VR Interventions to Reduce the Prevalence of Delirium in ICU Patients
Recruiting
N/A
Interventional Study
Delirium
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 90
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 102 (estimated)
- Sponsor
- Peking Union Medical College Hospital · Other
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About This Trial
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 n…
Trial Locations
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Eligibility Criteria
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, …
Contacts