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Completed

NCT Number: NCT02449395

Cross-sectional Study of Fibromyalgia

This study is designed to collect data on precipitating factors, diagnosis, morbidity, therapy, quality of life, and symptom severity, etc. informations in patients with fibromyalgia.

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Key information

Conditions

Fibromyalgia Muscular Diseases Musculoskeletal Diseases Nervous System Diseases Neuromuscular Diseases Rheumatic Diseases

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Guang'anmen Hospital of China Academy of Chinese Medical Sciences

Beijing, Beijing Municipality, 100053, China

About this study

Patients fulfilling 1990 ACR criterion for fibromyalgia will be recruited in Fibromyalgia outpatient service which is belonged to the Department of Rheumatism. Except collecting patients' demographic and social characteristic informations, rheumatologist also carry out a comprehensive evaluation including patient current history, current medication use, and tender point examination for a diagnosis or confirmation of fibromyalgia and treatment recommendations. Patients with fibromyalgia will be asked to fill a set of questionnaires to evaluate their quality of life, symptoms severity, quality of sleep and emotion. The study will be conducted in Beijing, China.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 years or older.
  • Fulfills the American College of Rheumatology (ACR) 1990 classification criteria for Fibromyalgia.

Exclusion criteria

  • Don't fulfill any classification criterions for Fibromyalgia.

Treatment and study plan

Primary outcomes

  1. Fibromyalgia symptoms severity as measured by Fibromyalgia Impact Questionnaire (FIQ)

    Time frame: up to 1 week

Secondary outcomes

  1. QOL as measured by Short Form-36 Health Status Questionnaire (SF-36)

    Time frame: up to 1 week

  2. Pain scores as measured by Numerical rating scale (NRS)

    Time frame: up to 1 week

  3. Fatigue scores as measured by Multidimensional Assessment Fatigue (MAF)

    Time frame: up to 1 week

  4. Depression scores as measured by Beck depression inventory (BDI)

    Time frame: up to 1 week

  5. Stress scores as measured by Perceived Stress Scale (PSS)

    Time frame: up to 1 week

  6. Sleep scores as measured by Pittsburgh sleep quality index (PSQI)

    Time frame: up to 1 week

Sponsors and collaborators

Lead sponsor

Guang'anmen Hospital of China Academy of Chinese Medical Sciences

Other

Registry information

Official study title

A Cross-sectional Study of Fibromyalgia in Beijing

Important dates

Study start
2015
Primary completion
2016
Study completion
2018
First posted
May 20, 2015
Registry last updated
Nov 20, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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