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Идёт набор NCT06797492

Virtual Reality for Shoulder Rehabilitation

Без фазы С лечением Shoulder Musculoskeletal Disorders

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: Shoulder Physical Examination, Shoulder Rehabilitation in a Virtual Environment, Usability assessment and presence and co-presence evaluation.
Кому может быть актуально
Состояния в реестре: Shoulder Musculoskeletal Disorders. Базовые параметры: 18 лет — 75 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
Италия
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Virtual Reality for Shoulder Rehabilitation: New Approaches and Applications in Orthopedics

Обзор

Goal: The clinical investigation involves the evaluation of the usability level of the VR system, sense of presence, and co-presence during the execution of various rehabilitation exercises through specific questionnaires. Participant Population: The study will enroll 50 patients with shoulder musculoskeletal disorders will be enrolled Main Questions: * How does the integration of Virtual Reality (VR) in rehabilitation programs impact the usability of the system for patients with shoulder musculoskeletal disorders? * To what extent does the sense of presence experienced by patients using VR systems influence their motivation and adherence to rehabilitation exercises? * How do patients with shoulder musculoskeletal disorders perceive the co-presence in VR rehabilitation scenarios, and how does it affect their overall treatment experience? Participant Tasks: * Shoulder Physical Examination * Instructions to the patient on exercises to be performed using Oculus and selection of customizable settings on the VR app * Execution of the protocol developed for shoulder rehabilitation in a virtual environment * Evaluation of the usability of the VR system, sense of presence, and co-presence through different validated scales

Подробное описание

Musculoskeletal disorders are recognized globally as a primary cause of pain and physical disability. Among these, shoulder pathologies impose significant limitations, affecting patients' range of motion, quality of life, and daily functionality, often leading to substantial physical and occupational restrictions. Effective rehabilitation is essential for restoring functionality in patients with such disorders.

Traditionally, rehabilitative therapy relies on manual interventions by physiotherapists, which, while beneficial, can be hindered by logistical challenges, including limited accessibility to treatment facilities and professional availability. Additionally, at-home unsupervised exercises often suffer from low adherence due to reduced motivation and lack of engagement.

Technological advances in recent years have led to the development of novel rehabilitation strategies, particularly in virtual reality (VR) systems, which hold promising applications in musculoskeletal rehabilitation. VR provides a patient-centered, customizable approach that can adapt exercises to the individual's needs, making rehabilitation more engaging and accessible, especially for patients facing physical barriers to in-person care. Additionally, VR technology enables precise tracking of patient movements, offering an objective alternative to traditional assessments reliant on subjective observation and clinical scales.

Despite these advancements, the integration of VR into rehabilitative protocols for MSDs remains underexplored. This clinical study aims to assess the usability, sense of presence, and co-presence of VR systems in patients with shoulder musculoskeletal disorders across four rehabilitation phases. Evaluating these factors through validated questionnaires will provide critical insights into optimizing patient engagement and satisfaction, which are key to enhancing therapeutic outcomes and aligning rehabilitation interventions with patient-specific needs.

Вмешательства

  • Диагностический тест Shoulder Physical Examination
    shoulder physical examination is conducted to assess the patient's musculoskeletal condition and to track progress throughout the rehabilitation phases
  • Процедура Shoulder Rehabilitation in a Virtual Environment
    The rehabilitation protocol for shoulder disorders is executed using a Virtual Reality (VR) system, where patients perform customized exercises tailored to their physical characteristics.
  • Другое Usability assessment and presence and co-presence evaluation
    The usability of the VR system, along with the sense of presence and co-presence during rehabilitation, is assessed using validated scales

Первичные конечные точки

  • Change in Usability Level of the VR System Using the System Usability Scale (SUS) [Срок оценки: Across four rehabilitation phases: T1 (0-4/6 weeks), T2 (6-12 weeks), T3 (12-20 weeks), and T4 (beyond 20 weeks)]
Вторичные конечные точки (2)
  • Change in Sense of Presence Using the Igroup Presence Questionnaire (IPQ) [Срок оценки: The sense of presence will be evaluated across four rehabilitation phases: T1 (0-4/6 weeks), T2 (6-12 weeks), T3 (12-20 weeks), and T4 (beyond 20 weeks)]
  • Change in Co-Presence Using the Networked Minds Social Presence Inventory [Срок оценки: The co-presence will be assessed across four rehabilitation phases: T1 (0-4/6 weeks), T2 (6-12 weeks), T3 (12-20 weeks), and T4 (beyond 20 weeks).]

Критерии участия

Критерии включения

  • Patients with shoulder musculoskeletal disorders
  • Patients aged 18-75 years
  • Patients who have signed informed consent

Критерии исключения

  • Patients with insufficient cognitive and language functions to follow instructions provided by clinicians and/or experimenters involved in the project
  • Patients who do exhibit impediments that could hinder the use of VR devices

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
Другое

Центры проведения

Италия · 2 центра
  • Fondazione Policlinico Universitario Campus Bio-Medico — Roma
  • Fondazione Policlinico Universitario Campus Bio-Medico — Rome

Идентификаторы

NCT: NCT06797492 · 234.24 CET2 cbm · PNC0000007 - CUP: B53C22006980

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗