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CATCH-UP Vaccines: Extension of Community - Engaged Approaches to Testing in Community and Healthcare Settings for Underserved Populations (COVID-19)

Primary Purpose

COVID-19, Vaccine Refusal

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Text Message
Motivational Interviewing
Electronic Educational Message with Tailored Questions/Prompts
Sponsored by
University of Oklahoma
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for COVID-19 focused on measuring COVID-19 Vaccine Hesitancy, MOST (multiphase optimization strategy)

Eligibility Criteria

18 Years - 100 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. 18 years of age and older
  2. Must be eligible to receive a COVID-19 vaccine dose at the time of consent based on the following criteria:

    1. No previous doses of a COVID-19 vaccine (Pfizer-BioNTech, Moderna, or Janssen)
    2. At least 21 days since first dose of Pfizer-BioNTech to be eligible for a second dose
    3. At least 28 days since first dose of Moderna to be eligible for a second dose
    4. For those who are severely immunocompromised, eligible for third Pfizer or Moderna dose at least 28 days after the second dose; eligible for 2nd dose Pfizer/Moderna at least 28 days after first Janssen.
    5. At least 5 months since completing the two dose Pfizer-BioNTech vaccine series or the Moderna vaccine series (for immunocompromised, at least 3 months after third dose of either of Pfizer/Moderna vaccines or 2 months after second dose if Janssen was the first dose) to be eligible for booster of any authorized COVID-19 vaccine
    6. At least 2 months since completing the Janssen single dose to be eligible for booster of any authorized COVID-19 vaccine
  3. Ability to read and speak English

Exclusion Criteria:

  1. Those who have received a third dose or booster dose of any approved COVID-19 vaccine.
  2. Those with active COVID-19 disease (either through self-report, symptoms consistent with COVID-19, or viral test at the event if available).

Sites / Locations

  • Oklahoma Clinical and Translational Science InstituteRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm 7

Arm 8

Arm Type

No Intervention

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Arm Label

Condition 1

Condition 2

Condition 3

Condition 4

Condition 5

Condition 6

Condition 7

Condition 8

Arm Description

Participants will not receive a text message notifying participants about COVID-19 vaccine availability, standard interpretation of serology SARS-CoV-2 antibody results with COVID-19 vaccination discussion, and an attention control educational message.

Participants will not receive a text message notifying participants about COVID-19 vaccine availability, standard interpretation of serology SARS-CoV-2 antibody results with COVID-19 vaccination discussion, and an educational message about COVID-19 vaccines.

Patients will not receive a text message notifying participants about COVID-19 vaccine availability, motivational interviewing about serology SARS-CoV-2 antibody results with COVID-19 vaccination discussion, and an attention control educational message.

Patients will not receive a text message notifying participants about COVID-19 vaccine availability, motivational interviewing about serology SARS-CoV-2 antibody results with vaccination discussion, and an educational message about COVID-19 vaccines.

Patients will receive a text message notifying participants about COVID-19 vaccine availability, motivational interviewing about serology SARS-CoV-2 antibody results with vaccination discussion, and an educational message about COVID-19 vaccines.

Patients will receive a text message notifying participants about COVID-19 vaccine availability, motivational interviewing about serology SARS-CoV-2 antibody results with vaccination discussion, and an attention control educational message.

Patients will receive a text message notifying participants about COVID-19 vaccine availability, standard interpretation of serology SARS-CoV-2 antibody results with COVID-19 vaccination discussion, and an attention control educational message.

Patients will receive a text message notifying participants about COVID-19 vaccine availability, standard interpretation of serology SARS-CoV-2 antibody results with COVID-19 vaccination discussion, and an educational message about COVID-19 vaccines.

Outcomes

Primary Outcome Measures

Percentage of participants who plan to receive a COVID-19 vaccine post-intervention
Investigators will measure this with the question "How likely are you to get an approved COVID-19 vaccine?" and "If you have received 1 dose of the Janssen vaccine or 2 doses of the Moderna or Pfizer vaccine, how likely are you to get an approved booster shot?" We will compare intention to receive a COVID-19 vaccine or booster among those receiving the interventions compared to those not receiving the intervention

Secondary Outcome Measures

Percentage of participants who self-report COVID-19 vaccine uptake
The secondary outcome will be vaccine uptake, including self-report of receiving an initial dose of any approved vaccine, two doses of Pfizer or Moderna vaccines, or a booster of any approved vaccine.

Full Information

First Posted
February 1, 2022
Last Updated
August 29, 2022
Sponsor
University of Oklahoma
Collaborators
National Institutes of Health (NIH), National Institute of General Medical Sciences (NIGMS)
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1. Study Identification

Unique Protocol Identification Number
NCT05236270
Brief Title
CATCH-UP Vaccines: Extension of Community - Engaged Approaches to Testing in Community and Healthcare Settings for Underserved Populations (COVID-19)
Official Title
CATCH-UP Vaccines: Extension of Community - Engaged Approaches to Testing in Community and Healthcare Settings for Underserved Populations
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 25, 2022 (Actual)
Primary Completion Date
July 2023 (Anticipated)
Study Completion Date
September 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Oklahoma
Collaborators
National Institutes of Health (NIH), National Institute of General Medical Sciences (NIGMS)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Oklahoma has high COVID-19 incidence, particularly among underserved minority and rural Oklahomans. Oklahoman's are also reporting SARS-CoV-2 vaccine hesitancy and signs of slowing vaccine uptake, with increased hesitancy among American Indian and rural populations. The project aims to work with ongoing community testing events to implement interventions to improve vaccine uptake among Oklahoma's underserved populations.
Detailed Description
This proposal unites academic and community partners to solve a dire need for SARS-CoV-2 vaccine uptake in rural, underserved minority, and at-risk populations. Oklahoma has high COVID-19 incidence, high vaccine hesitancy, and signs of a slowing SARS-CoV-2 vaccine uptake. Oklahoma's cumulative incidence is higher in rural compared to urban counties. AI people have a higher incidence of COVID-19 compared to white populations in Oklahoma. Despite high incidence, as of April 2021, an estimated 54% of Oklahomans who have not yet been vaccinated reported unwillingness to receive the SARS-CoV-2 vaccine. Vaccine hesitancy was even greater in AI people (62%). The most commonly reported concerns are vaccine side effects and safety (30%). Despite early progress in disseminating vaccines in Oklahoma, all signs point to waning interest in receiving a vaccine, with many vaccine clinics unable to fill all available slots, particularly in tribal clinics and rural areas. This proposal is an extension of the Oklahoma Shared Clinical Translational Resources (OSCTR) project CATCH-UP (Community-engaged Approaches to Testing in Community and Healthcare settings for Underserved Populations) in partnership with community organizations who work with underserved minority and rural populations. This project will build on existing strengths and infrastructure to improve SARS-CoV-2 vaccine uptake in these highly susceptible populations. The goal of the project is to pilot interventions to improve awareness and uptake of COVID-19 vaccination. The project aims to work with CATCH-UP community events to implement interventions to improve vaccine uptake among Oklahoma's underserved populations. To do so, the proposed study employs a multiphase optimization strategy (MOST). The proposed study uses the preparation and optimization phases of the MOST framework across the following aims: 1) Identify SARS-CoV-2 vaccination barriers/facilitators and assess acceptability and feasibility of a suite of evidence-based vaccine intervention strategies among Oklahoma's rural, minority, and high-risk populations to inform a targeted multicomponent intervention; and 2) Develop and optimize a multicomponent intervention to improve SARS-CoV-2 vaccination among Oklahoman's seeking SARS-CoV-2 testing at CATCH-UP testing events. Investigators will conduct a pilot of these interventions based on community input, which will be evaluated for inclusion in a future, full-scale implementation study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COVID-19, Vaccine Refusal
Keywords
COVID-19 Vaccine Hesitancy, MOST (multiphase optimization strategy)

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Model Description
Interventions will address three primary areas to improve vaccination uptake: (1) process (text messages); (2) teachable moment messaging (motivational interviewing); and (3) barrier elicitation and reduction (electronic survey with tailored questions/prompts). In a factorial research design, two or more independent variables are concurrently examined within the same trial. The three factors are crossed with one another to create a total of eight experimental conditions. An equal number of sites are randomly assigned to each condition, using a random number generator.
Masking
InvestigatorOutcomes Assessor
Masking Description
Investigators who are providing the intervention and conducting analysis will be masked to study assignment
Allocation
Randomized
Enrollment
2000 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Condition 1
Arm Type
No Intervention
Arm Description
Participants will not receive a text message notifying participants about COVID-19 vaccine availability, standard interpretation of serology SARS-CoV-2 antibody results with COVID-19 vaccination discussion, and an attention control educational message.
Arm Title
Condition 2
Arm Type
Experimental
Arm Description
Participants will not receive a text message notifying participants about COVID-19 vaccine availability, standard interpretation of serology SARS-CoV-2 antibody results with COVID-19 vaccination discussion, and an educational message about COVID-19 vaccines.
Arm Title
Condition 3
Arm Type
Experimental
Arm Description
Patients will not receive a text message notifying participants about COVID-19 vaccine availability, motivational interviewing about serology SARS-CoV-2 antibody results with COVID-19 vaccination discussion, and an attention control educational message.
Arm Title
Condition 4
Arm Type
Experimental
Arm Description
Patients will not receive a text message notifying participants about COVID-19 vaccine availability, motivational interviewing about serology SARS-CoV-2 antibody results with vaccination discussion, and an educational message about COVID-19 vaccines.
Arm Title
Condition 5
Arm Type
Experimental
Arm Description
Patients will receive a text message notifying participants about COVID-19 vaccine availability, motivational interviewing about serology SARS-CoV-2 antibody results with vaccination discussion, and an educational message about COVID-19 vaccines.
Arm Title
Condition 6
Arm Type
Experimental
Arm Description
Patients will receive a text message notifying participants about COVID-19 vaccine availability, motivational interviewing about serology SARS-CoV-2 antibody results with vaccination discussion, and an attention control educational message.
Arm Title
Condition 7
Arm Type
Experimental
Arm Description
Patients will receive a text message notifying participants about COVID-19 vaccine availability, standard interpretation of serology SARS-CoV-2 antibody results with COVID-19 vaccination discussion, and an attention control educational message.
Arm Title
Condition 8
Arm Type
Experimental
Arm Description
Patients will receive a text message notifying participants about COVID-19 vaccine availability, standard interpretation of serology SARS-CoV-2 antibody results with COVID-19 vaccination discussion, and an educational message about COVID-19 vaccines.
Intervention Type
Behavioral
Intervention Name(s)
Text Message
Intervention Description
Participants will be randomized to receive or not receive a text message encouraging COVID-19 vaccine uptake.
Intervention Type
Behavioral
Intervention Name(s)
Motivational Interviewing
Intervention Description
Participants will be randomized to receive either motivational interviewing when receiving SARS-CoV-2 antibody test results or standard interpretation of antibody results.
Intervention Type
Behavioral
Intervention Name(s)
Electronic Educational Message with Tailored Questions/Prompts
Intervention Description
Participants will be randomized to receive either an electronic educational message tailored to their COVID-19 vaccine concerns and vaccine status or an attention control message about overall healthy choices.
Primary Outcome Measure Information:
Title
Percentage of participants who plan to receive a COVID-19 vaccine post-intervention
Description
Investigators will measure this with the question "How likely are you to get an approved COVID-19 vaccine?" and "If you have received 1 dose of the Janssen vaccine or 2 doses of the Moderna or Pfizer vaccine, how likely are you to get an approved booster shot?" We will compare intention to receive a COVID-19 vaccine or booster among those receiving the interventions compared to those not receiving the intervention
Time Frame
Baseline to Month 2
Secondary Outcome Measure Information:
Title
Percentage of participants who self-report COVID-19 vaccine uptake
Description
The secondary outcome will be vaccine uptake, including self-report of receiving an initial dose of any approved vaccine, two doses of Pfizer or Moderna vaccines, or a booster of any approved vaccine.
Time Frame
Baseline to Month 2

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 18 years of age and older Must be eligible to receive a COVID-19 vaccine dose at the time of consent based on the following criteria: No previous doses of a COVID-19 vaccine (Pfizer-BioNTech, Moderna, or Janssen) At least 21 days since first dose of Pfizer-BioNTech to be eligible for a second dose At least 28 days since first dose of Moderna to be eligible for a second dose For those who are severely immunocompromised, eligible for third Pfizer or Moderna dose at least 28 days after the second dose; eligible for 2nd dose Pfizer/Moderna at least 28 days after first Janssen. At least 5 months since completing the two dose Pfizer-BioNTech vaccine series or the Moderna vaccine series (for immunocompromised, at least 3 months after third dose of either of Pfizer/Moderna vaccines or 2 months after second dose if Janssen was the first dose) to be eligible for booster of any authorized COVID-19 vaccine At least 2 months since completing the Janssen single dose to be eligible for booster of any authorized COVID-19 vaccine Ability to read and speak English Exclusion Criteria: Those who have received a third dose or booster dose of any approved COVID-19 vaccine. Those with active COVID-19 disease (either through self-report, symptoms consistent with COVID-19, or viral test at the event if available).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Amanda E Janitz, PhD
Phone
405-271-2229
Ext
48081
Email
Amanda-Janitz@ouhsc.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Timothy M VanWagoner, PhD
Phone
405-271-3480
Email
Timothy-VanWagoner@ouhsc.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Judith A James, MD, PhD
Organizational Affiliation
University of Oklahoma
Official's Role
Principal Investigator
Facility Information:
Facility Name
Oklahoma Clinical and Translational Science Institute
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73104
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Amanda E Janitz, PhD
Phone
405-271-2229
Ext
48081
Email
Amanda-Janitz@ouhsc.edu
First Name & Middle Initial & Last Name & Degree
Timothy M VanWagoner, PhD
Phone
405-271-3480
Email
Timothy-VanWagoner@ouhsc.edu
First Name & Middle Initial & Last Name & Degree
Judith A James, MD, PhD

12. IPD Sharing Statement

Citations:
PubMed Identifier
19664226
Citation
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Results Reference
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PubMed Identifier
31274411
Citation
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Results Reference
background
PubMed Identifier
29734944
Citation
Garbutt JM, Dodd S, Walling E, Lee AA, Kulka K, Lobb R. Barriers and facilitators to HPV vaccination in primary care practices: a mixed methods study using the Consolidated Framework for Implementation Research. BMC Fam Pract. 2018 May 7;19(1):53. doi: 10.1186/s12875-018-0750-5.
Results Reference
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PubMed Identifier
26890168
Citation
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Results Reference
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PubMed Identifier
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Citation
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Results Reference
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PubMed Identifier
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Citation
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Results Reference
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Links:
URL
https://covid.cdc.gov/covid-data-tracker/
Description
COVID Data Tracker
URL
https://obssr.od.nih.gov/wp-content/uploads/2020/12/COVIDReport_Final.pdf
Description
COVID-19 Vaccination Communication: Applying Behavioral and Social Science to Address Vaccine Hesitancy and Foster Vaccine Confidence
URL
https://www.kff.org/disparities-policy/issue-brief/low-income-and-communities-of-color-at-higher-risk-of-serious-illness-if-infected-with-coronavirus/
Description
Low-Income and Communities of Color at Higher Risk of Serious Illness if Infected with Coronavirus
URL
https://oklahoma.gov/covid19.html
Description
COVID-19: Oklahoma State Department of Health
URL
https://www.thecommunityguide.org/content/task-force-findings-increasing-vaccination
Description
CPSTF Findings for Increasing Vaccination

Learn more about this trial

CATCH-UP Vaccines: Extension of Community - Engaged Approaches to Testing in Community and Healthcare Settings for Underserved Populations (COVID-19)

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