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  3. Virtual reality stimulation to reduce the incidence of delirium in critically ill patients: study protocol for a randomized clinical trial.
 

Virtual reality stimulation to reduce the incidence of delirium in critically ill patients: study protocol for a randomized clinical trial.

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BORIS DOI
10.48350/153738
Date of Publication
March 1, 2021
Publication Type
Article
Division/Institute

ARTORG Center - Geron...

Universitätsklinik fü...

Universitätsklinik fü...

Author
Naef, Aileen
ARTORG Center - Gerontechnology and Rehabilitation
Jeitziner, Marie-Madlen
Universitätsklinik für Intensivmedizin
Gerber, Stephan Moreno
ARTORG Center - Gerontechnology and Rehabilitation
Jenni-Moser, Béatrice Monika
Universitätsklinik für Intensivmedizin
Müri, René Martinorcid-logo
Universitätsklinik für Neurologie
Jakob, Stephan
Universitätsklinik für Intensivmedizin
Nef, Tobiasorcid-logo
ARTORG Center - Gerontechnology and Rehabilitation
Universitätsklinik für Neurologie
Hänggi, Matthiasorcid-logo
Universitätsklinik für Intensivmedizin
Subject(s)

600 - Technology::610...

Series
Trials
ISSN or ISBN (if monograph)
1745-6215
Publisher
BioMed Central
Language
English
Publisher DOI
10.1186/s13063-021-05090-2
PubMed ID
33648572
Uncontrolled Keywords

Critical care Deliriu...

Description
BACKGROUND

Delirium has been long considered as a major contributor to cognitive impairments and increased mortality following a critical illness. Pharmacologic and non-pharmacologic strategies are used against delirium in the intensive care unit (ICU), despite these strategies remaining controversial. Previous studies have shown the feasibility of using virtual reality within the ICU setting, and we propose to use this technology to investigate the effect of immersive virtual reality stimulation on the incidence of delirium in the ICU. Moreover, we propose to use motion sensors to determine if patient movement patterns can lead to early prediction of delirium onset.

METHODS

This study is conducted as a randomized clinical trial. A total of 920 critically ill patients in the ICU will participate. The control group will receive standard ICU care, whereas the intervention group will, in addition to the standard ICU care, receive relaxing 360-degree immersive virtual reality content played inside a head-mounted display with noise-cancelling headphones, three times a day. The first 100 patients, regardless of their group, will additionally have their movement patterns recorded using wearable and ambient sensors. Follow-up measurements will take place 6 months after discharge from the ICU.

DISCUSSION

Delirium is widely present within the ICU setting but lacks validated prevention and treatment strategies. By providing patients with virtual reality stimulation presented inside a head-mounted display and noise-cancelling headphones, participants may be isolated from disturbances on an ICU. It is believed that by doing so, the incidence of delirium will be decrease among these patients. Moreover, identifying movement patterns associated with delirium would allow for early detection and intervention, which may further improve long-term negative outcomes associated with delirium during critical care.

TRIAL REGISTRATION

ClinicalTrials.gov NCT04498585 . Registered on August 3, 2020.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/56436
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2021_-_Naef_-_Trials_-_PMID_33648572.pdftextAdobe PDF781.25 KBpublishedOpen
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