Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT06299917

WORK-ON Vocational Rehabilitation for People with Inflammatory Arthritis

Led by The Danish Center for Expertise in Rheumatology · Updated on 2024-10-09

56

Participants Needed

1

Research Sites

182 weeks

Total Duration

On this page

Sponsors

T

The Danish Center for Expertise in Rheumatology

Lead Sponsor

O

Odense Patient Data Explorative Network

Collaborating Sponsor

AI-Summary

What this Trial Is About

People with chronic inflammatory arthritis (IA) (rheumatoid arthritis, axial spondyloarthritis, and psoriatic arthritis), often have a reduced work ability. Up to 40% lose their job in the first years after diagnosis. Consequently, they are at high risk of losing their jobs and being permanently excluded from the labour market. Therefore, a new context-specific vocational rehabilitation (VR) for people with IA was developed, based on the Medical Research Council's framework for complex interventions. The 6-months VR is called WORK-ON and consists of three parts: 1) a coordinating occupational therapist who performs an initial assessment and goalsetting process and supports cooperation between relevant partners and navigation between sectors, 2) Four group sessions with peers and if needed, 3) Individual sessions with a social worker, nurse, or physiotherapist. The objective of the WORK-ON trial is to test the overall efficacy on work ability compared to a control group who receives usual care and pamphlets for their employer and colleagues. Based on the experiences from a feasibility study, WORK-ON will be conducted as a randomised controlled trial. Patients with IA, aged 18 years or older, experiencing job insecurity will be randomised to one of two groups: the WORK-ON VR group or usual care (control group). The primary outcome; work ability measured is measured by Work Ability Index single item, at baseline, 6, 12, 18 and 30 months after baseline. Secondary outcomes are absenteeism, presenteeism, overall work impairment, activity impairment, job loss, quality of life, mental well-being, fatigue, sleep, physical activity, occupational balance and pain. Secondary outcomes are measured at baseline, 6 and 12 months after baseline. In addition, work ability, working hours per week and job loss are measured at 18 and 30 months after baseline.

CONDITIONS

Official Title

WORK-ON Vocational Rehabilitation for People with Inflammatory Arthritis

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18-65 years.
  • Diagnosed with rheumatoid arthritis, psoriatic arthritis, or axial spondyloarthritis by a rheumatologist.
  • Currently undertakes paid work or studying (full- or part-time).
  • Able to read and understand Danish.
  • Answers 'unlikely' or 'not certain' to the question: 'Do you believe, according to your present state of health, that you will be able to do your current job two years from now?'
  • Willing to participate in a randomized controlled trial of the WORK-ON vocational rehabilitation program.
Not Eligible

You will not qualify if you...

  • Planned or recent changes to anti-rheumatic medication within the last three months.
  • Other medical conditions besides inflammatory arthritis that may reduce work ability.
  • Under examination for other medical conditions affecting work ability.
  • Major surgery within the past six months or planned surgery.
  • Unable to understand or speak Danish sufficiently.
  • Cognitive or psychological impairments affecting participation.
  • Planned or ongoing participation in another rehabilitation program (except physiotherapy).
  • Previously participated in the WORK-ON feasibility study.
  • Retirement application in process or plans to retire within five years.
  • Taken long-term sick leave of more than four weeks.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Danish Hospital for Rheumatic Diseases

Sønderborg, Denmark, 6400

Actively Recruiting

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Research Team

C

Christina M T Madsen, MSc

CONTACT

J

Jette Primdahl, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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