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Vaccine Norms Feedback for Vaccine Hesitancy
N/A
Recruiting
Led By Scott Graupensperger, PhD
Research Sponsored by University of Washington
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, an average of 6 months
Awards & highlights
No Placebo-Only Group
Summary
This trial will use an online intervention to correct misperceived social norms related to vaccine hesitancy among young adults (18-25) in order to increase uptake & reduce time to first dose of the COVID-19 vaccine.
Who is the study for?
This trial is for young adults aged 18-24 in the US who haven't had a COVID-19 vaccine and are willing to participate. They must understand English well, pass attention checks during screening, and give their consent to be part of the study.
What is being tested?
The study tests an online intervention giving personalized feedback based on social norms to reduce vaccine hesitancy among young adults. Participants will be randomly assigned to receive this intervention or an attention-matched control, with follow-ups over six months.
What are the potential side effects?
Since this trial involves no medical treatments but rather informational feedback, there are no direct physical side effects expected from participating in the study.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through study completion, an average of 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, an average of 6 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
COVID-19 vaccine attitudes
COVID-19 vaccine uptake
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Vaccine Norms FeedbackExperimental Treatment1 Intervention
The participants in the treatment condition will receive personalized normative feedback (PNF) that entails correcting normative misperceptions for US young adults' vaccine uptake rates and prevalence of vaccine hesitancies (e.g., fear of side effects). Participants will be shown discrepancies between their perceived estimate of young adults' vaccination rates and actual national estimates derived from the US Census Bureau's Household Pulse Survey to highlight, in most cases, that they underestimated the vaccination norms.
Group II: Alcohol Norms FeedbackActive Control1 Intervention
Participants randomized to control will complete all measures at the same time as participants in the treatment condition, but will not receive any normative information regarding vaccines. Instead, to match for attention and provide potential benefit, those in the control condition will receive a standard dynamic norms feedback pertaining to alcohol use norms and behaviors.
Find a Location
Who is running the clinical trial?
University of WashingtonLead Sponsor
1,831 Previous Clinical Trials
1,906,969 Total Patients Enrolled
Centers for Disease Control and PreventionFED
892 Previous Clinical Trials
22,000,162 Total Patients Enrolled
Scott Graupensperger, PhDPrincipal InvestigatorUniversity of Washington
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am not willing to participate in the trial.I am between 18 and 24 years old.I have not received a COVID-19 vaccine.I am not fluent in English.
Research Study Groups:
This trial has the following groups:- Group 1: Vaccine Norms Feedback
- Group 2: Alcohol Norms Feedback
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.