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Clinical Trials in Turkey / NCT07656922
Recruiting Observational

Scapular Muscle Activation and Shoulder Performance in Migraine

NCT07656922 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-04-01
Last updated
2026-06-18

Condition(s) studied

MigraineUpper ExtremityMuscle Activity

Study summary

Migraine is a significant health problem due to its high prevalence and substantial contribution to disability. Individuals with migraine have been reported to exhibit myofascial trigger points, increased pain sensitivity, and altered muscle activation patterns, particularly in the trapezius muscles. As the upper and middle trapezius muscles play critical roles in scapular stability and movement, alterations in these muscles may affect scapular orientation and upper extremity function. However, studies investigating the relationship between trapezius muscle activation, scapular orientation, and upper extremity performance in individuals with migraine are limited. Therefore, this study aimed to compare trapezius muscle activation, scapular orientation, and upper extremity performance between individuals with and without migraine. We hypothesized that individuals with migraine would exhibit altered upper and middle trapezius muscle activation, impaired scapular orientation, and reduced upper extremity performance compared with healthy controls.

Eligibility

Sex
ALL
Min age
18 Years
Max age
55 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Aged 18-55 years * Diagnosed with migraine by a neurologist according to the ICHD-3 criteria * Experiencing at least 3 migraine attacks per month * Willing to participate and provide written informed consent Exclusion Criteria: * Presence of other types of headache disorders * History of trauma, fracture, or surgery involving the cranio-cervical region, scapular region, or upper extremity * Presence of neurological or inflammatory rheumatic diseases * Presence of psychiatric disorders * Receiving physiotherapy or rehabilitation for migraine or the cervical, thoracic, or upper extremity regions within the past 6 months * Cognitive impairment affecting the understanding of test instructions

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Ankara Yıldırım Beyazıt University Ankara Çubuk Recruiting

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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 NCT07656922 on ClinicalTrials.gov ↗ ← All trials in Turkey