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

NCT06230952 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 102

Last updated 2024-05-29

No results posted yet for this study

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.

Conditions

  • Axial Spondyloarthritis

Interventions

OTHER

BASDAI and BASFI reliability

The study will be carried out on volunteer patients who are diagnosed with axial spondyloarthritis and are followed up in the outpatient clinic of Dokuz Eylül University, Department of Internal Medicine, Rheumatology and Immunology Department, and who meet the inclusion criteria. Patients who volunteer to participate in the study will be contacted by phone and BASDAI and BASFI questionaires will be administered.

Sponsors & Collaborators

  • Siirt University

    lead OTHER

Principal Investigators

  • Yasemin ACAR, PhD · Siirt University

Eligibility

Min Age
20 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-02-08
Primary Completion
2024-05-27
Completion
2024-05-27

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06230952 on ClinicalTrials.gov