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The goal of this randomized controlled trial is to evaluate whether a virtual reality based preparation method can efficiently decrease the proportion of children requiring general anesthesia during MRI examinations.
Participants will take part in a virtual reality environment resembling an MRI before their scheduled MRI examination.
Researchers will compare these children to usual care and a booklet based preparation method to see if less children need anesthesia for completing the MRI examination.
Study Description:
Our study investigates the efficacy of a custom-made virtual reality experience in the preparation of children for MRI examinations. We hypothesise that preparation with VR can significantly reduce the need for anesthesia in children during MRI examinations, or if anesthesia is needed less doses of anesthetics are required.
Objectives:
Primary Objective:
To evaluate whether the VR based preparation decreases the need for anesthesia and sedation during MRI examinations.
Secondary Objectives:
To evaluate whether fear, mood, anxiety, familiarity with the MRI examination of the children and willingness to take part again change as a result of the intervention.
Endpoints:
Primary Endpoint:
The need for any anesthetic or sedative medication during MRI examination.
Secondary Endpoints:
Visual analogue scales related to fear, mood and familiarity, willingness to take part in an MRI examination again.
Study Population: 288 children aged 4-18 years who are in- or outpatients at the Pediatric Center of the Semmelweis University and are scheduled for MRI examination with anesthesia will be enrolled.
Description of Sites/Facilities Enrolling Participants:
The study takes place in the two Departments of the Pediatric Centre of the Semmelweis University
Description of Study Intervention/Experimental Manipulation:
Our research will be conducted as a three arm randomized controlled trial (VR, booklet, usual care). Participants in the VR condition are immersed in a unique 360° VR experience specifically designed for this study.
Children in the booklet condition will be prepared by using an educational booklet containing colorful illustrations about the MRI examination.
In the usual care condition children are prepared by the healthcare staff without using any specific equipment or standardized methods.
Study Duration:
36 months
Participant Duration:
All participants need a single visit intervention to complete all study related tasks.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| VR | Experimental | Participants in the VR group are immersed in a unique 360° VR experience specifically designed for this study. The custom made VR experience consists of two parts. In the first part, children find themselves in a simulated MRI room which resembles to the one they will be scanned. The second half of the VR experience introduces a mindfulness-ACT based meditation segment within the context of a space travel. |
|
| Booklet | Active Comparator | Children in the booklet condition will be prepared by using an educational booklet containing colorful illustrations of the MRI examination room and about the procedure. This serves as a resource to familiarize them with the MRI procedure, address common concerns, and provide information about what to expect during the exam. The role of the booklet condition is to serve as an active control for our experimental condition. This condition also contains an interaction with the experimenter and increases familiarity through explanation and illustrations. However, it does not involve the immersive effect of the VR. |
|
| Usual care | No Intervention | In the usual care condition children are prepared by the healthcare staff through explanations, reframing, playing as per personal preference which is currently the standard of care in our departments. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| VR | Other | The virtual environment is provided by the Oculus Quest 2 or 3 VR headset, providing a high-quality and immersive visual experience. |
|
| Measure | Description | Time Frame |
|---|---|---|
| proportion of children requiring anesthesia | proportion of children requiring any form of anesthesia or sedation during the MRI examination | during the MRI examination, assessed directly after the MRI from anesthesiology documentation |
| Measure | Description | Time Frame |
|---|---|---|
| fear | fear of the child measured on a visual analogue scale range 1-100, higher indicating increased fear | assessed directly before the intervention, directly before the MRI examination, no later than 4 hours after the MRI examination |
| mood |
| Measure | Description | Time Frame |
|---|---|---|
| fear of the parent | fear of the parent measured on a visual analogue scale, range 1-100, higher indicating increased fear | directly before the intervention, directly before the MRI examination, no later than 4 hours after the MRI examination |
| mood of the parent |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Klara Horvath, MD PhD | Contact | 0036208259395 | horvath.klara@gyerekklinika.com | |
| Sandor Erdos, MD | Contact | 036306821793 | erdos.sandor96@gmail.com |
| Name | Affiliation | Role |
|---|---|---|
| Klara Horvath, MD PhD | Semmelweis University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Pediatric Center, Semmelweis University | Recruiting | Budapest | Budapest | 1094 | Hungary |
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Participants cannot be blinded due to the nature of the study. The radiologists, anesthesiology team, MRI staff and the second research assistant administering post-procedure questionnaires and coding anesthesiology data intended to be blinded, however, children may disclose their group by talking about their experience.
| Booklet | Other | Children in the booklet condition will be prepared by using an educational booklet containing colorful illustrations of the MRI examination room and about the procedure. |
|
mood of the child measured on a visual analogue scale, scale range 1-100, higher indicating better mood
| directly before the intervention, directly before the MRI examination, no later than 4 hours after the MRI examination |
| nervousness | nervousness of the child measured on a visual analogue scale, scale range 1-100, higher increased nervousness | directly before the intervention, directly before the MRI examination, no later than 4 hours after the MRI examination |
| familiarity | familiarity of the child with the MRI examination measured on a visual analogue scale scale range 1-100, higher indicating increased familiarity with the MRI | directly before the intervention, directly before the MRI examination, no later than 4 hours after the MRI examination |
| willingness to take part again | willingness of the child to take part in a future MRI examination measured on a visual analogue scale, scale range 1-100, higher indicating more willingness taking part in a future MRI examination | no later than 4 hours after the MRI examination |
| helpfulness | indication how much the child found the preparation method helpful, measured on a visual analogue scale, scale range 1-100, higher indicating the preparation method was more helpful | directly before the MRI examination |
mood of the parent measured on a visual analogue scale, scale range 1-100, higher indicating better mood |
| directly before the intervention, directly before the MRI examination, no later than 4 hours after the MRI examination |
| nervousness of the parent | nervousness of the parent measured on a visual analogue scale, scale range 1-100, higher increased nervousness | directly before the intervention, directly before the MRI examination, no later than 4 hours after the MRI examination |
| familiarity of the parent | familiarity of the parent with the MRI examination measured on a visual analogue scale, scale range 1-100, higher indicating increased familiarity with the MRI | directly before the intervention, directly before the MRI examination, no later than 4 hours after the MRI examination |
| fear of the child assessed by parent | fear of the child assessed by parent measured on a visual analogue scale, range 1-100, higher indicating increased fear | directly before the intervention, directly before the MRI examination, no later than 4 hours after the MRI examination |
| mood of the child assessed by parent | mood of the child assessed by parent measured on a visual analogue scale, scale range 1-100, higher indicating better mood | directly before the intervention, directly before the MRI examination, no later than 4 hours after the MRI examination |
| nervousness of the child assessed by parent | nervousness of the child assessed by parent measured on a visual analogue scale, scale range 1-100, higher increased nervousness | directly before the intervention, directly before the MRI examination, no later than 4 hours after the MRI examination |
| familiarity of the child assessed by parent | familiarity of the child with the MRI examination assessed by parent measured on a visual analogue scale, scale range 1-100, higher indicating increased familiarity with the MRI | directly before the intervention, directly before the MRI examination, no later than 4 hours after the MRI examination |
| propofol dose | Dose of propofol used per body weight and duration of MRI examination. | during the MRI examination, assessed from anesthesiology documentation 1 day after the MRI at the latest |