NCT04665193

Brief Summary

The primary objective of this pilot study is to determine the feasibility and effectiveness of a COVID-19 screening program for passengers departing from YVR. This research study is conducted by The University of British Columbia (UBC) and Providence Health Care, sponsored by WestJet and Vancouver Airport Authority. The experimental study investigates point-of-care rapid test device for detecting SARS-CoV-2, the virus responsible for COVID-19. The study is investigating a method of rapid-testing for COVID-19 and will help inform the safest and most efficient way of testing departing passengers prior to security screening at Vancouver International Airport (YVR). This study is also evaluating a new passenger management system.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
592

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Nov 2020

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 23, 2020

Completed
15 days until next milestone

First Submitted

Initial submission to the registry

December 8, 2020

Completed
3 days until next milestone

First Posted

Study publicly available on registry

December 11, 2020

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 28, 2021

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 28, 2021

Completed
Last Updated

May 4, 2021

Status Verified

April 1, 2021

Enrollment Period

3 months

First QC Date

December 8, 2020

Last Update Submit

April 29, 2021

Conditions

Outcome Measures

Primary Outcomes (1)

  • COVID-19 status

    positive or negative screening result

    15 minutes

Study Arms (1)

Abbott Panbio test device

EXPERIMENTAL

WestJet passengers departing from YVR screened for COVID-19 using Abbott Panbio test device

Diagnostic Test: Rapid Antigen Test

Interventions

Rapid Antigen TestDIAGNOSTIC_TEST

Antigen Technology Lab-based test and Point of care test

Also known as: Abbott Rapid Diagnostics Panbio Covid-19 Ag Rapid Test Device (Nasopharyngeal)
Abbott Panbio test device

Eligibility Criteria

Age13 Years - 90 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • The subject must be between 19 and 80 years of age.
  • The subject must be a resident of B.C.
  • The subject must have a ticket to board a WestJet flight departing from Vancouver International Airport (YVR).
  • Have a minimum of 75 minutes of free time prior to the scheduled flight's departure.
  • Subject has access to accommodation in Canada for safe-isolation as per public health guidelines
  • Between the ages of 13 - 90
  • Travelling on any WestJet or KLM flight
  • Have a minimum of 70 minutes (if travelling within Canada) or 90 minutes (if travelling International) of free time prior to the schedule flight's departure
  • \-----------------------------------

You may not qualify if:

  • Subjects who have previously tested positive for COVID-19 within the past 90 days
  • Subjects who cannot provide written informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Vancouver International Airport, WestJet Domestic Terminal, Level 3

Richmond, British Columbia, V7B 0A4, Canada

Location

MeSH Terms

Conditions

Asymptomatic Diseases

Condition Hierarchy (Ancestors)

Disease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Don Sin, MD

    University of British Columbia

    PRINCIPAL INVESTIGATOR
  • Marc Romney, MD

    University of British Columbia

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SCREENING
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

December 8, 2020

First Posted

December 11, 2020

Study Start

November 23, 2020

Primary Completion

February 28, 2021

Study Completion

April 28, 2021

Last Updated

May 4, 2021

Record last verified: 2021-04

Data Sharing

IPD Sharing
Will not share

Locations