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- Study Description
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Important Links and Information
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Request access via Authorized Access
- Instructions for requestors
- Data Use Certification (DUC) Agreement
- Talking Glossary of Genetic Terms
Adverse effects of the coronavirus disease 2019 (COVID19) pandemic on US society, health, and economy are widespread. The Collaborative Cohort of Cohorts for COVID-19 Research (C4R) aims to advance our knowledge on the impact of the COVID-19 pandemic in the United States. C4R is a diverse national prospective study comprising 14 long-standing prospective cohort studies and over 49,000 participants with extensive pre-COVID-19 phenotype data. C4R links pre-pandemic data on clinical and subclinical diseases and their risk factors, including behavior, cognition, biomarkers, and social determinants of health, to information on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and acute and post-acute COVID-related illness. Ascertainment of COVID-19 infection occurs via standardized questionnaires, adjudication of COVID-related hospitalizations and deaths, and SARS-CoV-2 serosurvey via dried blood spot cards. C4R is investigating the following research questions: 1) how pre-existing health conditions affect risk of severe or prolonged COVID-19 related illness; 2) how SARS-CoV-2 infection and COVID-19 illness affect long-term health; and 3) how the pandemic has affected health-related behaviors and non-COVID health outcomes. This resource will allow evaluation of risk and resilience factors for COVID-19 severity and long-term health effects.
The REasons for Geographic and Racial Differences in Stroke (REGARDS) cohort is one of the nation's largest, most comprehensive population-based cohorts, and it uses innovative home- and telephone-based data collection. REGARDS centrally recruited and initially examined 30,239 Black and White men and women aged ≥45 years in 2003-7 to understand why Southerners and Black Americans have a higher incidence of stroke and related diseases that affect brain health.
Data Being SubmittedWave 1 questionnaire data includes 397 variables for 8109 REGARDS participants in C4R.Wave 2 questionnaire data includes 448 variables for 6421 REGARDS participants in C4R.Dried Blood Spot/Serosurvey data includes 7 variables for 4058 REGARDS participants in C4R.Derived data includes 43 variables for 8606 REGARDS participants in C4R.Phenotype data includes 113 variables for 7880 REGARDS participants in C4R.
- Study Weblinks:
- Study Design:
- Prospective Longitudinal Cohort
- Study Type:
- Longitudinal Cohort
- Total number of consented subjects: 8707
- Subject Sample Telemetry Report (SSTR)
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Request access via Authorized Access
- Authorized Access
- Publicly Available Data
- Link to other NCBI resources related to this study
- Study Inclusion/Exclusion Criteria
REGARDS Inclusion Criteria:
- Aged 45 years or older
- African American or white
REGARDS Exclusion Criteria:
- Race other than African American or white
- Active treatment for cancer
- Medical conditions that would prevent long-term participation
- Cognitive impairment, judged by the telephone interviewer
- Residence in or inclusion on a waiting list for a nursing home
- Inability to communicate in English
REGARDS C4R Inclusion Criteria:
- REGARDS participants who:
- Are active
- Have completed the 2nd in-home exam
- Study History
The (REGARDS) cohort is one of the nation's largest, most comprehensive population-based cohorts, and it uses innovative home- and telephone-based data collection. REGARDS centrally recruited and initially examined 30,239 Black and White men and women aged ≥45 years in 2003-7 to understand why Southerners and Black Americans have a higher incidence of stroke and related diseases that affect brain health. REGARDS has conducted annual follow-up with participants since enrollment and pursues medical records for relevant events. In 2020, REGARDS worked with C4R to understand the impact of SARS-CoV2 on the cohort.
- Selected Publications
- Diseases/Traits Related to Study (MeSH terms)
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- Primary Phenotype: COVID-19
- SARS-CoV-2
- COVID-19 Serological Testing
- COVID-19 Testing
- COVID-19 Vaccines
- Authorized Data Access Requests
- Study Attribution
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Principal Investigator
- Elizabeth C. Oelsner, MD, MPH. Columbia University Irving Medical Center, New York, NY, USA.
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Co-Principal Investigator
- R. Graham Barr, MD, DrPH. Columbia University Irving Medical Center, New York, NY, USA.
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Co-Investigator
- Pallavi Balte, MBBS, MPH, PhD. Columbia University Irving Medical Center, New York, NY, USA.
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Cohort Principal Investigators
- Virginia Howard. University of Alabama, Birmingham, AL, USA.
- Suzanne Judd. University of Alabama, Birmingham, AL, USA.
- Mary Cushman. University of Vermont, Burlington, VT, USA.
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Cohort Co-Investigator
- Emily Levitan. University of Alabama, Birmingham, AL, USA.
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Data Manager
- Ya Yuan. University of Alabama, Birmingham, AL, USA.
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Principal Investigator