Evaluation of Pain and Anxiety in Patients With an Invasive Procedure in Emergencies (URGENCES_RV)
Virtual Reality

About this trial
This is an interventional treatment trial for Virtual Reality focused on measuring pain, anxiety
Eligibility Criteria
Inclusion Criteria:
- Man and woman (age ≥ 18 years)
- Francophone
- Patient with medical insurance
- Patient with a wound requiring trunk or limb sutures
- Or male patient requiring an urinary catheter
- Patient with cutaneous and subcutaneous wounds (deep plane possible) but without repair of noble tissues (tendons or fasciae) with no limit on the number of points to be made (i.e. without impact on the main endpoint).
Exclusion Criteria:
- Patient with a wound or skin infection of the face
- Patients with nausea, vomiting, dizziness
- Patients with a history of neurological disorders with epilepsy
- Patient whose investigator judges that he can not wear a virtual reality helmet
- Patient under tutorship or curatorship
- Patient deprived of liberty
- Refusal to participate in the study.
Sites / Locations
- Groupe Hospitalier Paris Saint-Joseph
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
Local anesthesia
local anesthesia + virtual reality
The study population will consist of consecutive pre-screened patients when they arrive at the emergency department at the level of the host nurse. The emergency physician who will be in charge of the patient gives the patient the information form and ensures the absence of contraindication, responds to the patient's questions and collects his free, informed and express consent. Once the patient is included, the group (with or without virtual reality) of the patient's participation in the study will be notified by the reception nurse and emergency referral: - Arm 1 (usual care): the procedure of care will be the same as usual.
The study population will consist of consecutive pre-screened patients when they arrive at the emergency department at the level of the host nurse. The emergency physician who will be in charge of the patient gives the patient the information form and ensures the absence of contraindication, responds to the patient's questions and collects his free, informed and express consent. Once the patient is included, the group (with or without virtual reality) of the patient's participation in the study will be notified by the reception nurse and emergency referral: - Arm 2 (intervention): local anesthesia + virtual reality