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Clinical Trials/NCT03681730
NCT03681730
Unknown
Not Applicable

A Pragmatic Randomized Controlled Trial of Virtual Reality vs Standard-of-Care for Comfort During Intravenous Catheterization

University of British Columbia1 site in 1 country64 target enrollmentMay 2, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Intravenous Catheterization
Sponsor
University of British Columbia
Enrollment
64
Locations
1
Primary Endpoint
Pain using the Faces Pain Scale - Revised.
Last Updated
7 years ago

Overview

Brief Summary

Children often need an intravenous catheter placement for delivery of fluids and medications, a procedure associated with pain and anxiety. In the Emergency Department topical anesthetics are frequently used.

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 topical anaesthetics during IV placement procedure. Investigators will measure pain, anxiety and satisfaction, amount of analgesics used and the level of success in placing the IV and compare between the two groups.

Registry
clinicaltrials.gov
Start Date
May 2, 2018
End Date
May 1, 2019
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ran Goldman

Professor and Co-head of the Division of Clinical Pharmacology, Division of Emergency Medicine, Department of Pediatrics; Investigator, BC Children's Hospital

University of British Columbia

Eligibility Criteria

Inclusion Criteria

  • Children age 6 - \<17
  • The managing physician determines a need for an intravenous catheterization (IV) procedure
  • 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, autism, others)
  • Triage Category 1 (resuscitation)
  • Facial features or injury prohibiting wearing the VR goggles

Outcomes

Primary Outcomes

Pain using the Faces Pain Scale - Revised.

Time Frame: Pain is reported by children immediately following completion of the IV start

Level of pain as reported by children using Faces Pain Scale - Revised. The scale includes six faces that represent progressively more intense features of pain. Children point to the face that best represents their current level of pain. The minimum score is 0 (representing least pain) and the maximum score is 10 (representing greater pain). The scale increase in increments of 2.

Secondary Outcomes

  • Patient Satisfaction determined by Global Rating Scale(Satisfaction questions are reported by children immediately following completion of the IV start)
  • Parent Satisfaction determined qualitatively by an open ended question(Satisfaction question is reported by parents immediately following completion of the IV start)
  • Number of IV Trials Until Success(This number will be collected during the procedure)
  • Anxiety using the Venham Situational Anxiety Score(Anxiety is reported by children immediately following completion of the IV start)
  • Patient Satisfaction determined qualitatively by an open ended question(Satisfaction questions are reported by children immediately following completion of the IV start)
  • Medication Dose(These will be recorded during the procedure and immediately following the procedure using the patient chart and nursing notes)
  • Timing(Documented immediately after patient and family given discharge paperwork)

Study Sites (1)

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