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VR Interventions to Reduce the Prevalence of Delirium in ICU Patients

RecruitingNAAges 18 Years - 90 YearsAllPeking Union Medical College Hospital
NCT05525702 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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.

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📋 Eligibility rules (as published)
Inclusion Criteria * 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; * Language: Chinese. Exclusion Criteria * 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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What it tests

  • VRFS
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Where

1 site
PUMC
Beijing, China
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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