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Идёт набор NCT07230002

Effects of Moderate/Severe Traumatic Brain Injury in the Subacute or Chronic Phase on Locomotor Strategies Involved in Navigation in Complex Virtual Environments

Без фазы С лечением Traumatic Brain Injury

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: Locomotion in a virtual reality setting.
Кому может быть актуально
Состояния в реестре: Traumatic Brain Injury. 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
Франция
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

Обзор

While clinical assessment of locomotor function in this population is carried out using tasks involving walking in a straight line without any obstacles, it does not take into account ecological situations (i.e., situations comparable to real-life situations) in which the person interacts with their environment, such as walking down a street with other pedestrians, which is fundamental to everyday life. This research therefore aims to study the social navigation skills during locomotion of people who have suffered a moderate or severe head injury in the chronic phase in more ecological tasks. This will provide a better understanding of the difficulties encountered by these patients during locomotor interactions in everyday life.

Вмешательства

  • Другое Locomotion in a virtual reality setting
    Patients and participants will be asked to perform several walking/locomotion tasks in a virtual evironment setting. The setting in question is a concert in a parc. The participants will have to walk towards the stage whilst avoiding bumping into "virtual people". A total of 5 different tasks (walking in a straight line, walking between people etc) will be completed for each participant. Different variables will then be recorded and extracted such as walking speed, interpersonnal distances, eye

Первичные конечные точки

  • Perceptive dimension : Elements of the environment viewed : Distribution (in %) [Срок оценки: From enrollment to the end of the participation at maximum 30 days]
  • Perceptive dimension : Elements of the environment viewed : Distance (in meters) [Срок оценки: From enrollment to the end of the participation at maximum 30 days]
  • Perceptive dimension : Elements of the environment viewed : duration of fixations (in milliseconds) [Срок оценки: From enrollment to the end of the participation at maximum 30 days]
  • Cognitive dimension : characteristics of the path taken : length of the path taken (in meters) [Срок оценки: From enrollment to the end of the participation at maximum 30 days]
  • Cognitive dimension : characteristics of the path taken : interpersonal distances with virtual humans (in m) [Срок оценки: From enrollment to the end of the participation at maximum 30 days]
  • Action-related dimension : walking speed (measured in m/s) [Срок оценки: From enrollment to the end of the participation at maximum 30 days]
Вторичные конечные точки (5)
  • " Montréal Cognitive Assesment " (MoCA) [Срок оценки: On day 1]
  • " 10-Meter Walking Test " (10MWT) [Срок оценки: At day 1]
  • Balance test : ABC-scale [Срок оценки: At day 1]
  • Balance test : "Berg Balance Scale" (BBS) [Срок оценки: At day 1]
  • Balance test : "Time Up and Go" (TUG) [Срок оценки: At day 1]

Критерии участия

Inclusion Criteria for Traumatic Brain Injury group :

  • 18 ≤ Age ≤ 55 years old
  • Male/female
  • Having suffered a first non-penetrating head injury
  • Moderate to severe severity with initial Glasgow Coma Scale score 5<GCS<13
  • In the subacute or chronic phase (≥ 3 months at the date of the experiment, relative to the date of the injury)
  • Able to walk (10WMT speed ≥ 0.8 m/s, able to walk at least 20 m without technical or human assistance, PM ≥ 300 m)
  • Able to maintain dynamic balance while standing (TUG<16s)
  • Able to answer simple questionnaires, according to the investigator's judgment
  • Having given their free, informed, expressed (written) consent
  • Registered with a social security system
  • Individuals under legal protection measures such as guardianship may be eligible

Inclusion Criteria for healthy control group :

  • 18 ≤ Age ≤ 55 years old
  • Male/female
  • Able to walk (≥ 0.8 m/s, able to walk at least 20 m without technical or human assistance, PM ≥ 300 m)
  • Able to answer simple questionnaires, according to the investigator's judgment
  • Having given free, informed, expressed (written) consent
  • Registered with a social security system

Exclusion Criteria specific to patients in the traumatic brain injury group :

\- Person under legal protection (excluding guardianship) or unable to express consent

Exclusion Criteria for both groups :

  • Severe patho-psychiatric care underway, which may impact the conduct of the protocol, at the investigator's discretion
  • Presence of neurological signs suggestive of a neurodegenerative disease responsible for gait disturbance (Parkinson's syndrome, Alzheimer's disease, etc.)
  • Individuals with musculoskeletal disorders that impact their locomotor abilities
  • Presence of uncontrolled epilepsy at the time of inclusion
  • Presence of visual impairments that make experimentation impossible, at the discretion of the investigator
  • Pregnant, parturient, or breastfeeding women
  • Participants in another ongoing research protocol involving human subjects

Exclusion Criteria for healthy control group :

  • Presence of fatigue, trauma, or a condition affecting mobility, posture, balance, or walking
  • Persons deprived of their liberty by a judicial or administrative decision
  • Persons deprived of their liberty by judicial or administrative decision
  • Persons under legal protection (guardianship, curatorship, judicial protection) or unable to express their consent
  • Persons undergoing severe psychiatric treatment or admitted to a health or social care facility for purposes other than research.

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

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Не применимо
Модель
Одна группа
Маскирование
Открытое
Основная цель
Фундаментальное исследование

Центры проведения

Франция · 1 центр
  • Fondation Saint Helier — Rennes

Идентификаторы

NCT: NCT07230002 · 2025-A00679-40

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗