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Quebec Newborn Twin Study (QNTS)
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Sample details

QNTS follows a birth cohort of over 1,300 twins born between April 1995 and December 1998 in the Greater Montreal area, Québec, Canada. Twin births within this time period were identified using the Québec Newborn Twin Registry, with mothers subsequently contacted through information held by the Québec Bureau of Statistics. Twins have been assessed at 16 time points across childhood and adolescence, with the latest data collection occurring at age 19. Multiple informants have provided information throughout the study, including the twins, parents, and teachers.

Study design
Cohort - birth, Cohort - twin

Number of participants at first data collection

1,324 (twins)

662 (families)

Age at first data collection

6 months (twins)

Varied (families)

Participant year of birth

1995 - 1998 (twins)

Varied (families)

Participant sex
All

Representative sample at baseline?
No

Sample features

Dizygotic and monozygotic twins
Family members
Newborns, infants and babies
Dataset details

Country

Canada

Year of first data collection

1995

Primary Institutions

Laval University (Université Laval)

Links

research.chusj.org/en/Axes-de-recherche/Les-unites-de-recherche-clinique/Unites-de-recherche-clinique/Unite-de-recherche-clinique-en-inadaptation-psycho/Etude-des-jumeaux-nouveau-nes-du-Quebec-(EJNQ)

maelstrom-research.org/study/ejnq

research.chusj.org/en/Axes-de-recherche/Les-unites-de-recherche-clinique/Unites-de-recherche-clinique/Unite-de-recherche-clinique-en-inadaptation-psycho/Etude-des-jumeaux-nouveau-nes-du-Quebec-(EJNQ)

Profile paper DOI

doi.org/10.1017/thg.2019.74

Funders

Social Sciences and Humanities Research Council (SSHRC)

Canadian Institutes of Health Research (CIHR, Instituts de recherche en santé du Canada, IRSC)

National Health Research Development Program (NHRDP)

Quebec Fund for Research on Society and Culture (Fonds Québécois de la Recherche sur la Société et la Culture, FQRSC)

Research Fund in Quebec Health (Fonds de la Recherche en Santé du Québec, FRSQ)

Ongoing?
Yes

Data types collected

neuroImagingData
mentalHealthData
qualitativeData
dataLinkage
Quantitative data collection
  • Activity log (e.g. food, sleep, exercise)
  • Computer, paper or task testing (e.g. cognitive testing, theory of mind doll task, attention computer tasks)
  • Interview – face-to-face
  • Interview – online
  • 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
  • Ethnography or participant observation
Neuroimaging data collection
  • Electroencephalography (EEG)
Linked or secondary data
  • Healthcare data
  • Medical birth registry
Features

Engagement

  • Community engagement
  • Keywords

    Behavioural problems
    Biological samples/biospecimens
    Cognitive assessments
    Infant biosamples
    Multiple informants
    Observational study
    School environment
    Sub-studies

    Consortia and dataset groups

    COllaborative project of Development of Anthropometrical measures in Twins (CODATwins) project
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