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Work Place Adjusted Intelligent Physical Exercise Reducing Musculoskeletal Pain in Shoulder and Neck

Work Place Adjusted Intelligent Physical Exercise Reducing Musculoskeletal Pain in Shoulder and Neck (VIMS, Danish Acronym)

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01027390
Acronym
VIMS
Enrollment
573
Registered
2009-12-08
Start date
2010-01-31
Completion date
2011-02-28
Last updated
2012-12-11

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

Conditions

Musculoskeletal Disorders

Keywords

neck/shoulder

Brief summary

Musculoskeletal disorders are frequent among office workers especially in the neck/shoulder area. The hypothesis is, that specific strength training of the neck/shoulder muscles will alleviate the pain. The two sub-hypotheses are 1. Alleviation of pain is independent of training frequency 2. Alleviation of pain is higher following supervised training vs training with initial instruction only

Detailed description

Recent studies have shown a positive effect of work site physical exercise intervention, however, there is a lack of evidence regarding: 1) extend of instruction and supervision, and 2) frequency of training session during the wek. Questionnaires will be send to around 2000 office workers inviting them to participate in work site training for 1 hr per week for 20 weeks. Those accepting the invitation will be randomized into 5 different groups: 1. training 1 hr one time per week supervized 50% of the time 2. training 3 x 20 min per week supervised 50 % of the time 3. training 3 x 20 min per week supervised only initially with careful instructions 4. training 10 x 6 min per week supervised 50 % of the time 5. no training serving as reference control group At termination of the training period there will be a follow-up questionnaire survey

Interventions

BEHAVIORALphysical training exercise

physical exercise training at the work site during work time

Sponsors

National Research Centre for the Working Environment, Denmark
CollaboratorOTHER_GOV
University of Copenhagen
CollaboratorOTHER
University of Southern Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* office workers * employed

Exclusion criteria

* physically heavy work * trauma * leif threatening disease, e.g. cancer, * pregnancy

Design outcomes

Primary

MeasureTime frame
neck/shoulder pain, selfreported20 weeks

Secondary

MeasureTime frame
muscle strength and endurance20 weeks

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 31, 2026