Actively Recruiting
VR Interventions to Reduce the Prevalence of Delirium in ICU Patients
Led by Peking Union Medical College Hospital · Updated on 2026-03-27
102
Participants Needed
1
Research Sites
158 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
VR Interventions to Reduce the Prevalence of Delirium in ICU Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
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.
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
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Trial Site Locations
Total: 1 location
1
PUMC
Beijing, Beijing Municipality, China, 100730
Actively Recruiting
Research Team
Y
Yingying Yang, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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