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Clinical Trials/NCT02541890
NCT02541890
Completed
Not Applicable

Effects of Workplace Intervention in Inpatient Occupational Rehabilitation on Return to Work for Persons With Somatic and/or Common Mental Health Problems. A Randomised Controlled Trial

Norwegian University of Science and Technology1 site in 1 country175 target enrollmentApril 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Mental Disorders
Sponsor
Norwegian University of Science and Technology
Enrollment
175
Locations
1
Primary Endpoint
Time until sustainable return to work
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Aim is to study the effect of a work place intervention during a multicomponent return-to-work rehabilitation program on return-to-work. The intervention is compared with inpatient rehabilitation only, and participants will be recruited from the diagnostic groups dominating the sick-leave statistics, namely musculoskeletal disorders, common mental disorders (e.g. stress, depression and anxiety), and unspecific disorders including chronic fatigue.

Detailed Description

Long-term sick-listing from work has considerable impact on social function, on the families of the sick-listed persons, the companies they work for, and society as a whole. Hence, the need for documented effective vocational rehabilitation programs is pressing. Vocational rehabilitation services described in the scientific literature have been specific to one single or a specific group of medical conditions (e.g.low back pain). In contrast, most people on sick leave have several health complaints, and many of the factors influencing sick leave are shared regardless of disorder (e.g. social surroundings, workplace environment), calling for rehabilitation programs that can be employed for both musculoskeletal, unspecific and common mental disorders. Research indicates that interventions on the work place might facilitate return to work. The aim of this study is therefore to investigate the effect of a work place intervention during a multicomponent return-to-work rehabilitation program on return-to-work.

Registry
clinicaltrials.gov
Start Date
April 2015
End Date
March 2018
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Resident of Central Norway
  • Sick-listed due to common mental disorders, musculoskeletal pain/problems, unspecific disorders and/or fatigue
  • Sick-listed more than 50 %
  • Sick-listed longer than 8 weeks
  • Has employer and is willing to participate in a work place intervention during the rehabilitation program

Exclusion Criteria

  • is self-employed
  • has, or is currently examined for, a serious somatic or psychiatric disorder
  • suffers from substance abuse
  • has trouble with participating in a group
  • is in a rehabilitation process that will interfere with the occupational rehabilitation program
  • function level is to weak to participate in the rehabilitation program

Outcomes

Primary Outcomes

Time until sustainable return to work

Time Frame: 12 months

Register data from the national health and welfare services

Number of days on sick-leave

Time Frame: 12 months

Register data from the national health and welfare services

Secondary Outcomes

  • Pain. Questionnaire(12 months)
  • Health related quality of life. Questionnaire(12 months)
  • Psychological flexibility and acceptance. Questionnaire(5 months)
  • Well-being at work. Single question(5 months)
  • Use of health services. Questionnaire. "How much of this health/social service have you used during the last 4 months?"(12 months)
  • Expectations about sick leave and return to work. Questionnaire(5 months)
  • Fear and avoidance beliefs about work. Questionnaire(5 months)
  • Return to work self efficacy. Questionnaire.(5 months)
  • Readiness for return to work. Questionnaire(5 months)
  • Work ability. Single question(5 months)

Study Sites (1)

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