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Идёт набор NCT06138925

Analysis of the Psychometric Properties of Kinematic Parameters of Locomotion Measured by Inertial Measurement Units. Validation in Healthy Children and Children With Cerebral Palsy

Без фазы С лечением Cerebral Palsy

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: Analysis of walking, Analysis of running, Analysis of walking.
Кому может быть актуально
Состояния в реестре: Cerebral Palsy. Базовые параметры: 7 лет — 17 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
Франция
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

Обзор

Cerebral palsy (CP) is currently one of the major causes of disability in children. The presence of various disorders (muscle stiffness, architectural bone defects, spasticity) leads to a number of functional impacts, including severe impairment of mobility, particularly locomotion. Locomotion can be assessed using a motion capture system that enables 3-dimensional analysis, in order to help make treatment decisions and quantify them. Although these systems are currently considered to be the gold standard, the fact remains that they cause a certain amount of patient fatigue (long set-up times) and that walking is assessed in a laboratory rather than in real life. Today, technological advances have brought to the fore other gait analysis devices, such as inertial measurement units (IMUs). Various systems incorporating IMUs in the feet, for example, respond to these problems of analysing walking in real-life situations. The IMUs record the movements and orientation of the foot in space; the data is then processed by algorithms to recognise walking steps and calculate the spatio-temporal parameters of locomotion. Additional IMUs positioned on the body can be grafted onto this system to provide a more precise analysis of locomotion, in particular by calculating the movements of the various joints of the lower limb. However, before such devices can be used in a pathological paediatric population, they must be validated in a healthy population. This validation must be conducted using a precise method that has been widely documented in the COSMIN recommendations (Consensus-based Standards for the selection of health Measurement Instruments). The first stage will assess the safety of the IMU devices in a healthy paediatric population, and the validity of the spatio-temporal parameters. If these properties are deemed to be compliant, these same parameters will be assessed in a paediatric population with cerebral palsy in the second stage.

Вмешательства

  • Другое Analysis of walking
    3-dimensional gait analysis with inertial measurement units (IMUs) on flat ground at different speeds (slow, comfortable and fast)
  • Другое Analysis of running
    analysis of running on flat ground at different speeds (comfortable and fast)
  • Другое Analysis of walking
    3-dimensional gait analysis with inertial measurement units (IMUs) on flat ground at spontaneous speed (comfortable).

Первичные конечные точки

  • Walking speed [Срок оценки: During the study visit]

Критерии участия

Критерии включения

  • Children who have given their consent and whose legal representatives have given their consent
  • Age between 7 and 17 years,
  • Children able to understand simple commands and instructions.
  • Children living within a maximum radius of 50 km of the investigation site.
  • Child covered by national health insurance.

PATIENT GROUP (IN ADDITION TO THOSE ABOVE)

  • Children with proven cerebral palsy resulting in locomotor impairment but able to move around without technical aids (cane, wheelchair).
  • Child covered by national health insurance.

Критерии исключения

  • Children with a condition other than cerebral palsy that affects their ability to walk.
  • Child subject to a measure of legal protection
  • A child unable to give consent
  • Pregnant, parturient or breast-feeding participant

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

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Не применимо
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Другое

Центры проведения

Франция · 1 центр
  • Chu Dijon Bourgogne — Dijon

Идентификаторы

NCT: NCT06138925 · ORNETTI 2023

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗