Actively Recruiting
Orthorexia Nervosa in Postmenopausal Osteoporosis
Led by Beylikduzu State Hospital · Updated on 2025-04-27
128
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
A total of 64 female patients diagnosed with osteoporosis based on dual-energy X-ray absorptiometry (DXA) measurements performed within the last six months, and 64 age-matched healthy controls without osteoporosis, will be included in our study. Sociodemographic data such as age, sex, height, weight, and BMI will be recorded. Additionally, information regarding the duration of osteoporosis diagnosis, current treatments, history of fractures, history of falls, comorbidities, and smoking status will be collected. Femoral neck and L1-L4 T-scores and bone mineral density values obtained from existing DXA scans will be documented. Orthorexia nervosa-related symptoms will be assessed using the ORTO-11 scale, mood will be evaluated using the Hospital Anxiety and Depression Scale (HADS), and body image will be assessed using the Body Appreciation Scale-2.
CONDITIONS
Official Title
Orthorexia Nervosa in Postmenopausal Osteoporosis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women between 55-75 years
- Women diagnosed with osteoporosis based on DXA measurements performed within the past six months
- Women aged similarly to the osteoporosis group without a diagnosis of osteoporosis (healthy controls)
- Willingness to participate and provision of written informed consent
You will not qualify if you...
- Refusal to participate in the study
- Diagnosed psychiatric disorders
- Cognitive impairment
- Presence of malignancy
- Presence of endocrine disorders (e.g., hyperthyroidism, Cushing's syndrome)
- Use of glucocorticoids
- Use of medications affecting mood
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Beylikdüzü State Hospital
Istanbul, Turkey (Türkiye), 34147
Actively Recruiting
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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