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Набор скоро начнётся NCT07261384

"Personalized Physiotherapy for Migraine: Effects on Pain, Fatigue, and Physical Function"

Без фазы С лечением Migraine

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Personalized Structured Physiotherapy Intervention, Standard Treatment.
Кому может быть актуально
Состояния в реестре: Migraine. Базовые параметры: 18 лет — 55 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Turkey (Türkiye)
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

"Investigation of the Effects of Individually Tailored Physiotherapy Approaches on Pain, Fatigue, and Physical Function in Individuals With Migraine: A Randomized Controlled Trial"

Обзор

Migraine is a prevalent neurological disorder associated with pain, fatigue, and reduced physical function. The aim of this randomized controlled trial is to examine the effects of a personalized and structured physiotherapy program-including cervical spine stabilization exercises, vestibular rehabilitation, and pain neuroscience education-on pain intensity, fatigue, and functional outcomes in individuals with migraine. Participants will be randomly allocated to an intervention group receiving personalized physiotherapy or a control group receiving standard physiotherapy care. Outcomes will be assessed at baseline, post-intervention, and follow-up.

Подробное описание

Migraine is a disabling primary headache disorder characterized by recurrent attacks and frequently accompanied by cervical musculoskeletal dysfunction, vestibular symptoms, and altered pain processing mechanisms. Current evidence suggests that physiotherapy interventions targeting manual therapy, cervical stabilization, vestibular function, and pain neuroscience education may positively influence migration-related outcomes; However, studies combining these components in a personalized treatment model are limited.

This randomized controlled trial aims to investigate the effectiveness of a personalized structured physiotherapy program designed specifically for individuals with migraine. The interventions will include manual therapy, cervical spine stabilization exercises, vestibular rehabilitation strategies, and pain neuroscience education delivered by a physiotherapist. The control group will receive only pain neuroscience education.

Primary outcomes will include pain intensity and frequency. Secondary outcomes will include fatigue, disability level, cervical function, physical performance, and patient-reported functional limitations. Assessments will be conducted at baseline, immediately post-intervention, and during a follow-up period. The findings are expected to contribute to evidence-based physiotherapy approaches for migraine management.

Вмешательства

  • Другое Personalized Structured Physiotherapy Intervention
    The manual therapy will include component, applied according to individual patient needs to reduce pain, improve mobility, and modulate neuromuscular control. The cervical spine stabilization exercises will target deep neck flexors and cervical postural muscles to improve neuromuscular control, endurance, and motor coordination. The vestibular rehabilitation component will include gaze stabilization, habituation, and balance exercises tailored to migraine-related vestibular symptoms. The PNE
  • Другое Standard Treatment
    Participants continue routine care including medications prescribed by their physician. Only two 40-minute Pain Neuroscience Education sessions over 8 weeks. No physiotherapy or exercise intervention provided.

Первичные конечные точки

  • Pain Intensity (VAS) [Срок оценки: Baseline, Week 8]
Вторичные конечные точки (11)
  • Pain Frequency (MIDAS A Question) [Срок оценки: Baseline and Week 8]
  • Fatigue (Modified Fatigue Impact Scale - MFIS) [Срок оценки: Baseline and Week 8]
  • Migraine Disability (MIDAS Total Score) [Срок оценки: Baseline and Week 8]
  • Quality of Life (Headache Impact Test - HIT-6) [Срок оценки: Baseline and Week 8]
  • Craniovertebral Angle (Forward Head Posture) [Срок оценки: Baseline and Week 8]
  • Cervical Range of Motion [Срок оценки: Baseline and Week 8]
  • Deep Cervical Flexor Muscle Performance [Срок оценки: Baseline and Week 8]
  • Trigger Point Tenderness / Pressure Pain Threshold [Срок оценки: Baseline and Week 8]
  • Neck Pain Intensity (VAS) [Срок оценки: Baseline, Week 8]
  • Dizziness Handicap (DHI) [Срок оценки: Baseline and Week 8]
  • Balance (Mini-BESTest) [Срок оценки: Baseline and Week 8]

Критерии участия

Критерии включения

  • Aged between 18 and 55 years
  • Diagnosed with migraine according to the International Classification of Headache Disorders - 3rd edition (ICHD-3) criteria
  • Experiencing 2-8 migraine attacks per month in the last 3 months
  • Able to participate in an 8-week physiotherapy intervention program
  • Able to understand instructions and provide written informed consent
  • Stable medication use for migraine for at least 1 month prior to participation (no changes planned during study period)

Критерии исключения

  • • Presence of other primary headache disorders (cluster headache, tension-type headache as primary diagnosis, etc.)
  • Neurological diseases (epilepsy, stroke, multiple sclerosis)
  • Vestibular disorders unrelated to migraine
  • Cervical radiculopathy, myelopathy, or severe cervical spine pathology
  • History of neck surgery or significant cervical trauma
  • Severe musculoskeletal conditions affecting posture or cervical function
  • Pregnancy or breastfeeding
  • Participation in another clinical trial within the last 3 months
  • Inability to attend intervention sessions or complete outcome assessments

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Простое слепое
Основная цель
Лечение

Центры проведения

Turkey (Türkiye) · 1 центр
  • Erzincan Binali Yıldırım Univercity, Medicine Faculty — Erzincan

Идентификаторы

NCT: NCT07261384 · E-10333602-050.04-291274

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗