Atlas Logo
Themba Lethu Clinical Cohort
BACK
Sample details

The Themba Lethu Clinical Cohort follows patients enrolled in the HIV Care and Treatment program at the Themba Lethu Clinic (TLC) in Johannesburg, Gauteng Province, South Africa. The cohort consists of all patients who have tested positive for the human immunodeficiency virus (HIV) and have ever enrolled for HIV care at the TLC since the national rollout of the anti-retroviral therapy (ART) program in April 2004. As of 2011, the cohort consists of over 8,000 participants in pre-ART care and over 21,000 receiving ART, resulting in a total cohort of over 29,000 patients. As of 2016, the Themba Lethu Clinical Cohort has been incorporated into the Right to Care Clinical HIV Cohort, which includes nine other study sites. Participants are generally followed up every 3 to 6 months.

Study design
Cohort - clinical

Number of participants at first data collection

29,318 (participants as of 2011)

Recruitment is ongoing

Age at first data collection

≥ 18 years (participants)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Adults
People living with HIV
Dataset details

Country

South Africa

Year of first data collection

2004

Primary Institutions

Boston University (BU)

Duke University

Themba Lethu Clinic, Helen Joseph Hospital

University of the Witwatersrand, Johannesburg

Links

wits.ac.za/clinicalmed/research-units/clinical-hiv-research-unit/

righttocare.org/projects/the-themba-lethu-clinic-programme/

Profile paper DOI

doi.org/10.1093/ije/dys029

Funders

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

National Institute of Allergy and Infectious Diseases (NIAID)

President's Emergency Plan for AIDS Relief (PEPFAR)

Right to Care (RTC)

United States Agency for International Development (USAID)

Ongoing?
Yes

Data types collected

dataLinkage
Quantitative data collection
  • Interview – face-to-face
  • 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
    Healthcare access and use
    Human immunodeficiency virus (HIV)
    Medication
    Contact us

    |

    FAQS

    |

    Privacy

    |

    © 2024 Louise Arseneault

    Platform by Delosis