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Recruiting NCT06533410

Using the Chinese Indigenization FS Scale in the Diagnosis of Fibromyalgia： Specificity and Sensitivity in Clinical Practice

— Observational Fibromyalgia

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: The FM Diagnosis and Assessment Scale will be filled out, and there will be no other interventions beyond that.
Who it may be relevant to
Registry conditions: Fibromyalgia. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

This study aimed to evaluate the specificity and sensitivity of the diagnostic criteria for fibromyalgia after conducting local validation in China.

Interventions

  • Diagnostic test The FM Diagnosis and Assessment Scale will be filled out, and there will be no other interventions beyond that
    The FM Diagnosis and Assessment Scale will be filled out, and there will be no other interventions beyond that

Primary outcome measures

  • Diagnosis of fibromyalgia with the Polysymptomatic Distress Scale(PDS) [Time frame: up to 1 week]
Secondary outcome measures (6)
  • QOL as measured by Short Form-36 Health Status Questionnaire(SF-36) [Time frame: up to 1 week]
  • Fibromyalgia symptoms severity as measured by the Rebised Fibromyalgia Impact Questionnaire(FIQR) [Time frame: up to 1 week]
  • Depression scores as measured by Beck depression inventory(BDI) [Time frame: up to 1 week]
  • Stress scores as measured by Perceived Stress Scale(PSS) [Time frame: up to 1 week]
  • Sleep scores as measured by Pittsburgh sleep quality index(PSQI) [Time frame: up to 1 week]
  • Fatigue was measured by the Multidimensional Fatigue Inventory(MFI-20) [Time frame: up to 1 week]

Eligibility criteria

Inclusion criteria

  • At least 18 years of age; Patients with chronic widespread pain; Able to complete the questionnaire.

Exclusion criteria

  • Terminal patients with severe psychiatric diseases, tumors, systemic lupus erythematosus, systemic sclerosis, or other serious diseases.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

China · 1 center
  • Guang'anmen Hospital — Beijing

Identifiers

NCT: NCT06533410 · 2024-121-KY

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗