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Cancer Vaccine
Increasing Willingness and Uptake of COVID-19 Vaccination for Coronavirus
N/A
Waitlist Available
Led By Sharon Cobb
Research Sponsored by Charles Drew University of Medicine and Science
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up intervention: 4 months; follow-up point: 3 months post-intervention
Awards & highlights
Study Summary
This trial will test a culturally tailored intervention to increase COVID-19 vaccination rates among African American and Latinx public housing residents in South Los Angeles.
Who is the study for?
This trial is for African American and Latinx adults over 18 living in specific South Los Angeles public housing who are hesitant about COVID-19 vaccines. Participants must speak English or Spanish but haven't received all recommended COVID-19 vaccines.Check my eligibility
What is being tested?
The study tests a culturally tailored educational program designed to increase the willingness and actual uptake of COVID-19 vaccinations among vaccine-hesitant residents in underresourced areas.See study design
What are the potential side effects?
Since this trial focuses on education and engagement rather than a medical intervention, it does not involve direct side effects from treatments. However, general side effects of the COVID-19 vaccines can include sore arm, fever, fatigue, headache, muscle pain.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ intervention: 4 months; follow-up point: 3 months post-intervention
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~intervention: 4 months; follow-up point: 3 months post-intervention
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Prevalence of vaccination uptake for COVID-19, influenza, and pneumonia using Vaccination History Self Report
Secondary outcome measures
Percentage of Participants Achieving Decreased Vaccine Hesitancy Levels of COVID-19 vaccine Using the NIH Toolbox Surveys on COVID-19
Percentage of Participants Achieving Increased Level of Behavior Change toward COVID-19 Vaccination Using the NIH Toolbox Surveys on COVID-19
Trial Design
1Treatment groups
Experimental Treatment
Group I: Increasing Uptake of COVID-19 VaccinationExperimental Treatment1 Intervention
This is a pre-experimental "one group pretest-posttest" design to increase COVID-19 vaccine uptake and completion among African American and Latinx public housing residents in South Los Angeles. The proposed intervention will employ (1) culturally sensitive, (2) theoretically based intervention that will be jointly delivered by our ACTIVATE triad leaders and our researchers. We will use the Information, Motivation, and Behavioral Skills (IMB) model and the Transtheoretical Model to implement the intervention.
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Who is running the clinical trial?
Charles Drew University of Medicine and ScienceLead Sponsor
51 Previous Clinical Trials
5,887 Total Patients Enrolled
1 Trials studying Vaccine Refusal
Sharon CobbPrincipal InvestigatorCharles R. Drew University of Medicine & Science
1 Previous Clinical Trials
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You must be able to speak either English or Spanish.You do not speak English or Spanish.I am hesitant about getting vaccines.I am willing to receive vaccines.You do not identify yourself as an African American or Latinx individual.You self-identify as a person of Latinx or African American ethnicity.
Research Study Groups:
This trial has the following groups:- Group 1: Increasing Uptake of COVID-19 Vaccination
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.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are there any current opportunities to participate in this research experiment?
"Clinicaltrials.gov attests that this clinical trial is actively seeking volunteers, which was initially posted on September 11th 2021 and updated as recently as January 26th 2022."
Answered by AI
How many individuals are enrolled in this experiment?
"Affirmative. According to information on clinicaltrials.gov, this medical trial is currently in search of patients. It was initially published on September 11th 2021 and has been updated most recently as of January 26th 2022. The study requires 600 participants from 1 research centre for completion."
Answered by AI
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