: Cluster Randomized Controlled Trial.
Study Type
Interventional
2. Study Status
Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
October 20, 2015 (Actual)
Primary Completion Date
December 12, 2016 (Actual)
Study Completion Date
March 3, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Rosimeire Simprini Padula
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
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.
Detailed Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fatigue, Musculoskeletal Diseases
Keywords
Workplace, Industrial workers, Resistance exercise, Fatigue, Occupational risk, Physical therapy
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
352 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Compensatory Workplace Exercise (CWE)
Arm Type
Active Comparator
Arm Description
Comparative Group will receive a light training protocol including warming up, stretching and resisted exercise using elastic bands.
Arm Title
Individual Resistance Exercise (IRE)
Arm Type
Experimental
Arm Description
Intervention group will receive training protocol including warming up, stretching a specific resistance training with increase progressive load.
Intervention Type
Other
Intervention Name(s)
Compensatory Workplace Exercise (CWE) - Comparative Group
Intervention Description
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.
Intervention Type
Other
Intervention Name(s)
Individual Resistance Exercise (IRE) - Intervention Group
Intervention Description
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.
Primary Outcome Measure Information:
Title
Need for Recovery
Description
Psychosocial risk factors and stress, resulting in work-induced fatigue, will be obtained by e Need for Recovery Scale (NFR).
Time Frame
up to 4 months
Title
Fatigue
Description
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.
Time Frame
up to 4 months
Secondary Outcome Measure Information:
Title
Musculoskeletal symptoms
Description
Musculoskeletal symptoms (pain, tingling or numbness) will be assessed using the Nordic Questionnaire for Musculoskeletal.
Time Frame
Outcome measures will be assessed at baseline and after 4 months.
Title
Level of physical activity
Description
Questionnaire Baeck will be used to identify the level of habitual physical activity
Time Frame
Outcome measures will be assessed at baseline and after 4 months.
Title
Perceived exposure
Description
The perception of workers risk factors that may contribute to the development of musculoskeletal complaints will be evaluated through the Job Factors Questionnaire.
Time Frame
Outcome measures will be assessed at baseline and after 4 months.
Title
Physical Fitness Assessment
Description
The physical assessment will be consider adipometry (body fat percentage) others variables.
Time Frame
Outcome measures will be assessed at baseline and after 4 months.
Title
Productivity
Description
Productivity is measured by a single item General Health Questionnaire and Performance at Work
Time Frame
Outcome measures will be assessed at baseline and after 4 months.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
sign informed consent
Exclusion Criteria:
restriction by the medical department.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rosimeire S Padula
Organizational Affiliation
Universidade Cidade de São Paulo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centro Universitário São Camilo
City
Cachoeiro de Itapemirim
State/Province
Espirito Santo
ZIP/Postal Code
29303300
Country
Brazil
12. IPD Sharing Statement
Citations:
PubMed Identifier
32493267
Citation
Santos HG, Chiavegato LD, Valentim DP, Padula RS. Effectiveness of a progressive resistance exercise program for industrial workers during breaks on perceived fatigue control: a cluster randomized controlled trial. BMC Public Health. 2020 Jun 3;20(1):849. doi: 10.1186/s12889-020-08994-x.
Results Reference
derived
PubMed Identifier
28003034
Citation
Santos HG, Chiavegato LD, Valentim DP, da Silva PR, Padula RS. Resistance training program for fatigue management in the workplace: exercise protocol in a cluster randomized controlled trial. BMC Public Health. 2016 Dec 22;16(1):1218. doi: 10.1186/s12889-016-3872-5.
Results Reference
derived
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Resistance Exercise to Improve Fatigue in Workplace (REW)
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