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Clinical Trials in Turkey / NCT06948903
Recruiting Observational

Relationship Between Central Sensitization Symptoms and Cognitive Dysfunction in Fibromyalgia

NCT06948903 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2023-01-10
Last updated
2025-09-12

Condition(s) studied

FibromyalgiaCognitive DysfunctionCentral Sensitisation

Investigational drug(s) / intervention(s)

Central Sensitization InventoryThe Montreal Cognitive AssessmentCognitive Symptom Severity Scale-ExtendedFibromyalgia Impact QuestionnaireNumeric rating scaleHospital Anxiety and Depression Scale

Central Sensitization Inventory: The Central Sensitization Inventory is used by some researchers to investigate pain sensitivity through symptoms associated with central sensitization and related comorbidities. It can help determine the severity of central sensitization. The scale was developed to detect central sensitization in patients with chronic pain and consists of two sections: Section A and Section B. For scoring purposes, only Section A is used. A score of 40 or higher out of 100 is associated with an increased likelihood of central sensitization.

The Montreal Cognitive Assessment: The Montreal Cognitive Assessment was initially developed as a test for mild cognitive impairment, but has also been determined to match qualities of the mini mental state examination 80. It assesses seven areas of cognition for a total possible score of 30 points. A score of 21 or less is indicative of cognitive impairment in Turkish population.

Cognitive Symptom Severity Scale-Extended: The Cognitive Symptom Severity Scale extends the scale of the original cognitive symptom severity scale. Participants are asked to rate their cognitive symptoms related to concentration and memory on a single scale ranging from 1-5, rather than the original 1-3, where higher scores indicate greater severity.

Fibromyalgia Impact Questionnaire: The Fibromyalgia Impact Questionnaire is composed of 10 items. The first item contains 11 questions related to physical functioning - each question is rated on a 4 point Likert type scale. Items 2 and 3 ask the patient to mark the number of days they felt well and the number of days they were unable to work (including housework) because of fibromyalgia symptoms. Items 4 through 10 are horizontal linear scales marked in 10 increments on which the patient rates work difficulty, pain, fatigue, morning tiredness, stiffness, anxiety and depression. The maximum scale score is 100, with higher scores associated with increasing disability.

Numeric rating scale: Numeric Rating Scale will be used to determine pain intensity during assessments. Participants will be asked to rate their pain intensity by selecting a value between 0 and 10. Higher scores are associated with increased pain severity.

Hospital Anxiety and Depression Scale: This scale is used to assess anxiety and depression symptoms and consists of 14 items (7 items for anxiety, 7 items for depression). For each subscale, scores range from 0 to 21: • 0-7 points: No symptoms or very mild symptoms • 8-10 points: Moderate symptoms • 11 points or higher

Study summary

The aim of the study is to investigate the relationship between central sensitization parameters and cognitive dysfunction in patients with fibromyalgia.The main questions it aims to answer are:

Do central sensitization symptoms affect cognitive dysfunction in patients with fibromyalgia? To what extent do central sensitization symptoms affect objective and subjective cognitive complaints in fibromyalgia patients? How do cognitive complaints relate to other clinical parameters, including disease severity, in these patients?

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Being diagnosed with fibromyalgia according to American College of Rheumatology 2016 criteria * Being between 18-65 years old * Being literate * Accepting to participate in the study Exclusion Criteria: * Concomitant systemic inflammatory disease, central nervous system disease (cortical involvement), active infection and malignancy history * History of illness that may lead to cognitive impairment * Being \<18 and \>65 years old * Being illiterate * Not accepting to participate in the study

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Health Sciences University Istanbul Uskudar Recruiting

More Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06948903 on ClinicalTrials.gov ↗ ← All trials in Turkey