Skip to main content
Clinical Trials/ISRCTN45748422
ISRCTN45748422
Completed
未知

Evaluating the Effectiveness of Motivational Interviewing in Injured Workers with Musculoskeletal Disorders: A Cluster Randomized Controlled Trial

Workers' Compensation Board of Alberta0 sites200 target enrollmentFebruary 12, 2015

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Workers' Compensation Board of Alberta
Enrollment
200
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

2017 Results article in https://doi.org/10.1016/j.apmr.2017.06.003 (added 08/03/2023) 2017 Results article in https://doi.org/10.1007/s10926-017-9712-3 (added 08/03/2023)

Registry
who.int
Start Date
February 12, 2015
End Date
December 1, 2016
Last Updated
3 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Workers' Compensation Board of Alberta

Eligibility Criteria

Inclusion Criteria

  • Workers’ compensation claimants with musculoskeletal injuries being treated at Millard Health Centre in Edmonton, Canada. Specific inclusion criteria for this study consist of the following:
  • 1\. Injured workers 18 years and older who have an open WCB\-Alberta claim
  • 2\. Off work 3 to 12 months post injury
  • 3\. Not job attached or have experienced an unsuccessful gradual RTW
  • 4\. Participating in a provider\-based RTW program with integrated vocational services
  • 5\. Not scheduled for surgery
  • 6\. No major psychological or psychiatric diagnosis (including severe depression, psychosis, brain injury or traumatic psychological injury)

Exclusion Criteria

  • 1\. Injured workers less than 18 years old who have an open WCB\-Alberta claim
  • 2\. Off work more than 12 months post injury
  • 3\. Have a job to return to
  • 4\. Not participating in a provider\-based RTW program with integrated vocational services
  • 5\. Scheduled for surgery
  • 6\. Major psychological or psychiatric diagnosis (including severe depression, psychosis, brain injury or traumatic psychological injury)

Outcomes

Primary Outcomes

Not specified

Similar Trials