- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07102472
- Original Trial
An Experiment Comparing Public Reactions to the Labels "Community Immunity" Versus "Herd Immunity".
July 28, 2025 updated by: Laval University
Community Immunity Versus Herd Immunity
Participants are shown a scenario consisting of static images from a previous study ("herdimm") showing a visualization of how herd immunity works.
Participants are randomized to see the text with the term "herd immunity" or "community immunity."
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
350
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Holly Witteman, PhD
- Phone Number: 418-656-2131
- Email: holly.witteman@fmed.ulaval.ca
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Able to use a computer
- Able to use the internet
- Able to read and respond to questions in English or French
- 18+ years old and living in Canada
Exclusion Criteria:
- Unable to view images on a computer
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Placebo Comparator: Herd immunity
|
Using the traditional term "herd immunity"
|
|
Experimental: Community immunity
|
In the intervention arm, participants are shown the less traditional term "community immunity" in place of the more traditional "herd immunity"
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Orientation towards protection of others
Time Frame: Immediately after the intervention
|
A measure of the extent to which people believe that individual vaccination behavior is important to protect others.
Question wording: "When a safe and effective vaccine exists that can prevent people from catching and passing on a contagious disease, it is important for people to get vaccinated to protect ..." Measured across two to three items (family, others in the community, people who are more vulnerable to disease) on a 7-point Likert-type scale (strongly disagree = 1, strongly agree = 7).
|
Immediately after the intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
July 22, 2025
Primary Completion (Estimated)
August 31, 2025
Study Completion (Estimated)
August 31, 2025
Study Registration Dates
First Submitted
July 28, 2025
First Submitted That Met QC Criteria
July 28, 2025
First Posted (Actual)
August 3, 2025
Study Record Updates
Last Update Posted (Actual)
August 3, 2025
Last Update Submitted That Met QC Criteria
July 28, 2025
Last Verified
July 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- commimm
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Anonymized data will be deposited on Borealis, Laval University's official data repository.
IPD Sharing Time Frame
IPD and supporting information will be available when the study report is complete.
IPD Sharing Access Criteria
Anyone with internet access will be able to access the public-facing file.
Some data may require access through Borealis registration.
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- ICF
- ANALYTIC_CODE
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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