VR Interventions to Reduce the Prevalence of Delirium in ICU Patients
Effects of Multi-model Virtual Reality Intervention Method to Reduce the Prevalence of Delirium in ICU Patients With Mechanical Ventilation
Peking Union Medical College Hospital
102 participants
Dec 18, 2023
INTERVENTIONAL
Conditions
Summary
The goal of this clinical trial is to learn the effect of Virtual Reality Family Support System (VRFS) on reducing delirium in ICU mechanically ventilated patients. The main question it aims to answer is: ·Using VRFS for participant intervention, can it reduce the incidence of delirium and improve clinical outcomes? Researchers will investigate whether the implementation of VRFS can reduce the number of delirium days and improve clinical outcomes. Participants will: * Receive the VRFS intervention until the endotracheal tube (ETT) is removed. * Have physiological data collected, including EEG, oxygen saturation levels, ECG, and blood pressure. * Keep a diary of delirium, dosage of sedative and analgesic drugs, the duration of mechanical ventilation, and ICU stays.
Eligibility
Inclusion Criteria3
- Mechanical ventilation duration is expected to be greater than 24 hours;
- ICU stay duration is expected to be greater than 72 hours;
- Age is 18 years or older, with no upper age limit;
Exclusion Criteria5
- Severe visual or auditory impairments (diplopia, low vision due to macular degeneration, retinopathy; severe hearing loss or deafness);
- Cognitive and consciousness disturbances prior to ICU admission;
- Severe motion sickness;
- Head trauma or surgery that prevents the wearing of equipment;
- A history of long-term use of antipsychotic and/or benzodiazepine medications.
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Interventions
Participants wear VR headsets and experience immersive virtual environments, where their family members will be present and offer companionship and comfort.
Locations(1)
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NCT05525702