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Work Place Adjusted Intelligent Physical Exercise Reducing Musculoskeletal Pain in Shoulder and Neck (VIMS) - Industrial Workers (VIMS)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01071980
Recruitment Status : Completed
First Posted : February 19, 2010
Last Update Posted : October 11, 2012
Sponsor:
Collaborators:
University of Copenhagen
University of Southern Denmark
Information provided by (Responsible Party):
Lars L. Andersen, National Research Centre for the Working Environment, Denmark

Brief Summary:
The purpose of this study is to investigate the effect of specific resistance training on neck/shoulder pain in industrial workers.

Condition or disease Intervention/treatment Phase
Non-specific Pain of the Neck and Shoulder Other: Work Place Adjusted Intelligent Physical Exercise Reducing Musculoskeletal Pain in Shoulder and Neck Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 522 participants
Allocation: Randomized
Intervention Model: Factorial Assignment
Masking: Single (Investigator)
Primary Purpose: Prevention
Official Title: Work Place Adjusted Intelligent Physical Exercise Reducing Musculoskeletal Pain in Shoulder and Neck (VIMS) - Industrial Workers
Study Start Date : January 2009
Actual Primary Completion Date : February 2010
Actual Study Completion Date : February 2010

Arm Intervention/treatment
Active Comparator: Specific resistance training
3 x 20 min a week of specific resistance training for 20 weeks
Other: Work Place Adjusted Intelligent Physical Exercise Reducing Musculoskeletal Pain in Shoulder and Neck
Participants will be randomized at the cluster level to a control group or 20 weeks of specific resistance training for 3 x 20 min a week

No Intervention: Control
Control group



Primary Outcome Measures :
  1. Pain of the neck and shoulders [ Time Frame: At week 0 (baseline) and week 20 (follow-up) ]
  2. Pain in the arm/hand [ Time Frame: At week 0 (baseline) and week 20 (follow-up) ]


Information from the National Library of Medicine

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Ages Eligible for Study:   20 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • industrial worker

Exclusion Criteria:

  • trauma, life threatening diseases, pregnancy

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01071980


Locations
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Denmark
National Research Centre for the Working Environment
Copenhagen, Denmark, 2100
Sponsors and Collaborators
National Research Centre for the Working Environment, Denmark
University of Copenhagen
University of Southern Denmark
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

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Responsible Party: Lars L. Andersen, Senior Researcher, PhD, National Research Centre for the Working Environment, Denmark
ClinicalTrials.gov Identifier: NCT01071980    
Other Study ID Numbers: VIMS00
First Posted: February 19, 2010    Key Record Dates
Last Update Posted: October 11, 2012
Last Verified: October 2012
Additional relevant MeSH terms:
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Musculoskeletal Pain
Shoulder Pain
Muscular Diseases
Musculoskeletal Diseases
Pain
Neurologic Manifestations
Arthralgia
Joint Diseases