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Pediatric Preoperative Virtual Reality Program

The Influence of a Pre-Operative Preparatory Virtual Reality Program on the Self-Assessed Anxiety of Children Undergoing Elective Surgery

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03957525
Acronym
PPVRP
Enrollment
11
Registered
2019-05-21
Start date
2019-08-01
Completion date
2020-03-31
Last updated
2020-04-20

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

Conditions

Anxiety, Surgery

Keywords

Virtual reality, Pediatric, Anxiety, Surgery, Anesthesia, Intervention, Exposure, Randomized controlled trial, Pediatric urology, Orthopedic surgery, General Pediatric surgery, Pediatric orthopedics

Brief summary

Does the introduction of a preparatory virtual reality (VR) program that is used in the home environment, have an effect on the anxiety level of children immediately before surgery, prior to administration of preoperative sedatives?

Detailed description

Up to 60% of children who require elective surgery report significant anxiety in the preoperative setting. Severe perioperative anxiety of a child poses a major challenge for the surgeon, since it is often accompanied by adverse behavioral and emotional reactions and associated with a complicated operative and postoperative course. The investigators have made the personal experience that informing the children ahead of time about what to expect in the hospital, decreases child anxiety and increases parent satisfaction. There is considerable debate on the best way how to inform children about what to expect during their hospital stay. The investigators had a virtual reality application developed that introduces the children to several aspects of the hospital environment. Therefore, these children now ahead of time what they will experience during their hospital stay. The aim is to evaluate the effect of this preparatory virtual reality application on the anxiety level of children immediately before surgery.

Interventions

OTHERPre-Operative Preparatory Virtual Reality Program

The Influence of a Pre-Operative Preparatory Virtual Reality Program on the Self-Assessed Anxiety of Children Undergoing Elective Surgery

Sponsors

Thoralf Liebs
Lead SponsorOTHER

Study design

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

Intervention model description

Prospective randomized, controlled trial

Eligibility

Sex/Gender
ALL
Age
7 Years to 13 Years
Healthy volunteers
No

Inclusion criteria

1. The child is between the age of 7 and 13 years 2. The child is undergoing an elective surgical procedure under general anesthesia 3. The child understands Swiss German 4. The parent(s) understand(s) German 5. The parent(s) possess a smart phone 6. Internet access is given 7. The patient information has been explained 8. Informed Consent is signed

Exclusion criteria

1. The child has a hearing impairment 2. The child has neurologic disorder 3. The child requires postoperative intensive care 4. The child has previous experience of anesthesia 5. American Society of Anesthesiologists (ASA) score of III or greater

Design outcomes

Primary

MeasureTime frameDescription
Perioperative anxiety level of children immediately before surgery (VAS-A)2 - 90 days after recruitingPerioperative anxiety level of children as measured by the Visual Analog Scale for Anxiety (VAS-A), immediately before surgery, prior to administration of preoperative sedatives (T2). The VAS-A scale consists of a 10 cm long, horizontal line, supplemented by two labels: no anxiety or fear at the left end, worst possible anxiety or fear at the right end of the scale.

Secondary

MeasureTime frameDescription
Perioperative anxiety level of Children VAS-A2 - 90 days after recruitingPerioperative anxiety level of children measured at T0, T1 and T3 with VAS-A.
Perioperative anxiety level of Children VFAS2 - 90 days after recruitingPerioperative anxiety level of children as measured by the Visual Faces Analog Scale (VFAS) scale at T0, T1, T2 and T3. The VFAS scale consists of six different drawings of faces, supplemented by labels as follows: (Anxiety Level:, none, mild, mild-moderate, moderate, moderate-high, highest)
Perioperative anxiety level of accompanying parent14 - 110 days after recruitingPerioperative anxiety level of accompanying parent measured at T0, T1 and T2 with the VAS-A and VFAS scale
Non-disease specific secondary Outcomes14 - 110 days after recruitingThe investigators want to evaluate to which extent the VR program is able to improve the patient and parent's level of preparedness for surgery. Unfortunately, there are currently no validated outcome measures available covering these issues. Therefore, we developed a questionnaire assessing the level of preparedness related to seven aspects of the hospital stay, which are particularly illustrated by the VR program.

Countries

Switzerland

Outcome results

None listed

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