Increasing COVID-19, Influenza, and Pneumonia Vaccine Uptake
Withdrawn before enrolling · Not applicable
Conditions studied: Covid19, Influenza, Pneumonia, Vaccine Refusal
In brief
This proposed study seeks to community knowledge and understand the experience of underserved communities in the exploration of reducing health disparities and increasing vaccine uptake and acceptability COVID-19, influenza, and pneumonia for AA and Latinx populations. Unique in its design, it has the following characteristics: 1) multifaceted, 2) culturally tailored, 3) community-based, and 4) mixed methods in which the outcomes of interest will be measured before and after the intervention with 18-month interval. Furthermore, we seek to enhance our partnerships and collaborations with churches in South Los Angeles by supporting efforts to encourage COVID-19, influenza, and pneumonia vaccination uptake among underserved minorities in one of the most challenged and hard-to-reach population areas in the nation.
Key facts
- Study ID
- NCT04761692
- Run by
- Charles Drew University of Medicine and Science
- People needed
- 0
- Starts
- 2022-10-01
- Expected to finish
- 2026-12-31
- Last updated by the study team
- 2022-08-19
Who can join
Age: 65 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Parishioner at a church receiving the VEPMP intervention
- Identify as African American or Latinx,
- at least 65 years and older
- Have Not received a vaccine for COVID-19, influenza, or pneumonia within the previous 24 months
- Agrees to study terms, which include follow-up interviews 9 and 18 months after study enrollment
You may not qualify if…
- Does not attend or identify as a Parishioner at a church receiving the VEPMP intervention
- Does not identify as African American or Latinx
- Under the age of 65 years
- Received all vaccine doses for COVID-19, influenza, or pneumonia within the previous 24 months
Where it is running
- Charles R. Drew University of Medicine & Science — Los Angeles, California, United States
Full record on ClinicalTrials.gov
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