Virtual Reality in Reducing Acute Orthopedic Pain

Обзор

The primary aim of this research is to show that a virtual reality (VR) service line is feasible and can sustain itself with the ability to take care of patients. Additionally, the investigators aim to learn about the limitations of a service line and provide a pathway for future improvements in building a VR service line that is optimally aligned with the user's needs. Secondary aims are to evaluate the clinical aspects of the patient's outcomes including length of stay, morphine equivalents in pain medicine required during the hospital stay, and user experiences.

Вмешательства

• Другое virtual reality
  Virtual reality program to reduce pain in orthopedic fractures

Первичные конечные точки

• opioid use [Срок оценки: From date of enrollment which begins at hospital admission until the date of hospital discharge, assessed up to 5 weeks]

Вторичные конечные точки (4)

• reduction in anxiolytics [Срок оценки: From date of enrollment which begins at hospital admission until the date of hospital discharge, assessed up to 5 weeks]
• hospital length of stay [Срок оценки: From date of enrollment which begins at hospital admission until the date of hospital discharge, assessed up to 5 weeks]
• reduction in sleep aids prescribed [Срок оценки: From date of enrollment which begins at hospital admission until the date of hospital discharge, assessed up to 5 weeks]
• User experiences [Срок оценки: obtained once on the day of hospital discharge, up to 5 weeks from study enrollment]

Критерии участия

Критерии включения

• Hospitalized with an orthopedic fracture
• Able to participate fully in all aspects of the study
• Able to understand and sign informed consent
• Individuals with unaided vision or those who can correct their vision using contact lenses

Критерии исключения

• Non-English speaking
• Self-reported history of acute and/or chronic severe motion sickness
• The presence of a facial/head deformity that will prohibit the wearing of a VR head mounted display.
• Legally blind or deaf
• Have had a seizure within the past 1 year
• Have current (within the past 30 days) clinically significant acute or chronic progressive or unstable/uncontrolled neurologic disorder
• Have a known history of any condition or factor judged by the investigator to preclude participation in the study or which might hinder adherence

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

Открытое

Основная цель

Лечение

Центры проведения

США · 1 центр

• Mayo Clinic Hospital — Jacksonville

Идентификаторы

NCT: NCT06624969 · 24-009261

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

Открыть это исследование на ClinicalTrials.gov ↗