Меню
Идёт набор NCT07250672

Patient-Specific 3D Action Observation Training in Parkinson's Disease

Без фазы С лечением Parkinson Disease Virtual Reality Action Obervation Training Immersive Virtual Reality

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: Patient-Specific VR Action Observation Training, Healthy-Model VR Action Observation Training.
Кому может быть актуально
Состояния в реестре: Parkinson Disease, Virtual Reality, Action Obervation Training, Immersive Virtual Reality. Базовые параметры: 50 лет — 85 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

Examining the Effect of Action Observation Training Using Patient-Specific 3D Records in Parkinson's Patients

Обзор

Although studies exist demonstrating the effects of single-session action observation training on bradykinesia in patients with Parkinson's disease, research investigating the long-term application of such training remains limited. Furthermore, the broader literature indicates that action observation training has typically been conducted in simulated environments or by using recordings obtained from healthy individuals. The aim of the present study is to examine the effects of action observation training, delivered in a fully immersive virtual reality environment using each patient's own 3D motion recordings, on bradykinesia and other disease-related parameters.

Подробное описание

Action observation training has been applied across diverse populations to improve performance and treat pathological conditions. Considering that bradykinesia tends to manifest more prominently in rhythmic movements, studies in healthy individuals have shown that merely observing rhythmic actions can influence spontaneous finger movement speed and lead to changes in motor performance, thereby paving the way for the use of action observation in addressing bradykinesia. In a study investigating the effects of action observation in patients with Parkinson's disease, observing fast rhythmic finger movements was reported to increase spontaneous finger movement speed, and compared with acoustic training, the effect of action observation persisted longer over time. Research on imagery through action observation further indicates that immersive virtual reality headsets, compared to monitor screens, facilitate the development of more distinct spatial rhythmic patterns in the brain. This evidence supports the use of fully immersive VR headsets instead of non-immersive monitor-based systems in action observation training.

Вмешательства

  • Другое Patient-Specific VR Action Observation Training
    Participants will receive immersive VR action observation training using their own 3D motion recordings captured with an Insta360 camera (Arashi Vision Inc., Shenzhen, China). In Parkinson's patients, only the initial movement sequences without bradykinetic slowing will be selected, and these will be extended to the desired duration using loop playback or ping-pong loop playback in the device's proprietary software. The action observation protocol will consist of the following one-minute tasks:
  • Другое Healthy-Model VR Action Observation Training
    Participants will receive immersive VR action observation training using 3D video recordings of the same activities performed by healthy individuals, captured with an Insta360 camera (Arashi Vision Inc., Shenzhen, China). Recordings will not require editing or adjustments. The action observation protocol will consist of the same one-minute tasks: (1) total finger abduction and adduction, (2) fist making and opening, (3) wrist flexion and extension, (4) forearm pronation and supination, and (5) r

Первичные конечные точки

  • Spontaneous Movement Rate (SMR [Срок оценки: At baseline and after completion of 6-week intervention period]
Вторичные конечные точки (5)
  • Unified Parkinson's Disease Rating Scale (UPDRS) [Срок оценки: At baseline and after completion of 6-week intervention period]
  • Nine-Hole Peg Test (NHPT) [Срок оценки: At baseline and after completion of 6-week intervention period]
  • Disabilities of the Arm, Shoulder and Hand Questionnaire (DASH) [Срок оценки: At baseline and after completion of 6-week intervention period]
  • Parkinson's Disease Questionnaire (PDQ-8) [Срок оценки: At baseline and after completion of 6-week intervention period]
  • Intrinsic Motivation Inventory (IMI) [Срок оценки: After completion of 6-week intervention period]

Критерии участия

Критерии включения

  • Voluntary agreement to participate in the study
  • Clinical diagnosis of Parkinson's disease confirmed by a neurologist
  • Ongoing treatment with antiparkinsonian medication
  • Hoehn and Yahr (H-Y) stage ≤ 3
  • Ability to walk independently

Критерии исключения

  • Presence of additional neurological disorders other than Parkinson's disease
  • Change in medication dosage within the past month
  • Score of ≥ 10 on the Simulator Sickness Questionnaire
  • Presence of amblyopia, strabismus, or pathologies impairing focus, depth perception, or normal 3D vision
  • Failure on the butterfly test of the Titmus stereotest (greater than 3,552 seconds of arc)

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
  • Abant Izzet Baysal University Faculty of Health Science — Bolu

Идентификаторы

NCT: NCT07250672 · AIBU-FTR-BENLI-009

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗