Orthorexia Nervosa in Fibromyalgia

NCT ID: NCT06947200

Last Updated: 2025-04-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

84 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-04-20

Study Completion Date

2025-05-20

Brief Summary

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This clinical cross-sectional study will include 84 female patients aged between 18 and 65 years who have been diagnosed with fibromyalgia syndrome according to the 2010 American College of Rheumatology diagnostic criteria. Sociodemographic data will be recorded at the beginning of the study. Pain severity will be assessed using the Visual Analog Scale (VAS). Orthorexia nervosa-related symptoms will be evaluated with the ORTO-11 scale. Body image will be assessed with the Body Appreciation Scale 2, mood will be evaluated using the Hospital Anxiety and Depression Scale (HADS), and fibromyalgia-related impact will be assessed with the Fibromyalgia Impact Questionnaire (FIQ).

Detailed Description

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Conditions

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Fibromyalgia

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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fibromyalgia group

Fibromyalgia

Intervention Type OTHER

no intervention

Interventions

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Fibromyalgia

no intervention

Intervention Type OTHER

Other Intervention Names

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No intervention

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Beylikduzu State Hospital

OTHER

Sponsor Role lead

Responsible Party

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Busra Sirin

Principle Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Beylikdüzü State Hospital

Istanbul, , Turkey (Türkiye)

Site Status RECRUITING

Countries

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Turkey (Türkiye)

Facility Contacts

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Büşra Şirin Ahısha, MD

Role: primary

(0212) 856 27 40

Other Identifiers

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BeylikduzuStateH18

Identifier Type: -

Identifier Source: org_study_id

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