Impact of Foot Mobility Techniques on Balance and Pressure in Young Adults
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: Specific foot mobility.
- Кому может быть актуально
- Состояния в реестре: Healthy. Базовые параметры: от 18 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
- Португалия
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
Effects of Specific Foot Mobility Techniques on Biomechanical and Functional Parameters in Young Adults: A Randomized Controlled Trial
Обзор
This study aims to evaluate the effectiveness of specific foot mobility techniques on functional and biomechanical parameters of the foot in young adults aged 18 to 24 years. The study employs a randomized controlled trial design with the following key components: Key outcomes include: Baropodometric pressures (measured using a baropodometric platform). Balance (evaluated through the Y-Balance Test). Navicular height (assessed using the Navicular Drop Test) Anterior functional reach (measured through functional reach test)
Подробное описание
This study explores the immediate and short-term effects of specific foot mobility techniques on functional and biomechanical outcomes in healthy young adults. The research is grounded in the growing recognition of the foot's critical role in postural control, balance, and lower-limb biomechanics.
The intervention consists of foot mobility techniques designed to improve joint mobility and overall foot function. These techniques will be applied bilaterally. The study employs a randomized controlled trial design, with participants randomly allocated to either the experimental group (receiving the intervention) or the control group (receiving no treatment during the intervention period).
Participants are assessed at three time points:
Baseline (M0): Before the intervention. Immediately Post-Intervention (M1). Follow-Up (M2): 24 hours after the intervention.
The primary outcomes include:
Changes in plantar pressure distribution and postural control as measured by a baropodometric platform.
Balance performance assessed through the Y-Balance Test. Navicular height variation evaluated using the Navicular Drop Test. Anterior functional reach, measured by Functional Reach Test. The study focuses on identifying measurable improvements in functional and biomechanical parameters that may enhance clinical approaches to foot health and rehabilitation. By targeting a young and healthy population, the research aims to establish a foundation for further studies in other age groups and clinical conditions. This work aims to contribute to evidence-based practices in manual therapy and foot biomechanics.
Вмешательства
- Другое Specific foot mobility
Specific mobility of the foot, performed bilaterally.
Первичные конечные точки
- Balance - Y balance test [Срок оценки: M0: Before intervention; M1: Immediately after intervention; M2: 24h after intervention.]
- Baropodometric pressure [Срок оценки: M0: Before intervention; M1: Immediately after intervention; M2: 24h after intervention.]
- Navicular height - Navicular drop test [Срок оценки: M0: Before intervention; M1: Immediately after intervention; M2: 24h after intervention.]
- Anterior functional reach - functional reach test [Срок оценки: M0: Before intervention; M1: Immediately after intervention; M2: 24h after intervention.]
Критерии участия
Критерии включения
- minimum age of 18 years.
Критерии исключения
- pregnant women,
- individuals with lesions in the lower limbs in the last 12 months,
- history of congenital deformity in the lower limb
- presence of vestibular or balance disorders
- users of corrective insoles or orthoses.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Да
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Параллельные группы
- Маскирование
- Двойное слепое
- Основная цель
- Другое
Центры проведения
Португалия · 1 центр
- Escola Superior de Saúde do Vale do Ave — Vila Nova de Famalicão
Идентификаторы
NCT: NCT06817798 · Foot mobility_2025