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 (CONTACT)

AbbVie

Status: Completed

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

Study type: Observational

Funder types: Industry

Identifiers

NCT04611230

H20-308

Details and patient eligibility

About

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.

Enrollment: 1,007 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 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.

Exclusion criteria

• 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.

Trial design

1,007 participants in 4 patient groups

Adult Volunteers (Low Risk Group)

Description:

Volunteers with jobs that do not require close contact with (i.e., within 6 feet of) the general public or co-workers.

Adult Volunteers (Medium - Low Risk Group)

Description:

Volunteers with jobs that require in-frequent contact with (i.e., within 6 feet of) the general public or co-workers.

Adult Volunteers (Medium - High Risk Group)

Description:

Volunteers with jobs that require frequent contact with (i.e., within 6 feet of) the general public or co-workers.

Adult Volunteers (High Risk Group)

Description:

Volunteers with jobs that require frequent and/or close contact with (i.e., within 6 feet of) individuals with high potential for exposure to known or suspected sources of COVID-19.