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Completed

NCT Number: NCT02541890

Effects of Workplace Intervention in Occupational Rehabilitation on Return to Work

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.

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Nowegian University of Science and Technology, Department of public health

Trondheim, 7491, Norway

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Work place intervention

Behavioral

Meeting at the work place including the patient, the employer and the rehabilitation therapist. Aim of meeting is to discuss challenges and possibilities in the patient's return to work process and to make a plan for return to work.

Primary outcomes

  1. Number of days on sick-leave

    Time frame: 12 months

    Register data from the national health and welfare services

  2. Time until sustainable return to work

    Time frame: 12 months

    Register data from the national health and welfare services

Secondary outcomes

  1. Use of health services. Questionnaire. "How much of this health/social service have you used during the last 4 months?"

    Time frame: 12 months

    160 participants. "How much of this health/social service have you used during the last 4 months?" Somatic and mental health specialized care (in-patient and outpatient), general practitioner, psychologist, group therapy, physiotherapist, chiropractor, occupational rehabilitation, welfare services, complementary practitioner, emergency unit, ambulatory services, occupational health services, other treatment.

  2. Pain. Questionnaire

    Time frame: 12 months

    Brief pain inventory (BPI). 160 participants

  3. Health related quality of life. Questionnaire

    Time frame: 12 months

    The 15D health-related quality of life instrument. 160 participants

  4. Psychological flexibility and acceptance. Questionnaire

    Time frame: 5 months

    Acceptance and action questionnaire and work acceptance and action questionnaire (AAQ2). 160 participants

  5. Return to work self efficacy. Questionnaire.

    Time frame: 5 months

    Return to work self-efficacy-19 (RTWSE-19). 160 participants.

  6. Fear and avoidance beliefs about work. Questionnaire

    Time frame: 5 months

    Fear Avoidance Belief Questionnaire (FABQ). 160 participants

  7. Expectations about sick leave and return to work. Questionnaire

    Time frame: 5 months

    160 participants. "How long do you anticipate to be sick-listed (partly/fully)?" 3 questions.

  8. Work ability. Single question

    Time frame: 5 months

    160 participants. "How will you rate your work ability?" (scale from 0 (no ability) to 10 (my best ability)).

  9. Well-being at work. Single question

    Time frame: 5 months

    160 participants. "How happy are you at work?" (not at all, not so good, good. very good)

  10. Readiness for return to work. Questionnaire

    Time frame: 5 months

    160 participants. Readiness for return to work (RRTW) questionnaire.

Sponsors and collaborators

Lead sponsor

Norwegian University of Science and Technology

Other

Collaborators

  • Trondheim University Hospital

Registry information

Official study title

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

Important dates

Study start
2015
Primary completion
2017
Study completion
2018
First posted
Sep 4, 2015
Registry last updated
Aug 13, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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