An Evaluation of a Dynamic Web-Based Visualization of Community Immunity
1 other identifier
interventional
5,516
1 country
1
Brief Summary
This study is a PhD project conducted by Ms. Hina Hakim, supervised by Dr. Holly O. Witteman, PhD, and co-supervised Dr. Daniel Reinharz, professors and researchers at the Faculty of Medicine at Laval University. The purpose of this study is to evaluate the effects of visualization conveying the concept of community immunity or herd immunity on risk perception (towards individual, family, community and vulnerable people in communities) (primary outcome) and on emotions, attitudes, knowledge, and behavioural intentions (secondary outcomes).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Mar 2021
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2021
CompletedFirst Submitted
Initial submission to the registry
March 4, 2021
CompletedFirst Posted
Study publicly available on registry
March 9, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2021
CompletedAugust 29, 2024
August 1, 2024
4 months
March 4, 2021
August 27, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Risk perception
6 items assessing risk perception (item 1 = risk perception as comprehension, scale 0-100, higher numbers better; items 2-5 = risk perception as feelings, scale 1-7, higher numbers better; complete list of items and response wording available in uploaded questionnaire herdimm\_phase3\_questionnaire\_2021-03-01.pdf)
immediately after intervention or control
Secondary Outcomes (5)
Emotions
immediately after intervention or control
Knowledge
immediately after intervention or control
Trust in information
immediately after intervention or control
Vaccination intentions
immediately after intervention or control
5C scale
immediately after intervention or control
Study Arms (13)
controlgeneric
NO INTERVENTIONNo intervention provided. Participant answers outcome questions about an unnamed vaccine-preventable disease. English and French.
controlmeasles
NO INTERVENTIONNo intervention provided. Participant answers outcome questions about measles. English and French.
controlpertussis
NO INTERVENTIONNo intervention provided. Participant answers outcome questions about pertussis. English and French.
controlflu
NO INTERVENTIONNo intervention provided. Participant answers outcome questions about flu. English and French.
herdimmgeneric
EXPERIMENTALWeb-based application (main intervention) provided. Participant answers outcome questions about an unnamed vaccine-preventable disease. English and French.
herdimmmeasles
EXPERIMENTALWeb-based application (main intervention) provided. Participant answers outcome questions about measles. English and French.
herdimmpertussis
EXPERIMENTALWeb-based application (main intervention) provided. Participant answers outcome questions about pertussis. English and French.
herdimmflu
EXPERIMENTALWeb-based application (main intervention) provided. Participant answers outcome questions about flu. English and French.
robertkochgeneric
ACTIVE COMPARATORWeb-based application (comparator) provided. Participant answers outcome questions about an unnamed vaccine-preventable disease. English only.
sbsnewsgeneric
ACTIVE COMPARATORVideo (comparator) provided. Participant answers outcome questions about an unnamed vaccine-preventable disease. English only.
guardianmeasles
ACTIVE COMPARATORVideo (comparator) provided. Participant answers outcome questions about measles. English only.
theotheredmundmeasles
ACTIVE COMPARATORVideo (comparator) provided. Participant answers outcome questions about measles. English only.
publichealthagencycanadaflu
ACTIVE COMPARATORVideo (comparator) provided. Participant answers outcome questions about flu. English and French.
Interventions
In this visualization participants can build their own avatar representing themselves and 8 other avatars representing people around them, like their family or coworkers. Our visualization then uses these avatars in a brief narrated video explaining how herd immunity works.
A screen capture of an interactive visualization: https://www.theguardian.com/society/ng-interactive/2015/feb/05/-sp-watch-how-measles-outbreak-spreads-when-kids-get-vaccinated
A gif showing measles spreading through populations with differing levels of vaccine coverage: https://imgur.com/gallery/8M7q8#J7LANQ4
A video showing how herd immunity works in general: https://www.sbs.com.au/news/two-sydney-babies-too-young-to-be-vaccinated-infected-with-measles
A video showing how herd immunity works in the context of influenza: https://www.canada.ca/fr/sante-publique/services/video/la-grippe-n-en-passez-pas-les-maux.html
A web-based application showing how herd immunity works in general: http://rocs.hu-berlin.de/D3/herd/
Eligibility Criteria
You may qualify if:
- Members of the general population in Canada
- At least 18 years old
- Able to provide free and informed consent
- Able to read and understand French or English
- Able to use a computer
You may not qualify if:
- \- No internet access
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Laval Universitylead
Study Sites (1)
Université Laval
Québec, G1V 0A6, Canada
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Holly Witteman, PhD
Laval University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- INVESTIGATOR
- Masking Details
- This will be a single-blinded study because we cannot mask participants to the fact that they have been randomized to a visualization e.g., about measles. However, participants will not necessarily know the purpose of the study arm to which they are assigned,and investigators will be blinded to study arm during data analysis (investigators are not aware of whether the next eligible participant will be receiving treatment or control intervention.)
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- FACTORIAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 4, 2021
First Posted
March 9, 2021
Study Start
March 1, 2021
Primary Completion
July 1, 2021
Study Completion
July 1, 2021
Last Updated
August 29, 2024
Record last verified: 2024-08
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF, ANALYTIC CODE
- Time Frame
- As soon as possible upon completion of the study and posting of a preprint with results.
- Access Criteria
- Freely available.
Anonymized data (answers to questions in the survey including socio-demographic information) will be deposited in a public repository (Dataverse de l'Université Laval (Laval University)) which will allow data sharing with the scientific community. No information that would allow anyone to identify a person will be deposited in this public repository. Study protocol and statistical analysis plan have been deposited in Open Science Framework.