Effect of a Virtual Reality Program on Patient Comfort in the Surgical Intensive Care Unit

NANot yet recruitingINTERVENTIONAL
Enrollment

194

Participants

Timeline

Start Date

September 30, 2025

Primary Completion Date

September 30, 2027

Study Completion Date

October 31, 2027

Conditions
Immersive Virtual RealityDiscomfortIPREAIntensive Care UnitDelirium
Interventions
DEVICE

HypnoVR

In the intervention group, after extubation, patients will receive IVR with HypnoVR®, twice-a-day over two to five days. The product consists of HypnoVR® virtual reality software and HypnoVR® Compagnon remote control software. HypnoVR® is a CE-marked class 1 medical device, developed and marketed by HypnoVR SAS, an ISO 13484:2016 and ISO 27001:2017 certified company. The device works with a virtual reality headset, a personal audio device and a mobile terminal. The investigators will only use sessions of 10 to 20 minutes. For each type of session, a visual universe, a musical atmosphere and a male or female voice are defined. Typically, the scenarios include 3 phases: preparation, hypnosis and return. We will use the following sessions: anxiety, pain, rehabilitation.

OTHER

usual health care

usual health care

Trial Locations (1)

80054

CHRU Amiens, Amiens

All Listed Sponsors
lead

Centre Hospitalier Universitaire, Amiens

OTHER

NCT06830369 - Effect of a Virtual Reality Program on Patient Comfort in the Surgical Intensive Care Unit | Biotech Hunter | Biotech Hunter