Effect of Virtual Reality on Patient's Comfort During Cardiac Electronic Device Implantation. (NCT06346132) | Clinical Trial Compass
RecruitingNot Applicable
Effect of Virtual Reality on Patient's Comfort During Cardiac Electronic Device Implantation.
Switzerland150 participantsStarted 2024-03-29
Plain-language summary
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.
Who can participate
Age range18 Years
SexALL
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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.
What they're measuring
1
Global pain intensity experienced during the procedure.