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Clinical Trials/NCT05805163
NCT05805163
Not Yet Recruiting
N/A

A Culturally Relevant Communication and Support Plan to Ensure Access to and Use of Covid-19 Testing for Francophone African Born Immigrants

Texas Woman's University0 sites100 target enrollmentSeptember 2023
ConditionsCOVID19 Testing

Overview

Phase
N/A
Intervention
Not specified
Conditions
COVID19 Testing
Sponsor
Texas Woman's University
Enrollment
100
Primary Endpoint
Return rate
Status
Not Yet Recruiting
Last Updated
3 years ago

Overview

Brief Summary

The goal of this clinical trial is to test the effectiveness of a culturally sensitive COVID-19 testing intervention designed for Francophone (French speaking) African Born Immigrants (FABI) . The main question this study aims to answer is whether or not a a culturally sensitive COVID-19 educational pamphlet added to the home-based test will improve testing rates compared to receiving a standard home-based test alone.

Detailed Description

Upon consenting, all participants will receive basic COVID-19 testing instructions from trained bilingual/bicultural Francophone African Born Immigrant (FABI) Community Health Workers (CHW's). Next, participants will be randomly assigned to either the control or intervention study arms. In the control condition (n=50) participants will receive a standard COVID-19 home-based test kit. In contrast, those assigned to the intervention condition (n=50) will receive the same COVID-19 home-based test kit plus a FABI culturally sensitive COVID-19 educational pamphlet. Lastly, (n=10) participants from each arm will be randomly selected to participate in qualitative interviews to assess their experiences with CHWs and their test kit.

Registry
clinicaltrials.gov
Start Date
September 2023
End Date
May 2024
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • FABI living in Dallas Fort Worth (DFW) -

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Return rate

Time Frame: Tests returned within 3 months

Ratio of returned tests over total tests provided

Secondary Outcomes

  • Qualitative assessment(2 months)

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