Virtual Reality Interventions for Preoperative Anxiety
Effectiveness of Virtual Reality-enhanced Interventions on Preoperative Anxiety in Adults Undergoing Elective Surgery
Recruiting
N/AInterventional Study
Preoperative Anxiety
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
270 (estimated)
Sponsor
Sin Lun CHAN · Other
Who this trial is looking for
This trial is looking for adults undergoing elective surgery who experience preoperative anxiety. Participants will take part in virtual reality sessions designed to help reduce their anxiety before surgery.
Are You a Good Fit for This Trial?
You may be able to join if
I am at least 18 years old
I am attending a Nurse Pre-anaesthetic Assessment Clinic
I have an American Society of Anesthesiology (ASA) physical status of ASA I or ASA II
I can communicate in Chinese
You may not be able to join if
I have a cognitive impairment that affects my ability to complete the study
I have a communication impairment that affects my ability to complete the study
I have a physical impairment that affects my ability to complete the study
I am prone to epilepsy or other neurological conditions
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
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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 elect…
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.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 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
Exclusion Criteria:
* Patients who have a cognitive, communication …
Inclusion Criteria:
* 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
Exclusion Criteria:
* 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
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