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Virtual Reality vs. Standard-of-Care for Comfort During Laceration Repair

University of British Columbia logo

University of British Columbia

Status

Unknown

Conditions

Laceration

Treatments

Device: Virtual Reality

Study type

Interventional

Funder types

Other

Identifiers

NCT03681717
H17-02711

Details and patient eligibility

About

Lacerations are a common reason for presentation to the Emergency Department and children needing laceration repair with sutures are experiencing pain and anxiety.

Virtual Reality (VR) is an immersive experience using sight, sound, and position sense. Using VR may enhance distraction during the painful procedure and may reduce attention to pain.

This study will randomize children (6 - 16 years old) to receive Virtual Reality or standard of care in addition to pharmacoanalgesia during a laceration repair procedure. Investigators will measure pain, anxiety, satisfaction, amount of analgesia and the length of procedure and compare between the two groups.

Enrollment

64 estimated patients

Sex

All

Ages

6 to 16 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Children age 6 - <17 years
  • Arriving to the Emergency Department with a chief complaint of laceration
  • The managing physician determines need for repair with suture
  • Parents will sign a consent form and children will sign an assent form

Exclusion criteria

  • Children with conditions that may prohibit participation or evaluation of the procedure (such as developmental delay)
  • Triage category 1 (resuscitation)
  • Facial features or injury prohibiting wearing VR goggles

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

64 participants in 2 patient groups

Virtual Reality
Experimental group
Description:
Participants are distracted by wearing the virtual reality headset and watching a roller coaster app during laceration repair with sutures.
Treatment:
Device: Virtual Reality
Control (Standard-of-Care)
No Intervention group
Description:
Participants are distracted with Standard-of-Care by doctors, nurses, nurse practitioners, child life specialists and/or parents.

Trial contacts and locations

1

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Central trial contact

Ran D. Goldman, MD

Data sourced from clinicaltrials.gov

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