Overview
The main objective of this study is to evaluate, in vigilant resuscitation patients, the effect of the use of HYPNO VR on the pain felt during the insertion of a thoracic drain.
Description
This is a prospective, randomized, open-label, monocentric, prospective study of two parallel groups of patients in whom a chest tube is to be inserted:
- Group 1: Insertion of the drain according to the usual management protocol.
- Group 2: Insertion of the drain according to the usual management protocol supplemented by the use of a hypnosis software application (HYPNO-VR).
Eligibility
Inclusion Criteria:
- Patient 18 years of age or older, having read and signed the consent form for participation in the study
- Patient admitted to intensive care whose state of health requires the insertion of a thoracic drain according to the doctor in charge of the patient.
Exclusion Criteria:
- Patient under legal protection, guardianship or trusteeship
- Pregnant or breastfeeding patient
- Patient not affiliated to the French social security system
- Hearing or visual disturbances contraindicating the use of virtual reality headphones
- Inability to provide the subject with informed information and/or written informed consent: dementia, psychosis, consciousness disorders, non-French speaking patient
- Unbalanced epilepsy
- Contraindication to local anaesthesia, one of the analgesics or sleeping pills used in the protocol
- Need for drainage in a life-threatening emergency (respiratory distress or compressive pleural effusion)
- Concurrent participation in other research or during a period of exclusion from previous research