Actively Recruiting
Reliability, Validity, and Responsiveness of the Turkish Version of Eating Assessment Tool-10 for Patients With Primer Sjögren's Syndrome
Led by Kahramanmaras Sutcu Imam University · Updated on 2024-06-25
100
Participants Needed
1
Research Sites
25 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Reliability, Validity, and Responsiveness of the Turkish Version of Eating Assessment Tool-10 for Patients With Primer Sjögren's Syndrome
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients diagnosed with Primary Sj�f6gren's Syndrome
- 18 years or older
You will not qualify if you...
- Patients with Secondary Sj�f6gren's Syndrome
- Patients diagnosed with other uncontrolled or clinically important diseases such as chronic obstructive pulmonary disease, congestive heart failure, endocrine system diseases, neurological or psychological diseases
- Individuals who do not agree to participate in the study and do not give written consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hacettepe University
Ankara, Turkey (Türkiye)
Actively Recruiting
Research Team
N
Nazli Elif Nacar, MSc
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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