Actively Recruiting
Improving the Collaborative Health of Minority COVID-19 Survivor and Carepartner Dyads
Led by University of South Carolina · Updated on 2025-05-16
500
Participants Needed
1
Research Sites
182 weeks
Total Duration
On this page
Sponsors
U
University of South Carolina
Lead Sponsor
N
National Institute of Nursing Research (NINR)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study tests the efficacy of a dyadic intervention to mitigate the adverse health consequences of severe acute respiratory syndrome coronavirus 2 (SARS- CoV-2 )(COVID-19) in African American (AA) adults with pre-existing chronic health conditions and their informal carepartners (IC). Socioeconomically disadvantaged, older, and Black/African American from rural regions are burdened with greater rates of chronic diseases such as diabetes, hypertension, chronic kidney disease, cardiovascular disease, and stroke.
CONDITIONS
Official Title
Improving the Collaborative Health of Minority COVID-19 Survivor and Carepartner Dyads
Who Can Participate
Eligibility Criteria
You may qualify if you...
- African American adults aged 18 years and older who survived COVID-19
- Male or female participants living in medically underserved or rural areas of South Carolina
- History of COVID-19-related hospitalization, emergency room, or urgent care visit since March 11, 2020
- Previous diagnosis of type 2 diabetes, hypertension, cardiovascular disease, chronic kidney disease, or stroke for more than 3 months
- Carepartners aged 18 years and older, male or female
- Carepartners living on the same property or within 40 miles of the survivor
- Carepartners primarily responsible for unpaid care or social support at home
You will not qualify if you...
- Survivors or carepartners currently enrolled in related clinical trials
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of South Carolina
Columbia, South Carolina, United States, 29208
Actively Recruiting
Research Team
S
Study PI
CONTACT
P
Program Coordinator
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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