- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04867174
COVID-19 Vaccination Take-Up
March 1, 2024 updated by: National Bureau of Economic Research, Inc.
COVID-19 Vaccination Take-Up in a County-Run Medicaid Managed Care Population
In this work, the investigators are partnering with Contra Costa Health Services (CCHS), the department of health in Contra Costa County, CA, to measure COVID-19 vaccinations and other COVID-19 related preventive health behaviors in the county's Medicaid managed care population.
This work will test ways to increase COVID-19 vaccine uptake.
The investigators hypothesize that small financial incentives and other low-cost behavioral nudges can be used to increase vaccine uptake and reduce disparities in uptake among diverse racial/ethnic minority populations.
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
2701
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 Locations
-
-
California
-
Martinez, California, United States, 94553
- Contra Costa Health Plan
-
-
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
No
Description
Inclusion Criteria:
- age 18 and over
- member of Contra Costa Health Plan (CCHP)
Exclusion Criteria:
- contraindications to vaccination, as determined by county health plan or other medical staff.
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: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Placebo Comparator: Control Arm
No messaging about COVID-19 vaccination
|
Each of the study arms, including the no message/control arm, will be interacted with different financial incentives (N=5,000)
In addition, study arms will be randomly assigned a convenient link to the county public vaccine appointment scheduling system highlighted for participants (N=5,000).
|
|
Experimental: Emotional message
Participants view an emotional video from the state of California about getting back to normal.
|
Each of the study arms, including the no message/control arm, will be interacted with different financial incentives (N=5,000)
In addition, study arms will be randomly assigned a convenient link to the county public vaccine appointment scheduling system highlighted for participants (N=5,000).
|
|
Experimental: Safety and effectiveness message
Participants view a video with information about the safety and effectiveness of the COVID-19 vaccines
|
Each of the study arms, including the no message/control arm, will be interacted with different financial incentives (N=5,000)
In addition, study arms will be randomly assigned a convenient link to the county public vaccine appointment scheduling system highlighted for participants (N=5,000).
Randomized to a messenger who is race concordant with the participant
Randomized to a messenger who is gender concordant with the participant
|
|
Experimental: Consequences message
Participants view a video with information about the consequences of not getting vaccinated against COVID-19.
|
Each of the study arms, including the no message/control arm, will be interacted with different financial incentives (N=5,000)
In addition, study arms will be randomly assigned a convenient link to the county public vaccine appointment scheduling system highlighted for participants (N=5,000).
Randomized to a messenger who is race concordant with the participant
Randomized to a messenger who is gender concordant with the participant
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Rate of COVID-19 Vaccination at 1 Month
Time Frame: 1 month
|
Percent of the population with at least one COVID-19 vaccination
|
1 month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Rate of COVID-19 vaccination at 6 months
Time Frame: 6 months
|
Percent of the population with at least one COVID-19 vaccination
|
6 months
|
|
COVID-19 vaccination
Time Frame: 1 year
|
COVID-19 vaccination at 1-year
|
1 year
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Vaccine Intentions
Time Frame: 30 days
|
Stated intention of receiving COVID-19 vaccination in the next 30 days (0% - 100% probability)
|
30 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
May 24, 2021
Primary Completion (Actual)
August 15, 2021
Study Completion (Actual)
May 24, 2022
Study Registration Dates
First Submitted
April 27, 2021
First Submitted That Met QC Criteria
April 28, 2021
First Posted (Actual)
April 30, 2021
Study Record Updates
Last Update Posted (Actual)
March 28, 2024
Last Update Submitted That Met QC Criteria
March 1, 2024
Last Verified
March 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 27165
- P30AG034532 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Our partner will not allow data sharing.
Code will be shared.
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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