Examining Orthorexia Nervosa in Women with Fibromyalgia
Is There a Link Between Orthorexia Nervosa, Body Image and Psychological State in Women With Fibromyalgia Syndrome?
This study is trying to see how symptoms of orthorexia nervosa relate to pain and overall well-being in women with fibromyalgia.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 84 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | Female |
| Sponsor | Beylikduzu State Hospital Academic / other |
| Locations | 1 site (Istanbul) |
| Trial ID | NCT06947200 on ClinicalTrials.gov |
What this trial studies
This observational study will include 84 female patients aged 18 to 65 diagnosed with fibromyalgia according to established criteria. It aims to assess various factors including pain severity, orthorexia nervosa symptoms, body image, mood, and the overall impact of fibromyalgia on the patients' lives. Data will be collected through validated scales such as the Visual Analog Scale (VAS), ORTO-11 scale, Body Appreciation Scale 2, Hospital Anxiety and Depression Scale (HADS), and the Fibromyalgia Impact Questionnaire (FIQ). The study will provide insights into the relationship between orthorexia nervosa and fibromyalgia.
Who should consider this trial
Good fit: Ideal candidates are female patients aged 18-65 with a diagnosis of fibromyalgia.
Not a fit: Patients with diagnosed psychiatric disorders or cognitive impairments may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding of the psychological aspects of fibromyalgia, potentially leading to improved treatment strategies.
How similar studies have performed: While studies on fibromyalgia are common, the specific focus on orthorexia nervosa in this context is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Female patients aged 18-65 years. * Diagnosis of fibromyalgia syndrome according to the 2010 American College of Rheumatology diagnostic criteria. * Willingness to participate and provision of written informed consent. Exclusion Criteria: * Refusal to participate. * Presence of diagnosed psychiatric disorders. * Presence of cognitive impairment. * Use of medications that may affect mood.
Where this trial is running
Istanbul
- Beylikdüzü State Hospital — Istanbul, Turkey (Türkiye) (Recruiting)
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.