Overview
The purpose of this study is to assess the effect on patient's comfort of a virtual reality experience during a procedure of cardiac electronic device implantation under local anesthesia.
Eligibility
Inclusion Criteria:
- Patients over 18 year old,
- Patients who signed the consent form and accepted to participate to the trial,
- New cardiac electronic device implantation or cardiac electronic device battery change,
- Surgical procedure planned in ambulatory care.
Exclusion Criteria:
- Communication limitations,
- Surgical procedure planned in sedation or narcosis,
- Severe sensorial deficits (visual, auditory),
- Claustrophobia,
- Known motion sickness,
- Patient isolated or with contact precautions,
- Known or anticipated psychiatric diseases,
- Patient known for epilepsia,
- Opened scar and or ongoing infection at the level of the face and/or eyes,
- Patient evaluated non suitable for the study by the surgeon, cardiologist or anesthetist.