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Implementation of Physical Exercise at the Workplace (IRMA06) - Slaughterhouse Workers

Implementation of Physical Exercise at the Workplace (IRMA06) - Slaughterhouse Workers

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01671267
Acronym
IRMA
Enrollment
66
Registered
2012-08-23
Start date
2012-08-31
Completion date
2013-02-28
Last updated
2014-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Musculoskeletal Disorders

Brief summary

The prevalence of pain in the shoulder, arm and hand is high among slaughterhouse workers, allegedly due to the substantial load of these body regions during work. Work disability is a common consequence of these pains. Lowering the physical exposure through ergonomic intervention may be a strategy to reduce the workload. An alternative strategy could be to increase the physical capacity through strength training of the shoulder-, arm- and hand-muscles. This study investigates the effect of two contrasting interventions, i.e. load reduction (ergonomic intervention) versus training of physical capacity (strength training) on pain and work disability in slaughterhouse workers. The main hypothesis is that strength training intervention for 10 weeks compared with ergonomic intervention results in reduced pain of the shoulder, arm and hand.

Interventions

BEHAVIORALStrength training
BEHAVIORALErgonomic

Sponsors

National Research Centre for the Working Environment, Denmark
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 67 Years
Healthy volunteers
Yes

Inclusion criteria

* Slaughterhouse worker * the pain should have lasted at least 3 months * pain intensity during the last three months of \>= 3 (scale 0-10) in the shoulder, elbow or hand * the pain should be frequent (at least 3 days per week)

Exclusion criteria

* life threatening disease * pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Pain intensitychange from baseline to week 10The change in pain intensity during the last week (average value of shoulder, elbow and hand) from baseline to 10 week follow-up between the strength training group and ergonomic group. The ergonomic 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.

Secondary

MeasureTime frameDescription
DASHchange from baseline to week 10Disability of the arm, shoulder and hand questionnaire (DASH). Only the work-module of DASH will be included. Analyzed the same way as the primary outcome.

Other

MeasureTime frameDescription
PPTchange from baseline to week 10Pressure pain threshold of the muscle of the forearm, external rotators of the shoulder, and tibialis anterior of the leg (reference muscle).
WAIchange from baseline to week 10Work ability index questionnaire
Total tenderness scorechange from baseline to week 10change in examiner-verified tenderness of the muscles of the shoulder, arm and hand. Scale of no, a little, moderate and severe tenderness. Summed up to a total tenderness score (Andersen LL 2011, PMID: 21177034)

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026