A Study to Assess Infection Rate of Severe Acute Respiratory Syndrome - CoronaVirus 2 (SARS-CoV-2) and It's Affect on Quality of Life in Adult Volunteers in Lake County, Illinois

Completed

Conditions studied: Severe Acute Respiratory Syndrome - CoronaVirus 2 (SARS-CoV-2)

In brief

Coronavirus disease 2019 (COVID-19) is an infectious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Lung failure is the main cause of death related to COVID-19 infection. The main objective of this study is to assess infection of SARS-CoV-2 and how quality of life is affected in adult volunteers in Lake County, Illinois. Volunteers will be recruited through digital advertisements and participants will be required to fill an online questionnaire. Upon consent, participants will be required to provide nasal swab and blood sample. Approximately 1250 adult volunteers living or working in Lake County, IL will be enrolled. Participants will be followed for approximately 9 months and will be required to provide nasal swab and blood samples every 3 months and complete questionnaires every 2 weeks. There may be higher treatment burden for participants in this trial. Participants will be monitored by medical assessments, blood tests and questionnaires.

Key facts

Study ID

NCT04611230

Run by

AbbVie

People needed

1007

Starts

2020-11-05

Expected to finish

2021-10-27

Last updated by the study team

2022-10-10

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Currently living or employed in Lake County, Illinois.
• Have regular access to computer, smartphone or tablet and sufficient internet access to connect to study platform.
• Willing and able to provide informed consent for collection of online data and of respiratory and blood specimens.
• Willing and able to follow the procedures of the study.
• Able to complete survey in English or Spanish.

You may not qualify if…

• Unable to provide informed consent.
• Unable to perform the requested study tasks and unable or unwilling to assign a proxy informant to complete the tasks.
• Hospitalized at the time of study enrollment.

Where it is running

• Great Lakes Clinical Trials /ID# 224874 — Chicago, Illinois, United States

Full record on ClinicalTrials.gov

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