Clinical Trials Directory

Trials / Suspended

SuspendedNCT05617638

Impact of Virtual Reality (e-Nature VR) During Hospitalization in Adult Intensive Care Unit

Status
Suspended
Phase
N/A
Study type
Interventional
Enrollment
212 (estimated)
Sponsor
Hospital Israelita Albert Einstein · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Randomized clinical trial to analyze the perceived impact of the virtual reality intervention on the experience of pain and well-being, and the influence on vital signs and the relationship with the length of stay in the intensive care unit.

Detailed description

The highly specialized and complex technology used in intensive care units to provide continuous monitoring of the patient health context makes possible to increase the survival of patients with critical and unstable clinical status, but increases the triggering factors of the stress of hospitalized patients. Staying in these therapy units is accompanied by additional stress, confusional mental states, cognitive dysfunction, and depression. Virtual reality is a technique that involves the use of computer technology to create the effect of an interactive three-dimensional world in which objects have a spatial presence reducing the suffering related to a medical procedure, without side effects and without the need for additional personnel. Actual exposure to nature can be difficult to achieve for patients admitted to intensive care. Therefore, exposure to nature via media devices, and virtual reality (VR) is considered a promising technology due to its advantage in creating a sense of immersion. Furthermore, some evidence indicates that virtual nature can improve attentional resources, cognitive performance, and pain experience. This clinical trial aims to analyze the influence of VR use in patients of Intensive Care Unit (ICU). After informed the consent form, participants will be randomly into control and intervention groups. Blood pressure, heart rate, respiratory rate, oxygen saturation will be evaluated, in addition to the experience of well-being and pain immediately before and immediately after the intervention for 2 consecutive days.The hypothesis of the study is that VR will positively influence vital signs and lived experiences, which will consequently reduce the length of stay in the ICU.

Conditions

Interventions

TypeNameDescription
BEHAVIORALInterventionParticipants will watch nature images in virtual reality from the e-Natureza VR Database for 20 minutes for 2 consecutive days.

Timeline

Start date
2023-06-27
Primary completion
2024-05-01
Completion
2025-06-25
First posted
2022-11-15
Last updated
2025-06-26

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT05617638. Inclusion in this directory is not an endorsement.