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OpenTrials
Completed

NCT Number: NCT01921764

Implementation of Physical Exercise at the Workplace (IRMA08) - Healthcare Workers

The prevalence and consequences of musculoskeletal pain is considerable among healthcare workers, allegedly due to high physical work demands of healthcare work. Previous studies have shown promising results of physical exercise for relieving pain among different occupational groups, but the question remains whether such physical exercise should be performed at the workplace or in the private sphere at home. Performing physical exercise at the workplace together with colleagues may be more motivating for some employees and thus increase compliance. On the other hand, physical exercise at the workplace may be costly for the employers in terms of time spend. Thus, relevant ground exists to compare the efficacy of workplace- versus home-based training on musculoskeletal pain. This study investigates the effect of workplace-based versus home-based physical exercise on musculoskeletal pain among healthcare workers.

The main hypothesis is that physical exercise at the workplace for 10 weeks compared with physical exercise at home results in reduced musculoskeletal pain among healthcare workers.

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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

  • healthcare worker
  • female
  • age 18-67

Exclusion criteria

  • life threatening disease
  • pregnancy

Treatment and study plan

Workplace physical exercise

Behavioral

Home physical exercise

Behavioral

Primary outcomes

  1. Pain intensity

    Time frame: change from baseline to week 10

    The change in "pain intensity during the last week" from baseline to 10 week follow-up between the workplace- and home-training group. The home-training group will be considered the reference group. 2-way analysis of variance (Proc Mixed of SAS) with repeated measures will be used, with time and group as fixed factors and subject as random factor. Department will be added as a cluster effect.

Secondary outcomes

  1. Muscle function

    Time frame: change from baseline to week 10

  2. Work ability index (WAI)

    Time frame: change from baseline to week 10

  3. Physical exertion during work

    Time frame: change from baseline to week 10

Sponsors and collaborators

Lead sponsor

National Research Centre for the Working Environment, Denmark

Other Gov

Registry information

Acronym: IRMA

Important dates

Study start
2013
Primary completion
2013
Study completion
2014
First posted
Aug 13, 2013
Registry last updated
Jan 28, 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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