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Clinical Trials/NCT00741650
NCT00741650
Completed
Phase 2

Ibedrift- Health Related Coping. A Randomized Controlled Trial Comparing a Worksite Educational Intervention With or Without Referral to Treatment as Usual.

NORCE Norwegian Research Centre AS1 site in 1 country2,097 target enrollmentSeptember 2008

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Neck Pain Musculoskeletal
Sponsor
NORCE Norwegian Research Centre AS
Enrollment
2097
Locations
1
Primary Endpoint
Sick Leave
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

A randomized controlled trial comparing a new approach to musculoskeletal pain consisting of education and peer involvement to treatment as usual. All local government employees in 1-3 Norwegian municipalities will be invited to participate.

Detailed Description

The purpose of the study is to systematically test a new treatment method for musculoskeletal pain in Norway. The intervention focuses on attempting to treat musculoskeletal pain outside the traditional medical system as much as possible, to avoid the establishment of a patient identity and passive patient behavior. In addition, participants are given reasons to stay active, and not advice to stay active. Ibedrift is a randomized controlled trial with the aim of studying the effect of a new treatment regime for musculoskeletal pain, focusing on didactic information about low back pain with peer support. Those participants not in the control group will have the option of contacting a peer advisor, a non health professional trained by the iBedrift crew to give information about back pain and reasons to stay active. For those who have not recovered within a short period of time, and who are randomized to full treatment, the peer advisor can send them directly to health personnel for a brief intervention consisting of a medical examination with screening for conditions that need treatment, counseling and education. The intervention was done in 2 Norwegian municipalities for all local government employees. Randomization was done at the level of working units (schools, offices etc) which allows for more message containment.

Registry
clinicaltrials.gov
Start Date
September 2008
End Date
December 2012
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • All employees above 18 years

Exclusion Criteria

  • Known congenital musculoskeletal disease
  • Cauda equina syndrome

Outcomes

Primary Outcomes

Sick Leave

Time Frame: 1 year and 2 year after start of intervention

Secondary Outcomes

  • Low Back pain(1 year and 2 years after intervention)
  • Subjective Health complaints(1 year and 2 years after intervention)

Study Sites (1)

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