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

This trial does not accept healthy volunteers

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

Design model

Parallel

Treatments tested in this trial

  • Virtual Reality

    Other intervention

    The Virtual Reality-enhanced Interventions on Preoperative Anxiety for adults undergoing elective surgery (VIPA) was developed based on theoretical basis, systematic review evidence, and qualitative study.

Treatment groups

270 Participants
are divided into 3 treatment groups
Group A: Virtual Reality Group 1 (Education approach)Experimental treatment 1 intervention
Group B: Virtual Reality Group 2 (Distraction approach)Experimental treatment 1 intervention
Group C: Control GroupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Preoperative anxiety

Preoperative anxiety will be measured using the Short Chinese Version of the State-Trait Anxiety Inventory (Du et al., 2022). Items are rated on a 4-point Likert scale ranging from 1 to 4, with higher scores indicating higher anxiety. The Short Chinese Version of the State-Trait Anxiety Inventory demonstrates good psychometric properties.

Time frame
Baseline, Immediate post-intervention, Day of surgery

Secondary outcomes

1

Heart rate

Heart rate will be measured in beats per minute (bpm) using physiological monitors to provide a more objective measurement for anxiety.

Time frame
Baseline, Immediate post-intervention, Day of surgery
2

Blood pressure

Blood pressure will be measured in millimeters of mercury (mmHg) using physiological monitors to provide a more objective measurement for anxiety.

Time frame
Baseline, Immediate post-intervention, Day of surgery
3

Temperature

Temperature will be measured in degrees Celsius (°C) using tympanic thermometers to provide a more objective measurement for anxiety.

Time frame
Baseline, Immediate post-intervention, Day of surgery
4

Life satisfaction

Life satisfaction will be measured using the Chinese version of Satisfaction with Life Scale (SWLS) (Diener et al., 1985). Items are rated on a 7-point Likert scale ranging from 1 to 7, with higher scores indicating higher life satisfaction. The Chinese version of Satisfaction with Life Scale (SWLS) demonstrates good psychometric properties (Wu \& Yao, 2006).

Time frame
Baseline, Immediate post-intervention, Day of surgery, Post-operative day 7

Other outcomes

Sponsors and contacts

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Sin Lun CHAN

Lead sponsor

Chinese University of Hong Kong

Sponsor institution