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Manicaland General Population Cohort
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Sample details

This research conducts a population-based cohort survey to study HIV transmission dynamics and their impacts across 12 sites in Manicaland province, Zimbabwe, representing diverse socio-economic strata. Between 1998 and 2013, six survey rounds gathered extensive data on HIV prevalence, incidence, and related mortality among children and adults. Each round included household censuses, interviews with participants (including HIV testing), verbal autopsy interviews with caregivers of past participants who have died since the previous round, and interviews with and collection of dried blood spot samples for HIV testing from women attending for antenatal check-ups at local health clinics. With phased enumeration to maintain data quality, the study provides insights into the epidemic over time.

Study design
Cohort, Cohort - open

Number of participants at first data collection

9,109 (participants)

Age at first data collection

15 - 54 years (participants)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Adults
Children and young people
Households and household members
People living with HIV
Population-based sample
Dataset details

Country

Zimbabwe

Year of first data collection

1998

Primary Institutions

Biomedical Research and Training Institute (BRTI)

Imperial College London (Imperial, ICL)

Links

manicalandhivproject.org/open-cohort.html

Funders

Bill & Melinda Gates Foundation

Wellcome Trust

Ongoing?
No

Data types collected

mentalHealthData
qualitativeData
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
  • Interview – phone
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Secondary data
  • Self-report questionnaire – online
  • Self-report questionnaire – paper or computer assisted
Qualitative data collection
  • Interviews or focus groups
Neuroimaging data collection
  • None
Linked or secondary data
  • Census data
Features

Engagement

  • Community engagement
  • Keywords

    Biological samples/biospecimens
    Fertility
    Human immunodeficiency virus (HIV)
    Migration
    Morbidity and mortality
    Sexual health and function
    Sociodemographics
    Treatment adherence
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