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HAART Observational Medical Evaluation and Research Cohort (HOMER)
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Sample details

The HAART HOMER cohort was established in 1996 to maintain a prospective record of clinical measurements and medication profiles of a subset of Drug Treatment Program (DTP) participants initiating Highly Active Antiretroviral Therapy (HAART) in British Columbia (BC), Canada. This unique cohort provides a comprehensive data source to investigate mortality, prognostic factors, and treatment response among people living with human immunodeficiency virus (HIV) in BC from the inception of HAART. The cohort is updated annually. The 5,229 individuals enrolled in the HOMER cohort as of 2012 represented approximately 63% of the 8,327 patients who had ever accessed ART through the DTP up until 30 June 2011.

Study design
Cohort - clinical

Number of participants at first data collection

5,229 (participants as of 2012)

Recruitment is ongoing

Age at first data collection

≥ 19 years (participants)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Patients and clinical populations
People living with HIV
Dataset details

Country

Canada

Year of first data collection

1996

Primary Institutions

University of British Columbia (UBC)

Links
No website available

Profile paper DOI

doi.org/10.1093/ije/dyu046

Funders

British Columbia PharmaCare

Ongoing?
Yes

Data types collected

dataLinkage
Quantitative data collection
  • Secondary data
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Census data
  • Healthcare data
Features

Engagement

  • None
  • Keywords

    Acquired immunodeficiency syndrome (AIDS)
    Human immunodeficiency virus (HIV)
    Infectious disease
    Morbidity and mortality
    Pharmacological treatment
    Treatment experiences and outcomes

    Consortia and dataset groups

    Antiretroviral Therapy Cohort Collaboration (ART-CC)
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