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

Sponsor
Thomas More University of Applied Sciences (Other)
Overall Status
Recruiting
CT.gov ID
NCT04658030
Collaborator
Heilig Hart Ziekenhuis Lier (Other), Fotosfeer (Other)
80
1
2
7
11.4

Study Details

Study Description

Brief 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.
Condition or Disease Intervention/Treatment Phase
  • Device: VR 360 video surgery preparation
  • Other: Care as usual
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
80 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
360° Video VR Surgery Preparation: Feasibility, Acceptability, Tolerability and Initial Effectiveness of Virtual Reality for Children in a Flemish Hospital.
Actual Study Start Date :
Mar 1, 2021
Anticipated Primary Completion Date :
Sep 30, 2021
Anticipated Study Completion Date :
Sep 30, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: VR 360 video surgery preparation

Preparing pediatric patients for surgery with a newly developed VR 360 degree video. Maximum 30 minutes, one time.

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.

Active Comparator: 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.

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.

Outcome Measures

Primary Outcome Measures

  1. Change from baseline in staff attitude towards the intervention [Staff: Measurement takes place in week 5 after the start of the study.]

    Unified theory of acceptance and use of technology tests the acceptance of the staff towards the intervention in this study. Assess change in patient attitude towards the intervention with the Unified Theory of Acceptance and Use of Technology (UTAUT) questionnaire survey. The UTAUT questionnaire survey for end-users consists of 20 items with five response options ranging from "Totally disagree" to "Totally agree". The questionnaire survey consists of 7 subscales, for most of which higher scores indicate a more positive attitude towards the intervention.

  2. Change from baseline in tolerability (Do participants experience symptoms of simulator sickness?) [Immediately after the intervention]

    Assessment of physical side effects after exposure to VR by the Pediatric Simulator Sickness Questionnaire (Peds SSQ). The Peds SSQ contains queries that probe 4 symptom categories: (1) eye strain (queries 1-4); (2) head and neck discomfort (queries 5 and 6); (3) sleepiness (solipsism) or fatigue (queries 7 and 8); and dizziness or nausea (visually induced motion sickness, queries 9-13). The scale that is used is a likert scale (with additional faces) ranging from 0 to 6 per query (0 = no of the above "complaints"; 6 = a lot of the above "complaints".

  3. Usability of the intervention: System Usability Scale (SUS) [Immediately after the intervention.]

    Assessment of ease of use of the intervention with the System Usability Scale (SUS). The SUS is a 10 item questionnaire with five response options for respondents; from "strongly disagree" to "strongly agree". A higher SUS score indicates better usability.

  4. Patient satisfaction: Client Satisfaction Questionnaire (CSQ-8) [Immediately after the intervention]

    Assessment of client satisfaction with the VR application with the Client Satisfaction Questionnaire (CSQ-8). The CSQ-8 consists of 8 items with four response options. Higher scores indicate higher satisfaction.

  5. Intervention adherence [Immediately after the intervention]

    Measure intervention adherence by registering the number of fully completed sessions.

  6. Procedure time [Immediately after the intervention]

    The procedure time of intervention in minutes

Secondary Outcome Measures

  1. Preliminary effectiveness (change in anxiety between timepoints) (Intervention and control) [Measurement 1: Immediately after signing the informed consent, day 1 of study. Measurement 2: Immediately after the intervention, day 1 of study. Measurement 3: Just before surgery, day 4 of study]

    Measuring procedural anxiety (with a Visual Analogue Scale) (1.Before intervention/control, 2. just after intervention/control and 3.just before surgery)

Eligibility Criteria

Criteria

Ages Eligible for Study:
6 Years to 12 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Written informed consent must be obtained

  • Inpatient or outpatient in the study site (Heilig Hart Hospital Lier): each paediatric patient who will undergo surgery during the study period (01-12-2020 and 30-09- 2021).

  • Age range of ≥ 6 and ≤ 12

  • Normal or corrected-to-normal vision

  • Normal or corrected-to-normal hearing

Exclusion Criteria:
  • Patient has a history of seizure disorders (e.g. epilepsy)

  • Physical impairment that preclude VR intervention (e.g. facial burns or wounds, contagious infectious disease, need for intensive care)

  • Non-Dutch/English/French speaker: Both the paediatric patient and his/her caregiver must be able to provide informed consent and assent

  • Previous enrolment in this study (during a previous hospital stay)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Heilig Hart Ziekenhuis Lier Lier Vlaanderen Belgium 2500

Sponsors and Collaborators

  • Thomas More University of Applied Sciences
  • Heilig Hart Ziekenhuis Lier
  • Fotosfeer

Investigators

  • Principal Investigator: Wessel van de Veerdonk, PhD, Thomas More University of Applied Sciences

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Thomas More University of Applied Sciences
ClinicalTrials.gov Identifier:
NCT04658030
Other Study ID Numbers:
  • IC_PED_2
First Posted:
Dec 8, 2020
Last Update Posted:
Apr 1, 2021
Last Verified:
Mar 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Thomas More University of Applied Sciences

Study Results

No Results Posted as of Apr 1, 2021