Effectiveness of Virtual Reality-enhanced Interventions on Preoperative Anxiety in Adults Undergoing Elective Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorSin Lun CHAN

About this trial

Brief Summary: Preoperative anxiety is a common phenomenon in surgical patients, with a pooled global prevalence of 48%. Surgical patients with preoperative anxiety may negatively impact their psychological health and surgical outcomes. Recent studies have revealed the promising effects of virtual reality-enhanced interventions to improve preoperative anxiety symptoms among adults undergoing elective surgery.

There is a lack of interventional studies to compare and evaluate the co-designed preoperative virtual reality-enhanced interventions in adult surgical patients.

This study aims to examine the effects of co-designed virtual reality educational video and virtual reality distraction video on preoperative anxiety symptoms, vital signs, Satisfaction with Life Scale (SWLS), and postoperative anxiety compared to usual care. This study will contribute by evaluating evidence-based, user-centered VIPA that may be effective for improving preoperative anxiety among adult surgical patients.

Eligibility criteria

Qualifiers

Age aged ≥18 years old

Surgical patients attending Nurse Pre-anaesthetic Assessment Clinic (NPAC)

American Society of Anesthesiology (ASA) physical status ASA I or ASA II

Able to communicate in Chinese

Disqualifiers

Patients who have a cognitive, communication or physical impairment precluding their ability to complete the study

Patients who are prone to epilepsy or other neurological conditions

Trial design

Treatments tested in this trial

  • Virtual Reality

Treatment groups

270 Participants
are divided into 3 treatment groups

Sponsors and collaborators

Sin Lun CHAN

Lead sponsor

Chinese University of Hong Kong

Sponsor institution