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Young Lives Vietnam
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Sample details

The Young Lives Vietnam study, part of the wider Young Lives study, began in 2002 with around 3,000 children from Vietnam. Two cohorts of children (aged 6-18 months and 7-8 years) were recruited using a sentinel site surveillance system, selecting five regions based on regional and urban/rural differences, and four communes from each region using a pro-poor selection rule based on poverty rankings. Follow-ups occur every 3-4 years to track their development over a 15-year period.

Study design
Cohort - accelerated

Number of participants at first data collection

2,002 (younger cohort participants)

1,000 (older cohort participants)

Age at first data collection

6 - 18 months (younger cohort participants)

7 - 8 years (older cohort participants)

Participant year of birth

2001 - 2002 (younger cohort participants)

1994 - 1995 (older cohort participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Accelerated cohort
Children and young people
Dataset details

Country

Vietnam

Year of first data collection

2002

Primary Institutions

University of Oxford

Vietnam Academy of Social Sciences (Viện Hàn lâm Khoa học xã hội Việt Nam, VASS)

Links

younglives.org.uk/vietnam

academic.oup.com/ije/article/42/3/701/909722

Profile paper DOI

doi.org/10.1093/ije/dyab111

Funders

Bernard van Leer Foundation

Department for International Development (DFID) now known as Foreign, Commonwealth & Development Office (FCDO)

Echidna Giving

Economic and Social Research Council (ESRC)

Foreign, Commonwealth & Development Office (FCDO)

Ongoing?
Yes

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
  • Secondary data
  • Self-report questionnaire – paper or computer assisted
Qualitative data collection
  • Creative, arts-based and visual methods
  • Ethnography or participant observation
  • Interviews or focus groups
Neuroimaging data collection
  • None
Linked or secondary data
  • Geographic, spatial & environmental data
Features

Engagement

  • Patients, service users, lived experience involvement
  • Participant or community advisory groups
  • Community engagement
  • Keywords

    Cognition
    Diet and nutrition
    Education
    Ethnic minorities
    Growth
    Human development
    Life outcomes
    Low socioeconomic outcomes
    Physical health
    Poverty
    Rural areas

    Consortia and dataset groups

    Young Lives
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