Effect of Virtual Reality on Patient's Comfort During Cardiac Electronic Device Implantation.
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorSchlotterbeck Hervé
About this trial
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 criteria
Qualifiers
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.
Disqualifiers
Communication limitations,
Surgical procedure planned in sedation or narcosis,
Severe sensorial deficits (visual, auditory),
Claustrophobia,
Trial design
Treatments tested in this trial
- Virtual reality application
Treatment groups
150 Participants
are divided into 2 treatment groupsSponsors and collaborators
Schlotterbeck Hervé
Lead sponsor
Ente Ospedaliero Cantonale, Bellinzona
Sponsor institution
Source ClinicalTrials.gov