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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01027390
Other study ID # H-C-2008-103
Secondary ID
Status Completed
Phase Phase 0
First received December 7, 2009
Last updated December 8, 2012
Start date January 2010
Est. completion date February 2011

Study information

Verified date December 2012
Source University of Southern Denmark
Contact n/a
Is FDA regulated No
Health authority Denmark: The Danish National Committee on Biomedical Research Ethics
Study type Interventional

Clinical Trial 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


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


Other known NCT identifiers
  • NCT01056068

Recruitment information / eligibility

Status Completed
Enrollment 573
Est. completion date February 2011
Est. primary completion date January 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- office workers

- employed

Exclusion Criteria:

- physically heavy work

- trauma

- leif threatening disease, e.g. cancer,

- pregnancy

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Prevention


Intervention

Behavioral:
physical training exercise
physical exercise training at the work site during work time

Locations

Country Name City State
Denmark Rigspolitiet Copenhagen

Sponsors (3)

Lead Sponsor Collaborator
University of Southern Denmark National Research Centre for the Working Environment, Denmark, University of Copenhagen

Country where clinical trial is conducted

Denmark, 

References & Publications (2)

Andersen CH, Andersen LL, Gram B, Pedersen MT, Mortensen OS, Zebis MK, Sjøgaard G. Influence of frequency and duration of strength training for effective management of neck and shoulder pain: a randomised controlled trial. Br J Sports Med. 2012 Nov;46(14) — View Citation

Andersen LL, Zebis MK, Pedersen MT, Roessler KK, Andersen CH, Pedersen MM, Feveile H, Mortensen OS, Sjøgaard G. Protocol for work place adjusted intelligent physical exercise reducing musculoskeletal pain in shoulder and neck (VIMS): a cluster randomized — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary neck/shoulder pain, selfreported 20 weeks No
Secondary muscle strength and endurance 20 weeks No
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