Virtual Reality to Reduce the Anxiety in Critically Ill Patient

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity Hospital, Toulouse

About this trial

Anxiety and discomfort generated by repeated medical cares and invasive procedures can induce cognitive disorders in critical illness survivors as post-traumatic stress disorder. For this reason, managing patients' anxiety is particularly important in the intensive care unit. Physicians have recently started using immersive virtual reality (VR), based on real-time interaction with an artificial 360° immersive world, as an adjunctive non-invasive and non-pharmacological anxiolysis technique. The purpose of this project is to assess the virtual reality stimulation to reduce anxiety in Intensive Care Unit (ICU) patients.

Eligibility criteria

Qualifiers

Adult patient

Oral consent after free and informed information

Hospitalized in the multipurpose intensive care unit of Rangueil hospital with an estimated length of stay greater than 24 hours

Conscious (Glasgow Coma Scale > 8) and Richmond Agitation-Sedation Scale (RASS) sedation score between -1 and +1

Disqualifiers

Patient under legal protection (guardianship or curatorship)

RASS < -1 or > +1

Visual or hearing difficulties preventing the use of the VR headset

Severe psychiatric history (severe depression, psychosis, bipolarity), advanced dementia or mental retardation

Trial design

Treatments tested in this trial

  • Virtual Reality

Treatment groups

128 Participants
are divided into 2 treatment groups

Sponsors and collaborators