Pilot Study on the Evaluation of the Effectiveness of a Virtual Reality Device on Anxiety During Procedural Sedation in Traumatology in Emergency Department

Exclusion Criteria

• •Patients suffering from mono or binocular blindness
• •Patient under the influence of alcohol or psychotropic drugs
• •Patient presenting a psychosis and/or a state of agitation, and/or a state of confusion.
• •Patient presenting a hemodynamic, respiratory or neurological failure
• •Patient with at least one of the following symptoms at the time of inclusion in the study: headache, dizziness, nausea, vomiting
• •Persons benefiting from reinforced protection, i.e. minors, persons deprived of their liberty by a judicial or administrative decision, adults under legal protection (guardianship and trusteeship) and finally patients in a vital emergency situation.
• •Pregnant or breastfeeding women, women of childbearing age who do not have effective contraception (hormonal/mechanical: per os, injectable, transcutaneous, implantable, intrauterine device, or surgical: tubal ligation, hysterectomy, total oophorectomy)
• •Concurrent participation in another clinical research study whose objective is the evaluation of anxiety and/or pain