WORK-ON Vocational Rehabilitation for People with Inflammatory Arthritis

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorThe Danish Center for Expertise in Rheumatology

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Aged 18-65 years.

Diagnosed with RA, PsA or axSpA by a rheumatologist.

Undertakes paid work (full- or part-time work or studying).

Able to read and understand Danish.

Disqualifiers

Planned or present adjustments of the pharmacological anti-rheumatic treatment (DMARDs, glucocorticoid) within the last three months.

Presence of morbidities other than IA that may explain reduced work ability.

Is under examination for comorbidities that influence work ability.

Major surgery was conducted within the past six months, or a surgery has been planned.

Trial design

Design model

Parallel

Treatments tested in this trial

  • WORK-ON

    Other intervention

    The intervention includes three parts: 1) a coordinating occupational therapist, 2) four group sessions and 3) Individual consultations based on the agreed upon goals.

Treatment groups

56 Participants
are divided into 2 treatment groups
Group A: WORK-ONExperimental treatment 1 intervention
Group B: Usual careNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Work Ability Index (WAI) single item

A visual analogue scale that compares perceived work ability with lifetime best score. The score ranges from 0 (completely unable to work) to 10 (work ability at its best)

Time frame
Baseline to 6 months after baseline

Secondary outcomes

1

Job loss

Number of participants who currently has a job

Time frame
6,12,18 and 30 months after baseline
2

Work hours per week

Number of work hours per week

Time frame
Baseline, 6,12,18 and 30 months after baseline
3

Work Productivity and Activity Impairment questionnaire, general health (WPAI:GH)

Measures Absenteeism, Presenteeism, Overall work impairment and Activity impairment.

Time frame
Baseline, 6,12,18 and 30 months after baseline
4

Sickness absenteeism

Days and hours of sick leave

Time frame
Each month after baseline during the 6 month intervention period via text message reminders.

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

The Danish Center for Expertise in Rheumatology

Lead sponsor

University of Southern Denmark

Sponsor institution

Odense Patient Data Explorative Network

Collaborator

The Danish Rheumatism Association

Collaborator

Danish Association of Occupational Therapist

Collaborator

Schaufuss foundation

Collaborator