RecruitingNot ApplicableNCT06346132

Effect of Virtual Reality on Patient's Comfort During Cardiac Electronic Device Implantation.

Effect of Virtual Reality on Patient's Comfort During Cardiac Electronic Device Implantation: a Randomized, Controlled Trial.

Sponsor

Schlotterbeck Hervé

Enrollment

150 participants

Start Date

Mar 29, 2024

Study Type

INTERVENTIONAL

Conditions

Virtual Reality

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.

Eligibility

Min Age: 18 Years

Inclusion Criteria4

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 Criteria10

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.

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