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

S

Siirt University

Status

Completed

Conditions

Axial Spondyloarthritis

Treatments

Other: BASDAI and BASFI reliability

Study type

Observational

Funder types

Other

Identifiers

NCT06230952
2023/39-19

Details and patient eligibility

About

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

Full description

Telehealth is the provision of healthcare services and clinical practices remotely through information and communication technologies. In recent years, the use of telehealth applications has increased worldwide. Telehealth is an umbrella term that covers practices such as telemedicine, telerehabilitation, and tele-assessment. Tele-assessment has gained importance in terms of monitoring patients with chronic diseases. Although BASDAI and BASFI have been shown to be valid and reliable in AS patients, there is no study in the literature examining the reliability of BASDAI and BASFI applied via tele-assessment. The aim of our study is to investigate the reliability of BASDAI and BASFI questionnaires administered via tele-assessment in axial SpA patients.

Enrollment

102 patients

Sex

All

Ages

20 to 60 years old

Volunteers

No Healthy Volunteers

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

Trial design

102 participants in 1 patient group

axial spondyloarthritis patients
Description:
patients diagnosed with axial spondyloarthritis
Treatment:
Other: BASDAI and BASFI reliability

Trial contacts and locations

1

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Central trial contact

Yasemin ACAR, PhD

Data sourced from clinicaltrials.gov

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