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

Inclusion Criteria: * Patient aged 18 years or older * Patient suffering from one of the following traumatic pathologies requiring a technical procedure in the emergency room Shoulder dislocation Ankle dislocation Elbow dislocation Wrist dislocation Reducible fractures * No contraindication to Virtual Reality * No contraindication to morphine, ketamine, propofol, paracetamol, nefopam and MEOPA * Patient having given oral, free and informed consent 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