Messaging Strategies to Increase Peer Education on COVID-19 Vaccination and Climate Change

Developing and Evaluating Messaging Strategies to Increase Peer Education About COVID-19 Vaccination and Climate Change Among Adults in the United States

The primary objective of this protocol is to develop and evaluate peer communication interventions to encourage peer education around COVID-19 vaccination and climate change.

Study Overview

Status

Completed

Detailed Description

Investigators will use a RCT peer education intervention to address climate change-related behaviors as a control condition for the vaccination intervention. Both issues represent serious public health priorities and are sufficiently unrelated in order to act as control conditions for each other.

As a control topic, investigators will address climate change communication. This parallel topic was selected because it is (1) reasonably unrelated to the COVID-19 condition, (2) has clear individual-level behaviors that can be targeted for intervention, (3) has diversity in public attitudes like COVID-19 vaccines,18 (4) has parallels in COVID-19 in terms of polarization and discrediting of scientific research, (5) represents a significant threat to population health, and (6) has significant racial and ethnic disparities paralleling those of COVID-19.

Investigators will recruit a second sample of up to 800 eligible participants who will be asked to complete an intervention session, where they will receive training on how to talk to members of their social network about either COVID-19 vaccination or climate change. The two intervention conditions will differ based on topic (vaccination/climate change) but the intervention components will be comparable. During the intervention, participants will watch a series of videos that teach key communication skills for having conversation about the assigned topic. Additional videos will provide training in how to use social media as a communication platform to share information in case participants are unfamiliar. Participants will then complete practice activities where they will construct hypothetical conversations and react to/critique example conversations to practice implementing the communication skills. Upon completing the intervention, participants will be asked to try to talk to others in their social network about the topic area they were assigned to.

Two to four weeks after the intervention, participants who completed the intervention will be asked to complete a follow-up survey to assess whether participants had conversations with others in their social networks, if they used social media/text/e-mail to share accurate information, and to understand the outcome of the conversations (i.e. did they result in behavior change).

Study Type

Interventional

Enrollment (Actual)

600

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

Study Locations

    • Maryland
      • Baltimore, Maryland, United States, 21205
        • Johns Hopkins Bloomberg School of Public Health

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • English-speaking
  • English-reading
  • Reside in the United States
  • Over 18 years of age
  • Have passed Prolific's data quality checks on their previously submitted work
  • Have heard of COVID-19 and the COVID-19 vaccine

Exclusion Criteria:

  • Do not provide informed consent.

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: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: vaccine
Promotes COVID-19 vaccine uptake
training in communication skills
Active Comparator: climate change
Promotes climate change activism
training in communication skills

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Frequency of conversations about vaccines
Time Frame: 1 month
A brief measure of frequency of conversations about vaccines in the prior month
1 month
Frequency of conversations about climate change
Time Frame: 1 month
A brief measure of frequency of conversations about climate in the prior month
1 month
Actions to promote vaccine uptake in social network
Time Frame: 1 month
Number of social network members that participate encouraged to become vaccinated
1 month
Actions to promote climate change activism in social network
Time Frame: 1 month
Number of social network members that participate encouraged to engage in climate change actions
1 month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Carl A Latkin, Ph.D., Johns Hopkins Bloomberg School of Public Health

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 (Actual)

August 30, 2022

Primary Completion (Actual)

December 20, 2022

Study Completion (Actual)

January 20, 2024

Study Registration Dates

First Submitted

August 31, 2022

First Submitted That Met QC Criteria

September 2, 2022

First Posted (Actual)

September 7, 2022

Study Record Updates

Last Update Posted (Actual)

January 24, 2024

Last Update Submitted That Met QC Criteria

January 23, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • IRB00018956

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

unidentified data

IPD Sharing Time Frame

Two years from the end of the study.

IPD Sharing Access Criteria

contact the PI.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • ICF

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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