COVID-19, Health Care Worker (HCW)
Conditions
Brief summary
The HERO Registry provides a resource for collecting information on Healthcare Workers (HCWs) currently working in the United States, and their families and communities. The overall goal of the Registry is to develop the infrastructure necessary to create and engage a community of people who may be eligible for participation in future research studies, including those of COVID-19 prophylaxis and treatment.
Detailed description
The HERO Registry provides a resource for collecting information on Healthcare Workers (HCWs) currently working in the United States, and their family members and communities. The overall goal of the Registry is to create and engage a community of HCWs and their families and communities who may be eligible for participation in future research studies, including those of COVID-19 prophylaxis and treatment. The HERO registry will create a repository of adults interested in COVID-19 research that can be eligible for future research studies. The main objectives of the study are 1) create a virtual community of adult HCWs in the United States, and their families and communities, 2) Identify adults interested in engaging in upcoming research studies, including those related to COVID-19, and 3) Create a dataset of health related measurements, risk factors, and outcomes for future analysis. The population of interest is adult healthcare workers in the United States, and their families and communities. All analysis of the HERO Registry will be exploratory in nature. Analysis may include descriptive statistics of the cohort, statistical associations between variables of interest, and predictive modeling for health outcomes and behaviors. Analyses may be conducted on all participants in the HERO Registry or may be conducted on subpopulations defined based on clinical, demographic or other factors. There is no direct benefit to the participants for their participation in this study, but the information obtained will be used in scientific research and may be helpful to the participant or others in the future. Participants may experience indirect benefits such as learning about their own health, access to health data, and opportunities to participate in future research.
Interventions
None listed
Sponsors
Patient-Centered Outcomes Research Institute
Duke University
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 110 Years
Inclusion criteria
* A member of one of the following three groups: * Individual currently works in a setting where individuals receive healthcare (healthcare worker) (including emergency medical services), OR * A family member of a healthcare worker, OR * A member of a healthcare worker's community * Age ≥ 18 * Able to speak and read English or Spanish
Exclusion criteria
\* There are no specific
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Number and percent of participants who enroll in the HERO Registry Study by geographic region, age, COVID-19 risk factors, and past COVID-19 diagnosis | Up to 79 years |
| Distribution of COVID-19 risk factors by participant characteristics | Up to 79 years |
| Proportion of participants undergoing changes in health status (e.g. new diagnosis of COVID-19, ER visits, hospitalization) | Up to 79 years |
| Proportion of all participants enrolled in the HERO Registry who participate in an ancillary research study | Up to 79 years |
| Proportion of participants who continue to supply information about their health to the HERO Registry at various time points after their enrollment | Up to 79 years |
Countries
United States
Outcome results
None listed