Evaluating the impact of fibromyalgia on patients in Poland
Assessment of Functioning and Disability of People With Fibrimyalgia in Poland
University of Rzeszow · NCT06296446
This study is trying to understand how fibromyalgia affects daily life for people in Poland by using an online survey to gather information about their pain, emotions, and sleep.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 700 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Rzeszow (other) |
| Locations | 1 site (Rzeszów, Podkarpacie) |
| Trial ID | NCT06296446 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess the functioning and disability of individuals suffering from fibromyalgia in Poland. It will utilize an online survey to gather data on various factors affecting patients, including pain intensity, emotional state, and sleep quality. The study will employ established assessment tools such as the WHODAS 2.0 and Fibromyalgia Impact Questionnaire (FIQ) to evaluate the level of disability. The findings will contribute to a better understanding of how fibromyalgia affects daily life and functioning in this population.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and over who have been diagnosed with fibromyalgia.
Not a fit: Patients who are underage or do not have a diagnosis of fibromyalgia will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the challenges faced by fibromyalgia patients, potentially leading to improved care and support strategies.
How similar studies have performed: While there is limited research on this topic in Poland, similar studies in other countries have successfully evaluated the impact of fibromyalgia on functioning and disability.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * People aged 18 and over * People suffering from fibromyalgia * People who give informed consent to participate in the study Exclusion Criteria: Tłumaczenie * Underage persons * People without fibromyalgia * People who do not give informed consent to participate in the study
Where this trial is running
Rzeszów, Podkarpacie
- University of Rzeszow — Rzeszów, Podkarpacie, Poland (RECRUITING)
Study contacts
- Principal investigator: Agnieszka Sozańska — University of Rzeszow
- Study coordinator: Agnieszka Sozańska, prof.
- Email: asozanska@ur.edu.pl
- Phone: +48 530172857
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.
Conditions: Fibromyalgia, Disabilities Multiple, fibromyalgia, disability evaluation, functioning, WHODAS 2.0, FIQ, BDI