Reliability, Validity, and Responsiveness of the Turkish Version of Eating Assessment Tool-10 for Patients With Primer Sjögren's Syndrome

Last updated: June 24, 2024
Sponsor: Kahramanmaras Sutcu Imam University
Overall Status: Active - Recruiting

Phase

N/A

Condition

Sjogren's Syndrome

Dermatomyositis (Connective Tissue Disease)

Treatment

N/A

Clinical Study ID

NCT06401811
KSU.
  • Ages > 18
  • All Genders

Study Summary

Evaluations will be made by researchers following the guidance of individuals with primary Sjögren's Syndrome who receive diagnosis, routine medical care, and treatment management.

In addition, for the reliability of the Turkish Eating Assessment Tool-10, the Turkish Eating Assessment Tool-10 will be repeated on patients at least one-fifth of the number of individuals included, after one week.

For the sensitivity of the scale, an exercise that is routinely applied in the Rheumatological Rehabilitation Unit of Hacettepe University Faculty of Physical Therapy and Rehabilitation will be invited and after 3 months, the same evaluations as applied in the first measurement will be made again on individuals at least one-fifth of the number of individuals included.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients diagnosed with Primary Sjögren's Syndrome

  • 18 years or older

Exclusion

Exclusion Criteria:

  • Patients with Secondary Sjögren's Syndrome,

  • Patients who are diagnosed with other uncontrolled/clinically important diseases (chronic obstructive pulmonary disease, congestive heart failure, endocrine systemdiseases, neurological, psychological diseases, etc.),

  • Individuals who do not agree to participate in the study and do not give writtenconsent will be excluded from the study.

Study Design

Total Participants: 100
Study Start date:
June 04, 2024
Estimated Completion Date:
November 30, 2024

Connect with a study center

  • Hacettepe University

    Ankara,
    Turkey

    Active - Recruiting

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