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Enrolling by invitation Observational

Muscle Function and Tenderness Differences in Headache Patients

NCT06859463 · tracked via the Priya Life Science Denmark tracker
Phase
Observational
Started
2025-02-28
Last updated
2025-03-10

Condition(s) studied

MigraineTension HeadachePosttraumatic Headache

Investigational drug(s) / intervention(s)

Muscle function

Muscle function: Functional evaluation First, the patients will fill the Fysisk Aktivitet Questionnaire, the o Klinisk Oral Fysiologi (KU) Questionnaire and the Harvard Trauma Questionnaire. Then, the evaluator will applicate the Total Tenderness Score (TTS) for evaluating their tenderness in different spots of the head and neck regions. The next evaluation comprehends the evaluation of the maximal voluntary isometric contraction (MVIC) for the different neck movements and the rate of force development (RFD) of the shoulder elevation. After this, patients will perform the cranio-cervical flexion test (CCFT), and, finally, the Ito test to evaluate the lumbar endurance.

Study summary

This cross-sectional study aims to compare muscle function of the neck, and shoulder and muscle tenderness in three groups of headache patients: migraine, tension-type headache, and posttraumatic headache. The study will evaluate muscle tenderness through the Total Tenderness Score (TTS) and muscle function through maximum voluntary isometric contraction (MVIC) and rate of force development (RFD). Additionally, functional assessments such as the Cranio-Cervical Flexion Test (CCFT) and Ito Test will be performed.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria:Criteria: Inclusion Criteria: * Aged 18 to 65 years. * Diagnosis of migraine, tension-type headache, or posttraumatic headache, occurring at least 10 days per month. * For tension-type headache patients, maximum of 3 days per month with migraine. Exclusion Criteria: * Pregnancy. * Significant psychiatric comorbidities (e.g., severe depression). * Medication-overuse headache. * Severe osteoarthritis in the neck or shoulder, or cervical disc herniation. Exclusion Criteria: \-

Primary outcome measure(s)

  • Primary Outcome Measure: 1.Rate of Force Development (RFD) — 1 year
    Rate of Force Development (RFD) of the shoulder elevation Maximum voluntary isometric contraction performed "as fast and hard as possible" using a custom dynamometer for the shoulder elevation movement.

Trial sites (1)

FacilityCityRegionStatus
Danish Headache Center Copenhagen Region H
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 NCT06859463 on ClinicalTrials.gov ↗ ← All trials in Denmark