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Centers for AIDS Research Network of Integrated Clinical Systems (CNICS)
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Sample details

The CNICS is a United States of America-based, clinic-integrated cohort study established to investigate long-term clinical outcomes among people living with human immunodeficiency virus (HIV) in the era of highly active antiretroviral therapy (HAART). As of 2024, it comprises over 49,000 HIV-infected adults receiving care at seven academic medical centres across the country. Participants were recruited from routine clinical care at CNICS-affiliated sites beginning in 1995, with ongoing enrollment of approximately 1,400 new patients annually to reflect the evolving HIV epidemic and treatment landscape. Recruitment has expanded over time to include additional Centers for AIDS Research Network (CFAR) sites such as Johns Hopkins University, enhancing geographic and ethnic representation. Participants are followed through routine clinical visits, typically every three months, with data captured prospectively via electronic medical records and supplemented by patient-reported outcomes collected approximately every six months.

Study design
Cohort, Cohort - clinical

Number of participants at first data collection

49,635 (patients as of 2024)

Recruitment is ongoing

Age at first data collection

≥ 18 years (patients)

Participant year of birth

Varied (patients)

Participant sex
All

Representative sample at baseline?
No

Sample features

Adults
People living with HIV
Dataset details

Country

United States of America

Year of first data collection

1995

Primary Institutions

University of Alabama at Birmingham (UAB)

Links

sites.uab.edu/cnics/

doi.org/10.2105/AJPH.2012.301162

Profile paper DOI

doi.org/10.1093/ije/dym231

Funders

National Cancer Institute (NCI)

National Heart, Lung, and Blood Institute (NHLBI)

National Institute of Allergy and Infectious Diseases (NIAID)

National Institute of Mental Health (NIMH)

National Institute on Drug Abuse (NIDA)

Ongoing?
Yes

Data types collected

mentalHealthData
dataLinkage
Quantitative data collection
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Secondary data
  • Self-report questionnaire – paper or computer assisted
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Healthcare data
  • Mortality data
Features

Engagement

  • None
  • Keywords

    Acquired immunodeficiency syndrome (AIDS)
    Antiretroviral therapy (ART)
    Biological samples/biospecimens
    Clinical outcomes
    Comorbidity
    Electronic health records
    Human immunodeficiency virus (HIV)
    Multi-site
    Substance use
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