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Набор скоро начнётся NCT07565688

Forward Head Posture Correction on Cerebral Oxygenation During Dual-task in Symptomatic Subjects

Без фазы С лечением Forward Head Posture Neck Pain

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: Forward Head Posture Correction.
Кому может быть актуально
Состояния в реестре: Forward Head Posture, Neck Pain. Базовые параметры: 18 лет — 35 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
ОАЭ
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Effects of Forward Head Posture Correction on Prefrontal Cerebral Oxygenation During Cognitive-Motor Interference in Symptomatic Subjects With Forward Head Posture: A Randomized Controlled Trial

Обзор

This study aims to investigate the effects of forward head posture correction on neck pain, brain activity, and cognitive-motor performance. Forward head posture is a common postural problem, especially among young adults who spend long hours using smartphones and computers. It is frequently associated with neck pain, reduced mobility, and functional limitations. Emerging evidence also suggests that this postural deviation may influence brain function and increase the mental effort required during tasks that involve both thinking and movement. Participants with forward head posture and neck pain will be recruited and randomly assigned to one of three groups: an intervention group using a cervical traction device (Denneroll), a sham group using a towel roll, or a control group receiving no intervention. The intervention will be performed at home over a six-week period, with sessions conducted five times per week. The duration of each session will gradually increase based on participant tolerance to ensure safety and comfort. All participants will undergo assessments at baseline and after the intervention period. Pain intensity will be measured using a standardized pain scale. Brain activity will be assessed using a non-invasive technique called functional near-infrared spectroscopy (fNIRS), which measures changes in oxygen levels in the brain. Participants will also perform balance tasks under single-task and dual-task conditions, where they will be asked to maintain balance while performing simple cognitive tasks. In addition, cognitive function will be evaluated using standardized tests of attention, memory, and overall cognitive performance. This study will help determine whether correcting forward head posture can reduce pain and improve brain and cognitive function. The findings may provide valuable insights into the relationship between posture, pain, and brain activity, and may contribute to the development of more effective and comprehensive rehabilitation approaches for individuals with forward head posture.

Подробное описание

Forward head posture (FHP) is a common postural deviation associated with neck pain, impaired sensorimotor control, and functional limitations. In addition to musculoskeletal effects, emerging evidence suggests that FHP may influence cortical activity, particularly within prefrontal regions involved in attention and cognitive-motor integration. Individuals with FHP have demonstrated increased cognitive-motor interference during dual-task performance, indicating greater reliance on cortical resources and reduced motor automaticity. However, it remains unclear whether correcting FHP can reduce pain and modify these neurophysiological responses.

This study aims to investigate the effects of forward head posture correction on pain intensity as a primary outcome, alongside task-evoked cerebral oxygenation and cognitive-motor interference. A prospective, single-blinded, randomized controlled trial design with three parallel groups will be used. Participants with symptomatic FHP will be randomly allocated to an intervention group receiving Denneroll cervical traction, a sham group receiving a non-therapeutic towel roll intervention, or a control group receiving no intervention.

The intervention will be conducted over six weeks, with participants in the intervention and sham groups performing home-based sessions with gradual progression in duration to ensure safety and tolerance. All participants will undergo assessments at baseline and post-intervention.

Pain intensity will be evaluated using the Visual Analog Scale (VAS). Neurophysiological outcomes will be assessed using functional near-infrared spectroscopy (fNIRS) to measure changes in oxygenated and deoxygenated hemoglobin in the prefrontal cortex during rest, single-task, and dual-task conditions. Cognitive-motor interference will be examined using dual-task paradigms that combine balance tasks with cognitive demands. Cognitive function and balance performance will also be evaluated using standardized assessments.

The procedures used in this study are non-invasive and associated with minimal risk. The fNIRS device does not emit radiation, and the intervention may cause only mild and temporary discomfort, which will be minimized through gradual progression and monitoring. Participants will be informed of their right to withdraw at any time without consequences.

By integrating clinical, cognitive, and neurophysiological outcomes, this study aims to provide a comprehensive understanding of the effects of forward head posture correction. The findings may contribute to the development of more effective, mechanism-based rehabilitation strategies targeting both pain and brain function in individuals with forward head posture.

Вмешательства

  • Другое Forward Head Posture Correction
    Duration: 6 weeks Frequency: 5 sessions per week (total 30 sessions) Setting: Home-based Position: Supine Session duration: Starts at \~3 minutes, progressively increased to 15-20 minutes (as tolerated) \- Intervention: DG: The denneroll will be given under the cervical spine (based on deviation level) TG: A towel roll will be given as an intervention CG: No intervention This protocol simultaneously examines cerebral oxygenation using functional near-infrared spectroscopy (fNIRS)(HbO and HbR)

Первичные конечные точки

  • The visual analog scale [Срок оценки: Outcome measures will be collected at baseline (week 0) and after completion of the intervention (week 6).]
Вторичные конечные точки (5)
  • functional near-infrared spectroscopy [Срок оценки: Outcome measures will be collected at baseline (week 0) and after completion of the intervention (week 6).]
  • Symbol Digit Modalities Test [Срок оценки: Outcome measures will be collected at baseline (week 0) and after completion of the intervention (week 6).]
  • Brief Visuospatial Memory Test-Revised [Срок оценки: Outcome measures will be collected at baseline (week 0) and after completion of the intervention (week 6).]
  • Montreal Cognitive Assessment [Срок оценки: Outcome measures will be collected at baseline (week 0) and after completion of the intervention (week 6).]
  • Technobody Balance System (Balance performance) [Срок оценки: Outcome measures will be collected at baseline (week 0) and after completion of the intervention (week 6).]

Критерии участия

Критерии включения

  • Young adults of both sexes aged 18-35 years
  • Individuals with forward head posture (a craniovertebral angle (CVA) < 50°)
  • Presence of neck pain with an intensity of ≥3 on the Visual Analog Scale (VAS)
  • Ability to understand and follow basic English instructions
  • No cognitive impairment (score >18 on the Montreal Cognitive Assessment (MoCA))

Критерии исключения

  • History of cervical spine surgery or significant cervical trauma
  • Currently receiving physiotherapy or rehabilitation for cervical spine conditions
  • Individuals on medications (diagnosed neurological disorders)

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

ОАЭ · 1 центр
  • University of Sharjah — Sharjah city

Идентификаторы

NCT: NCT07565688 · REC-26-04-23-05-PG

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗