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
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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Interventions
DEVICEVirtual reality application
In this group, virtual reality will be added to usual care
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06346132
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