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Clinical Trials/NCT02047669
NCT02047669
Completed
Not Applicable

Implementation of Physical Exercise at the Workplace (IRMA09) - Laboratory Technicians

National Research Centre for the Working Environment, Denmark1 site in 1 country112 target enrollmentMarch 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Musculoskeletal Disorders
Sponsor
National Research Centre for the Working Environment, Denmark
Enrollment
112
Locations
1
Primary Endpoint
Pain intensity
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

Musculoskeletal disorders and stress of employees remain a major problem in many occupations. The aim of this study is to investigate the effect of an individually tailored bio-psycho-social intervention strategy versus "usual care" ergonomics and standard physical exercises (reference group) on musculoskeletal pain, work disability, and stress in lab technicians with a history of work-related musculoskeletal pain.

Registry
clinicaltrials.gov
Start Date
March 2014
End Date
July 2014
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
National Research Centre for the Working Environment, Denmark
Responsible Party
Principal Investigator
Principal Investigator

Lars L. Andersen

Professor, PhD

National Research Centre for the Working Environment, Denmark

Eligibility Criteria

Inclusion Criteria

  • Laboratory technician
  • Pain intensity \>= 3 (scale of 0-10)
  • Pain duration \>= 3 months
  • Pain frequency \>= 3 days per week

Exclusion Criteria

  • life threatening disease
  • pregnancy

Outcomes

Primary Outcomes

Pain intensity

Time Frame: change from baseline to week 10

The change in "pain intensity during the last week" (average value of back, neck, shoulder, elbow and hand) from baseline to 10 week follow-up between the individually tailored biopsychosocial group and reference group. 2-way analysis of variance with repeated measures will be used, with time, group and time x group as fixed factors and subject as random factor. Analyses will be controlled for pain intensity at baseline.

Secondary Outcomes

  • Stress(change from baseline to week 10)

Study Sites (1)

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