Immersive Care - Virtual Reality(VR) 360 Pediatric Surgery Preparation.

NCT04658030 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2021-04-01

No results posted yet for this study

Summary

Context: This study is part of the larger Immersive Care project which (in short) seeks the connection between technology and care by conducting feasibility studies with promising technological interventions tailored to care.

This is one of the case studies from the larger project titled: 360 ° video VR surgery preparation: feasibility, acceptability, tolerability and initial effectiveness of virtual reality for children in a Flemish hospital.

Domain: This scientific study will take place in 1 hospital on the pediatric ward. The target group consists of children between 6 and 12 years of age who will undergo an operation, the parents and the care providers involved.

Target:

1. Assess the acceptability, feasibility and tolerability of the 360 ° video VR surgery preparation.
2. Assess the effectiveness of the 360 ° video VR surgery preparation on preoperative procedural anxiety in children, comparing the intervention with care as usual (CAU \*).

* CAU in this study is a picture book which is a kind of animated video with text to explain what will happen on the day of the operation.

Conditions

  • Surgery

Interventions

DEVICE

VR 360 video surgery preparation

Preparing children on the surgery by a virtual reality 360 degrees video tour from the pediatric ward to the surgery room. In this video all information is given necessary for the surgery. This takes a maximum of 30 minutes and will be performed 1 time.

OTHER

Care as usual

Preparing the children for surgery with the care as usual. A booklet that can be viewed by the children and parents at home.

Sponsors & Collaborators

  • Heilig Hart Ziekenhuis Lier

    collaborator UNKNOWN
  • Fotosfeer

    collaborator UNKNOWN
  • Thomas More University of Applied Sciences

    lead OTHER

Principal Investigators

  • Wessel van de Veerdonk, PhD · Thomas More University of Applied Sciences

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
6 Years
Max Age
12 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-03-01
Primary Completion
2021-09-30
Completion
2021-09-30

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04658030 on ClinicalTrials.gov