Study in Ankylosing Spondylitis (AS) and Psoriatic Arthritis (PsA) Patients to Evaluate Work Productivity Before and After the Start of Adalimumab Therapy in Daily Practice in Belgium

Study Identifier
P13-990
CT.gov Identifier
NCT01845818
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact

844-663-3742 or [email protected]

Study Complete

Results Available

Protocol
Available Language(s): English
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Statistical Analysis Plan
Available Language(s): English
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Scientific Result Summary
Available Language(s): English
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Study Details

Medical Condition
  • Axial Spondyloarthritis (axSpA)
  • Psoriatic Arthritis (PsA)
    • Study Drug
    N/A
    Phase
    N/A
    Sex
    Female & Male
    Age
    18 - 50 Years
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    * Patient \>= 18 years and \<= 50 years * Patient diagnosed with AS or PsA * Patient to be initiated on adalimumab (according to the Marketing Authorization and Belgian reimbursement criteria) * Patient willing to sign informed consent
    Exclusion Criteria:
    * Any contraindication for adalimumab as specified in the corresponding Summary of Product Characteristics (SmPC) * Patient previously treated with biologics * Patient participating in other AbbVie-sponsored trials

    Protocol Summary

    This observational study will document to what extent in daily clinical practice the work productivity is affected before and after the start of adalimumab treatment.

    Changes in the employment status and work productivity of participants with AS and PsA before and after the start of adalimumab will be noted. The relationship between employment status, work productivity, disease activity and clinical evaluations will be evaluated. Since AS and PsA might be diseases with a strong impact on the daily life of the participant, an evaluation will be performed to the effect of the disease on quality of life and work productivity.

    Study Locations

    No locations found.