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Completed

NCT Number: NCT02047682

Implementation of Physical Exercise at the Workplace (IRMA10) - Occupational Load

Static postures, repetitive work tasks, and work stress increase the risk for musculoskeletal disorders and sickness absence. Objective measurements of occupational loadings - EMG for muscular activity, EEG for cognitive activity, ECG for cardiovascular activity and heart rate variability, actigraphy for bodily movements - may provide useful early indicators of muscular, cognitive and cardiovascular overload.

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 these risk factors in lab technicians with a history of work-related musculoskeletal pain.

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Key information

Age range

18 year–67 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

National Research Centre for the Working Environment

Copenhagen, 2100, Denmark

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Biopsychosocial

Behavioral

Reference

Behavioral

Primary outcomes

  1. EMG gaps

    Time frame: change from baseline to week 10

    Electromyography (EMG) is measured in the neck and shoulder muscles throughout a normal workday before and after the intervention. EMG gaps is defined as periods with muscular inactivity. Actigraphs are used to measure bodily movements, and only period with sitting or standing work are included in the analysis (i.e. walking activities are excluded from the analyses)

Secondary outcomes

  1. EEG

    Time frame: change from baseline to week 10

    Electroencephalography is measured throughout a normal workday before and after the intervention. Actigraphs are used to measure bodily movements, and only period with sitting or standing work are included in the analysis (i.e. walking activities are excluded from the analyses)

  2. HRV

    Time frame: change from baseline til 10 week followup

    Heart Rate Variability (HRV) is measured with Actiheart throughout the working day before and after the intervention. Actigraphs are used to measure bodily movements, and only period with sitting or standing work are included in the analysis (i.e. walking activities are excluded from the analyses)

Sponsors and collaborators

Lead sponsor

National Research Centre for the Working Environment, Denmark

Other Gov

Collaborators

  • University of Southampton

Registry information

Acronym: IRMA10

Important dates

Study start
2014
Primary completion
2014
Study completion
2014
First posted
Jan 28, 2014
Registry last updated
Sep 30, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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