Data

The effect of enhanced messaging on COVID-19 testing intentions and behaviour dataset

University of Sydney

Dataset description

This dataset includes 1527 participants (from 18 to 39 years old, both males and females) receiving 2 audio-visual interventions addressing common COVID-19 testing barriers for people with lower health literacy. Participants were recruited from New South Wales, Australia into this randomised controlled trial. Anonymous quantitative data on outcomes for each group including the intention to undergo testing for COVID-19 if symptomatic, intentions about other prevention behaviours (self-isolation if symptomatic, social distancing of 1.5 m, washing hands regularly, and wearing masks in crowded indoor areas), understanding of messaging, risk perceptions, social stigma, and self-efficacy (ie, confidence in overcoming perceived barriers to testing) is included in this dataset. The file type is .XLS.
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Source Study

Trial acronym

Not available

Trial ID

ACTRN12621000876897

Purpose

Prevention

Phase

Not Applicable

Funding

University,Marie Bashir Institute at the University of Sydney

Scientific enquiries

Dr Carissa Bonner

Brief Summary

COVID-19 response in Australia relies on people getting tested should they experience symptoms; however, national data indicate suboptimal uptake. This study aims to improve the uptake of COVID-19 testing by addressing peoples’ specific reasons for not getting tested. We will be testing whether we can increase people's intention to get tested for COVID-19 if they symptoms using an animation, as compared to the government's written information. We will also be testing whether an animation based o ....
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Key Inclusion Criteria

Live in Australia, aged 18-39, not University educated

Key Exclusion Criteria

None

Can healthy volunteers participate?

Yes

 

Population

Sample Size    1500

Min. age    18 Years

Max. age    39 Years

Sex    Both males and females

Condition category    COVID-19

Condition code    Infection , Mental Health , Public Health , Respiratory

Intervention

Intervention code Behaviour , Prevention

This study is a survey which will be conducted online through the Qualtrics platform. Participants will be recruited on social media (Facebook on Instagram) with an advertisement with the message ‘Over 18? We want to hear from you! Complete a short survey about COVID-19 and be in with the chance to win a $20 gift card’. If they click on the advert, participants will be directed to the landing page where they can read the PIS and Consent Form before accessing the survey. The survey itself will be ....
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Comparison

Control group Active

COVID-19 testing information on Australian Government website (NSW Health COVID-19 FAQ: https://www.health.nsw.gov.au/Infectious/covid-19/Pages/frequently-asked-questions.aspx#4 ). Questions include ‘Is it safe to get tested for COVID-19?’ ‘Is COVID-19 testing painful?’ ‘Is COVID-19 testing free?’ The information is written for the control group (not a video). This control group will be compared in Hypothesis 1 against both intervention groups, and the two intervention groups will be compared ag ....
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Outcomes

Outcome: Intention to get tested for COVID-19: Over the next 4 weeks, I plan to get tested if I have COVID-19 symptoms [7 point scale from Strongly disagree to Strongly agree]
Timepoint: Immediately post-intervention

Outcome: Intention to get tested for COVID-19 as a hypothetical: Imagine you woke up with a sore throat tomorrow. Would you get tested straight away? [7 point scale from Strongly disagree to Strongly agree]
Timepoint: Immediately post-intervention

Outcome: Perceived intention for someone else to get tested for COVID-19: Most people my age would get tested after seeing this information/video. [7 point scale from Strongly disagree to Strongly agree]
Timepoint: Immediately post-intervention

Study Protocol: Study protocol
Data Dictionary: Not Available

Will individual participant data (IPD) for this trial be available?

yes

What data in particular will be shared?

Anonymous quantitative data on outcomes for each group

When will data be available?

For 2 years after all data has been collected

Available to whom?

Other researchers

Available for what types of analyses?

Quantitative analysis

Source study information is derived from the Australian New Zealand Clinical Trials Registry (ANZCTR). For more information on the ANZCTR, please see anzctr.org.au