NIEHS Clinical Research Unit (CRU)
Research Triangle Park, North Carolina, 27709, United States
Location status: Recruiting
NCT Number: NCT04983251
Background:
Inequalities in COVID-19 infection, hospitalization, and death in under-studied, under-represented, and under-reported groups of people are severe. A growing number of studies have assessed the impact of individual risk factors. But few studies have assessed which factors are the greatest drivers of COVID-19 disparities from a wider perspective.
Objective:
To understand the long-term impacts of COVID-19 on minority women and their families to assist in developing community-based programs to help in recovery.
Eligibility:
Healthy people aged 18 and older who reside in North Carolina.
Design:
Participants will take a 45-minute online survey. The survey will cover their demographics, community, health, lifestyle, household, and environment.
Participants may choose to have tests. They may visit the Clinical Research Unit. They may also have a home visit for these tests. In some cases, they may mail samples to the study team in prepaid envelopes.
Participants may take an optional 15 minute survey about their reproductive history.
Participants may give a blood sample.
Participants may give a urine sample. They will fill out a log and return with their sample.
Participants may give saliva samples.
Participants may give toenail samples from each toe.
Participants may give dust samples. They will be given 8 alcohol swabs. Two will be for testing. They will be asked to swipe a total of 3 door frames. Each door frame should be in a different room of the house.
Participants may be given silicone wristbands to wear for 1 week. This is to measure their exposure to air pollutants.
Participants may be contacted in the future for follow-up. They may be contacted by phone, email, or letter.
Interested in participating?
Request Info18 year–100 year
Female
Observational
Research Triangle Park, North Carolina, 27709, United States
Location status: Recruiting
Study Description:
This is a cross-sectional population-based survey designed within a syndemic framework to characterize the impacts of the COVID-19 pandemic on women in under-served, under-studied, under-represented, and under-reported (U4) populations. We hypothesize that U4 women are experiencing and will have experienced a worsening of mental, physical, and socio-economic status as a result of the COVID-19 pandemic and that pre-pandemic indicators of U4 status and related exposures will be associated with adverse mental, physical, and SES effects of the COVID-19 pandemic. The study ultimately seeks to collect baseline data for a long-term follow-up study of U4 women, as well as identify high impact targets for public health interventions to build resiliency in U4 communities.
Objectives:
Primary Objectives:
Secondary Objectives:
Tertiary/Exploratory Objectives:
(a) generalize pandemic impacts across multiple U4 populations using pooled meta-analysis; and (b) to understand how U4 status interacts with environmental, health, and social risk factors to produce disparities in pandemic-associated impacts by comparing U4 and non-U4 populations.
Endpoints:
Primary. Characterization of mental health, physical health and socioeconomic impacts during and following the pandemic.
Secondary. Primary endpoints plus direct and indirect experiences with SARS-CoV-2 infection.
Tertiary/Exploratory.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
In order to be eligible to participate in this study, an individual must meet all of the following criteria:
Exclusion criteria
An individual who meets any of the following criteria will be excluded from participation in this study:
-Any condition that, in the investigator's opinion, places the participant at undue risk for complications associated with required study procedures.
Time frame: 2 years
(1)Characterize the mental, physical, and socio-economic effects of the COVID-19 pandemic on women in under-studied, under-represented, and under-reported (U4) populations within a syndemic framework. (2) Determine whether there was a worsening of mental, physical, and socio-economic status before, during, and following the COVID-19 pandemic. (3) Characterize the biological, behavioral, environmental, sociocultural, and structural impacts of the COVID-19 pandemic on factors that affect reproductive risk factors among U4 women.
Time frame: 2 years
(1) Quantify cross-sectional associations between retrospective pre-pandemic indicators of U4 status and related exposures (i.e., urban vs. rural; pre-existing physical and mental health disparities; risk factors for maternal mortality; experiences of racism; social factors, and environmental, occupational, and housing exposures) with adverse mental, physical, and SES effects of the COVID-19 pandemic. (2) Characterize the direct and indirect experiences of U4 women with SARS-CoV-2 infection. (3) Identify opportunities for interventions to address maternal mortality in U4 women in the context of an ongoing global pandemic of COVID-19.
Contact information is provided by the study sponsor or research team.
Jaslyn A Grullon
CONTACT
Joan P Packenham, Ph.D.
CONTACT
National Institute of Environmental Health Sciences (NIEHS)
Nih
Women's Health Awareness Community Resiliency, Environmental Action and Collaborations for Health (REACH) Equity
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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