Atlas Logo
Ontario HIV Treatment Network Cohort Study (OHTN)
Ontario HIV Treatment Network Cohort Study logo
BACK
Sample details

The OHTN is an open cohort comprised of individuals who have provided documentation of a positive human immunodeficiency virus (HIV)-antibody test or other laboratory evidence of HIV infection, and are patients at a participating clinic throughout Ontario, Canada. The study was initiated in 1994 as the HIV Ontario Observational Database and recruited its first participant in 1995. In that first phase, over 3,000 participants were enrolled and, as of December 2006, 1,656 were still active participants. As of May 2024, the study reports over 8,000 participants enrolled that are living with HIV. On average, participants were 41 years old at enrolment. The majority (60.3%) were MSM (men who have sex with men), although a sizeable minority (14.6%) were female and/or were infected through other modes of transmission. A large proportion (42%) were diagnosed in the 1990s and most enrolled several years after diagnosis. Participants are followed up by attending participating clinics.

Study design
Cohort - open, Cohort - clinical

Number of participants at first data collection

3,206 (participants)

Recruitment is ongoing

Age at first data collection

≥ 16 years (participants)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
The population receiving HIV care in Ontario, Canada.

Sample features

Patients and clinical populations
People living with HIV
Dataset details

Country

Canada

Year of first data collection

1995

Primary Institutions

University of Toronto

Links

ohtncohortstudy.ca/

ohtn.on.ca/

Profile paper DOI

doi.org/10.1093/ije/dyr230

Funders

HIV/AIDS Bureau

Ontario Ministry of Health and Long-Term Care

Ongoing?
Yes

Data types collected

mentalHealthData
dataLinkage
Quantitative data collection
  • Computer, paper or task testing (e.g. cognitive testing, theory of mind doll task, attention computer tasks)
  • Interview – face-to-face
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Secondary data
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Healthcare data
Features

Engagement

  • Participant or community advisory groups
  • Community engagement
  • Keywords

    Biological samples/biospecimens
    Clinical assessments
    Clinical cohort
    Disease prevention
    Healthcare access and use
    Human immunodeficiency virus (HIV)
    Infectious disease
    Interventions
    LGBTQIA+
    Retrospective
    Contact us

    |

    FAQS

    |

    Privacy

    |

    © 2024 Louise Arseneault

    Platform by Delosis