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Virtual Reality During Pediatric Cast Removal

A Randomized Control Trial of Virtual Reality to Reduce Anxiety During Pediatric Cast Removal

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03903510
Enrollment
184
Registered
2019-04-04
Start date
2019-05-21
Completion date
2021-09-30
Last updated
2021-02-11

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

Conditions

Fractures, Bone

Keywords

Virtual Reality, Cast removal, Fracture

Brief summary

This study is a randomized control trial of Virtual Reality during cast removal procedures at a pediatric tertiary care center.

Detailed description

Cast removal is a common outpatient procedure and is a source of pain and anxiety for children. Children are often frightened by the appearance and the noise of the saw. Additionally, the saw blade can become warm, and this can be uncomfortable. Multiple methods have been used and studied to try to make this experience easier for children. These methods include: soft music, therapeutic play, and headphones. Virtual reality (VR) devices are now increasingly affordable and portable. VR could be a way to distract children from the appearance and sound of the procedure. VR has been used in other clinical settings to help patients with the anxiety associated with medical procedures. The investigators propose a randomized trial to assess the responses (e.g. questionnaires and monitors) of children to cast removal with VR versus the standard noise reduction headphones.

Interventions

Participants in the experimental group will receive an AppliedVR virtual reality headset during their cast removal.

Sponsors

Gillette Children's Specialty Healthcare
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
4 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

* Sustained a fracture in their arm/leg * No previous experience with a cast removal * Must have at least one wrist free of immobilization (for heart rate monitor) * Parents and patient are English speaking

Exclusion criteria

* Patients with a history of epilepsy, ventricular shunt, motion sickness * Patients with any history of cognitive, visual or hearing impairment

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline heart rate during cast removal procedureHeart rate will be measured during the cast removal procedure. As this is a single visit study, heart rate will not be measured at any other time periods throughout the study.The change from baseline heart rate during cast removal procedure obtained by using an electronic monitoring wristband and measuring heart rate 15 seconds prior to and continuously during the cast removal procedure.

Secondary

MeasureTime frameDescription
Change in Patient Reported Wong-Baker FACES Pain Scale RatingThe Wong-Baker FACES Pain Scale assessment will be collected 1 minute prior to and immediately after cast removal.This is a single visit study and the assessment will not be measured at any other time periods.Patient reported pain scale that is rated on a scale of 0 (minimum) to 10 (maximum), where a higher number indicates increased pain.
Visual Analog Scale (VAS): Parental anxiety during cast removalThe VAS anxiety assessment will be performed immediately after the cast removal procedure, which is expected to last 5-10 minutes.This is a single visit study and the assessment will not be measured at any other time periods.Parental anxiety will be self reported using a 0 (minimum) to 100 (maximum) scale, where a higher number indicates increased anxiety.
Visual Analog Scale (VAS): Patient anxiety during cast removalThe VAS anxiety assessment will be performed immediately after the cast removal procedure, which is expected to last 5-10 minutes.This is a single visit study and the assessment will not be measured at any other time periods.Patient anxiety regarding the cast removal will be self reported using a 0 (minimum) to 100 (maximum) scale, where a higher number indicates increased anxiety.
Change in Parent Reported Wong-Baker FACES Pain Scale RatingThe Wong-Baker FACES Pain Scale assessment will be collected 1 minute prior to and immediately after cast removal.This is a single visit study and the assessment will not be measured at any other time periods.Parent reported pain scale that is rated from 0 (minimum) to 10 (maximum), where a higher number indicates increased pain.
Visual Analog Scale (VAS): Parental Assessment of PleasantnessThe VAS parental satisfaction assessment will be performed immediately after the cast removal procedure, which is expected to last 5-10 minutes.This is a single visit study and the assessment will not be measured at any other time periods.Parental report of how pleasant the cast removal was. Self reported using a 0 (minimum) to 100 (maximum) scale, where a higher number indicates increased pleasantness.
Visual Analog Scale (VAS): Parent Reported Worst Pain During TreatmentThe VAS parental worst pain assessment will be performed immediately after the cast removal procedure, which is expected to last 5-10 minutes.This is a single visit study and the assessment will not be measured at any other time periods.Parental report of the highest level of pain experienced by the child during the cast removal. Reported using a 0 (minimum) to 100 (maximum) scale, where a higher number indicates increased pain.
Visual Analog Scale (VAS): Patient Reported Worst Pain During TreatmentThe VAS patient worst pain assessment will be performed immediately after the cast removal procedure, which is expected to last 5-10 minutes.This is a single visit study and the assessment will not be measured at any other time periods.Patient report of the highest level of pain experienced by the child during the cast removal. Reported using a 0 (minimum) to 100 (maximum) scale, where a higher number indicates increased pain.
Visual Analog Scale (VAS): Parental SatisfactionThe VAS parental satisfaction assessment will be performed immediately after the cast removal procedure, which is expected to last 5-10 minutes.This is a single visit study and the assessment will not be measured at any other time periods.Parental satisfaction regarding the cast removal will be self reported using a 0 (minimum) to 100 (maximum) scale, where a higher number indicates increased satisfaction.

Countries

United States

Contacts

Primary ContactAndrew G Georgiadis, MD
andrewgeorgiadis@gillettechildrens.com651-602-3262
Backup ContactChristine K Santa Ana, BS
ChristineKSantaAna@gillettechildrens.com651-229-1763

Outcome results

None listed

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