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Perioperative Effects of Operating Room Virtual Tour

The Effects of Operating Room Virtual Tour on Preoperative Anxiety, Emergence Delirium and Postoperative Behavioral Changes of Pediatric Patients: Prospective, Randomized, and Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03172182
Enrollment
86
Registered
2017-06-01
Start date
2017-08-01
Completion date
2017-10-11
Last updated
2020-03-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Emergence Delirium, Postoperative Complications, Preoperative Care

Brief summary

Preoperative anxiety is associated with adverse consequences such as emergence delirium, and postoperative behavioral changes. According to previous studies, providing information of anesthetic procedures helps to lessen preoperative anxiety. However, verbal explanation alone provides the limited effect, and the tour program of the operating room prior to surgery may not be possible for a number of hospitals due to organizational and financial reasons. Therefore, the virtual reality (VR) tour of the operating room may be an innovative and novel method to give children information about the preoperative process and to alleviate the preoperative anxiety. In this study, we intend to evaluate the effects of the operating room virtual tour on preoperative anxiety as well as emergence delirium and postoperative behavioral changes, in pediatric patients.

Interventions

BEHAVIORALa 360-degree VR video tour

At operation day, pediatric patients of the VR group and their parents are educated using virtual tour program explaining preoperative procedures and showing environment of the operating room. A 360-degree virtual reality (VR) video for the tour program was filmed in advance and is provided using a head mount device into which a smartphone is installed, at 30 minutes before the induction of anesthesia.

Sponsors

Seoul National University Bundang Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
4 Years to 10 Years
Healthy volunteers
No

Inclusion criteria

* Elective surgery * American Society of Anesthesiologist (ASA) physical class I, II * Informed consent; Children aged between 4 and 6 years old are allowed to have verbal consent and their parents provide informed written consent. Children over the age of 7 are required to obtain a written consent with parental permission.

Exclusion criteria

* ASA class ≥ III * Major surgery needing postoperative intensive care unit (ICU) admission. * Chronic disease or history of preterm birth * Developmental delay * Hearing or vision impairment * Affective disorder * History of epilepsy or seizure * Previous experience of general anesthesia

Design outcomes

Primary

MeasureTime frameDescription
Emergence deliriumAt 5 minutes after arrival in post-anesthesia care unit (PACU)Pediatric Anesthesia Emergence Delirium (PAED) scale

Secondary

MeasureTime frameDescription
Preoperative anxiety2 times; before the intervention (baseline) and, at waiting area, before the operating room entrance (preoperative)Modified Yale Preoperative Anxiety Scale (mYPAS)
Postoperative behavioral change2 times; on the 1st and 14th day (2 weeks) after the surgery, we will call and talk with the parentsHospitalization Post- Hospitalization Behavior Questionnaire for Ambulatory Surgery (PHBQ-AS)

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026