The Effect of Virtual Reality on Postoperative Pain and Anxiety in Cardiac Surgery.

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAcademisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

About this trial

The objective of this study is to investigate the effect of VR on post-operative pain and anxiety management in cardiac surgery patients undergoing a coronary artery bypass grafting (CABG) procedure.

Participants in the intervention group will receive a 20 minute session with the head mounted VR device on post-operative days 1,2 and 3.

Participants in the control group will be treated with conventional post-operative care.

Eligibility criteria

Qualifiers

Age ≥18 years or older with written informed consent

Patients undergoing surgical CABG

Disqualifiers

Major comorbidities besides coronary artery disease

Complicated surgical procedure

Hearing and/or visual impairments

Psychiatric impairments

Trial design

Treatments tested in this trial

  • Virtual Reality distraction therapy

Treatment groups

100 Participants
are divided into 2 treatment groups