This study follows people with axial spondyloarthritis to understand how delays in diagnosis affect their health outcomes and quality of life. Researchers will collect real-world data from patients across Britain to learn more about this inflammatory spine condition.
Key Objective: The study aims to identify how earlier diagnosis of axial spondyloarthritis can improve patient outcomes and guide better treatment strategies.
Who to Consider: People recently diagnosed with axial spondyloarthritis or those with early symptoms of this condition should consider enrolling to contribute to understanding this disease.
Trial Parameters
Brief Summary
The British Axial Spondyloarthritis Cohort (BAxSIC) study has been established under the auspices of the British Society for Spondyloarthritis (BRITSpA) in collaboration with the National Axial Spondyloarthritis Society (NASS) to provide real-world data to evaluate the impact of delay in diagnosis (from symptom onset to diagnosis) on work participation and functional outcomes and the natural history and impact of newly-diagnosed axial Spondyloarthritis, including disease activity, pain, fatigue, functional and work outcomes, comorbidities, therapies in the United Kingdom (UK). The study is a prospective cohort, enrolling patients attending rheumatology clinics in the UK who are newly diagnosed with axial Spondyloarthritis and naïve to biologic therapy. The study will run for an initial 3 year period commencing January 2023. Financial support was provided as a Research Grant from Pfizer Limited, UCB and Novartis.
Eligibility Criteria
Inclusion Criteria: 1. Aged ≥16 years. 2. A physician diagnosis of axSpA (including ankylosing spondylitis) within the last 6 months prior to baseline. 3. Willing and able to give informed consent to participate in the study. Exclusion Criteria: 1. Age \<16 years. 2. Unable to communicate in English or are deemed, in any other way, to be unable to give informed consent