Examining How a Facilitated Self-Sampling Intervention and Testing Navigation Intervention Influences COVID-19 Testing
COVID-19
About this trial
This is an interventional other trial for COVID-19 focused on measuring COVID-19, antigen testing, decision making, testing behaviors, vulnerable populations, social networks
Eligibility Criteria
Inclusion Criteria: Aged 18 years or older Exclusion Criteria: Having been diagnosed with COVID-19 in the past 30 days based on a positive test (antigen or PCR) or a clinical diagnosis Having tested for COVID-19 with PCR or antigen test within the past 30 days
Sites / Locations
- The University of Texas Health Science Center, Brownsville
- The University of Texas Health Science Center, Houston
- University of Texas Health Science Center,Tyler
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Active Comparator
Facilitated Self-Sampling Intervention (FSSI)
Testing Navigation Intervention (TNI).
Control
Participants in the FSSI arm will receive education on COVID-19 testing and be provided with rapid antigen tests. Participants will also receive pre and post surveys.
Participants in the TNI arm will receive COVID-19 testing education and be navigated to PCR testing sites. Participants will also receive pre and post surveys.
Participants in the Control Group arm will receive a CDC-designed COVID-19 testing brochures, and pre and post surveys only.