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Clinical Trials/NCT00791596
NCT00791596
Completed
Phase 4

Effectiveness of an Ergonomic Intervention on Work-Related Posture and Low Back Pain in Video Display Terminal Operators: a 3 Year Cross-Over Trial

University of Bologna1 site in 1 country200 target enrollmentJanuary 2005

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Low Back Pain
Sponsor
University of Bologna
Enrollment
200
Locations
1
Primary Endpoint
R.E.B.A. (Rapid Entire Body Assessment) method
Status
Completed
Last Updated
17 years ago

Overview

Brief Summary

This Research study aims to investigate the long term effectiveness of a workstation ergonomic intervention for work-related posture and low back pain (LBP) of Video Display Terminal (VDT) workers

Detailed Description

A non-randomized, crossover trial design was used with follow-up repeated 6, 12, and 30 months from baseline in the first intervention period and then beginning at 6 months following the crossover. The administrative offices in the two main buildings of the town hall of Forlì, Italy. The study population was composed of 400 employees, who used VDTs for at least 20 hours a week, of whom we randomly selected 100 participants from each building. Of the 200 initial participants, 153 completed the study; the dropouts were due to illness/injury or maternity. Participants were assigned to intervention or control during the first period and then crossed over after a 30-month washout. The intervention used in this investigation was an ergonomic adjustment of the VDT workstation design. Our study showed that the workstation ergonomic adjustment improved work-related posture and in reducing LBP in VDT operators among subjects who received the intervention both in the first period and in the crossover, and maintained these positive effects for at least 30 months.

Registry
clinicaltrials.gov
Start Date
January 2005
End Date
December 2007
Last Updated
17 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
University of Bologna

Eligibility Criteria

Inclusion Criteria

  • The study population was composed of 400 employees, who used VDTs for at least 20 hours a week

Exclusion Criteria

  • Subjects were excluded if pregnant or had a medical history of serious injury, spinal surgery, malignant pathology, or severe disability

Outcomes

Primary Outcomes

R.E.B.A. (Rapid Entire Body Assessment) method

Time Frame: Baseline, 6 months, 12 months, 30 months, 36 months

Secondary Outcomes

  • Pain Drawing with a Visual Analogue Scale(Baseline, 6 months, 12 months, 30 months, 36 months)

Study Sites (1)

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