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The Impact of Community and Patient Engagement Practices on Vaccine Confidence in the United States
Sponsor: Tufts University
Summary
The primary objective of this study is to demonstrate an empirical relationship between community- engagement practices, and between patient-centric clinical trial design, execution and communication practices, and vaccine adoption experience. Our hypothesis is that patient-centric clinical trial activity, and community engagement in late-stage clinical trials and early-stage commercialization, reduces vaccine hesitancy and increases vaccine confidence among health care providers overall and within diverse patient communities and ultimately drives faster vaccine adoption.
Official title: Assessing the Relationship Between Patient Centric Clinical Trial Practices, Pre- and Post-Approval Community Engagement Practices, and Vaccine Hesitancy and Adoption
Key Details
Gender
All
Age Range
Any - Any
Study Type
OBSERVATIONAL
Enrollment
30
Start Date
2024-06
Completion Date
2025-02
Last Updated
2024-04-18
Healthy Volunteers
Not specified
Conditions
Interventions
Community Engagement Practice
Community engagement includes pre- and post-approval clinical trials that partnered and engaged with diverse public and patient communities; trusted community leaders; local advocacy groups; faith-based and civic organizations; community influencers; community health and government health communities.
Patient-Centric Protocol Element
Patient-centric clinical trial designs include those that solicited patient, investigative site and community input into protocol design and clinical trial feasibility; offered solutions that improved patient participation convenience and access; and that more fully and effectively communicated clinical trial knowledge to diverse public and patient communities, health care providers and community influencers.