CATCH-UP Vaccines: Extension of Community - Engaged Approaches to Testing in Community and Healthcare Settings for Underserved Populations (COVID-19)
COVID-19, Vaccine Refusal
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
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).
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
No Intervention
Experimental
Experimental
Experimental
Experimental
Experimental
Experimental
Experimental
Condition 1
Condition 2
Condition 3
Condition 4
Condition 5
Condition 6
Condition 7
Condition 8
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.