Rheumatoid Arthritis Clinical Trial
Official title:
Time to DMARD Treatment and Actual Work Limitation of Patients With Rheumatoid Arthritis in Turkey
The objective is to measure time delay from onset of symptoms to diagnosis and time to disease-modifying anti-rheumatic drug treatments in Turkish patients with rheumatoid arthritis. The investigators will also evaluate actual work limitation status of patients and impact of demographic and clinical factors on work limitations in rheumatoid arthritis patients.
This post marketing observational study will be conducted in cross-sectional,
non-interventional, multi-center format in Turkey. As this is a post marketing observational
study, Abbott is not involved in the product supply since the drug is being used according
to the approved marketing label and is to be prescribed by the physician under usual and
customary practice of physician prescription.
Subjects will be recruited from rheumatology outpatient clinics of university hospitals
and/or private offices.
Patients diagnosed with rheumatoid arthritis who had received at least one disease-modifying
anti-rheumatic drug, who are already employed at a paid work and able to provide disease
history data will be included.
Patient data will be collected with a single visit. During the single visit, all required
demographic and clinical data will be recorded on the case report forms by the investigators
and every subject will be asked to fill out the Work Productivity and Activity Impairment
questionnaire and the Health Assessment Questionnaire - Disability Index.
;
Time Perspective: Cross-Sectional
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