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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02498197
Other study ID # IRMA11
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 2016
Est. completion date December 2017

Study information

Verified date August 2018
Source National Research Centre for the Working Environment, Denmark
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

There is high prevalence of back pain and neck-shoulder pain among blue collar workers. Physical excessive exposures such as heavy lifting or working with a bended or twisted back are independent risk factors for back pain among workers in the construction industry. Participatory ergonomic initiatives increase the success of interventions aimed at reducing physical excessive exposures.

The objectives are in two phases to; 1) determine which work-tasks in selected job-groups involve the highest load of the back and shoulders during a normal working day (using EMG, Actigraphs, Video). 2) investigate whether a participatory intervention can reduce physical workloads, drawing on information from objective measurements from phase 1.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date December 2017
Est. primary completion date June 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 67 Years
Eligibility Inclusion Criteria:

- Full time construction workers who are member of a labor union and can read and understand Danish.

- The type of work must include manual work that involves lifting

Exclusion Criteria:

- life-threatening diseases

- pregnancy

- hypertension >160/100 mmHg

- unable to participate in the measurements

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Participatory Intervention

Control


Locations

Country Name City State
Denmark National Research Centre for the Working Environment Copenhagen

Sponsors (2)

Lead Sponsor Collaborator
National Research Centre for the Working Environment, Denmark Aalborg University

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Other Social Capital questionnaire Social Capital within work teams, between work teams, and between teams and their leaders Reference for questionnaire: http://www.ncbi.nlm.nih.gov/pubmed/26261190 change from baseline to 3 months follow-up
Primary Excessive physical load The primary outcome of the present study is the change from baseline to follow-up in frequency of events with excessive physical load change from baseline to 3 months follow-up
Secondary Pain intensity (0-10) Change in "low back pain intensity during the last week" from baseline to follow-up. A horizontally oriented modified VAS scale will be used with 11 points from 0 to 10. change from baseline to 3 months follow-up
Secondary WAI questionnaire Work Ability Index (Ilmarinen et al) change from baseline to 3 months follow-up
Secondary Self-efficacy Questionnaire Self-efficacy to improve the physical work environment change from baseline to 3 months follow-up
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