CompletedNot Applicable

Reliability of BASDAI and BASFI Applied by Tele-Assessment Method in Axial SpA Spondyloarthritis

Turkey (Türkiye)102 participantsStarted 2024-02-08

Plain-language summary

The goal of this observational study is to investigate the reliability of BASDAI and BASFI questionnaires applied via tele-assessment in axial spondyloarthritis patients.

Who can participate

Age range20 Years – 60 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Being diagnosed with Axial spondyloarthritis according to the Assessment in SpondyloArthritis international Society (ASAS) criteria * Volunteering to participate in the study * Being between the ages of 20-60 Exclusion Criteria: * Having another systemic, orthopedic, neurological or cognitive disease other than axial spondyloarthritis * Pregnancy * The patient wishes to withdraw from the study

What they're measuring

Bath Ankylosing Spondylitis Disease Activity Index (BASDAI)

Timeframe: Baseline and after 24 hours after baseline assessment

Bath Ankylosing Spondylitis Functional Index (BASFI)

Timeframe: Baseline and after 24 hours after baseline assessment

Trial details

NCT IDNCT06230952

SponsorSiirt University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2024-05-27

View on ClinicalTrials.gov More Axial Spondyloarthritis trials