Evaluating a new questionnaire for myositis patients
Investigation of the Validity, Reliability, and Responsiveness of the BETY-Biopsychosocial Questionnaire in Individuals Diagnosed with Myositis
This study is testing a new questionnaire to see how well it helps understand the physical and emotional challenges faced by people with myositis.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Hacettepe University Academic / other |
| Locations | 1 site (Ankara, Altındağ) |
| Trial ID | NCT06587724 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess the validity, reliability, and responsiveness of the BETY-Biopsychosocial Questionnaire (BETY-BQ) in individuals diagnosed with myositis. The study focuses on understanding how myositis affects physical function, quality of life, and psychosocial factors such as anxiety and depression. By utilizing a comprehensive questionnaire, the research seeks to provide insights into the holistic evaluation of patients and improve disease management. Participants will be asked to complete the BETY-BQ to gather data on their experiences and challenges related to myositis.
Who should consider this trial
Good fit: Ideal candidates for this study are adults over 18 years old who have been diagnosed with myositis.
Not a fit: Patients with uncontrolled or clinically significant diseases, pregnant individuals, or those with malignancies may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved assessment tools that enhance the management and treatment of myositis patients.
How similar studies have performed: While the approach of using a biopsychosocial questionnaire is innovative, similar studies have shown promise in improving patient assessments in related conditions.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Diagnosis of myositis * To be over 18 years old * Consent of the participant Exclusion Criteria: * Uncontrolled/other clinically significant disease (chronic obstructive pulmonary disease, congestive heart failure, endocrine system diseases, neurological, psychological diseases, etc.) individuals with a diagnosis, * Pregnant individuals, * Individuals with malignancy
Where this trial is running
Ankara, Altındağ
- Hacettepe University — Ankara, Altındağ, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: Orkun Tüfekçi, PT, PhD (c)
- Email: orkuntf@gmail.com
- Phone: 5319502648
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.