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Alberta Pregnancy Outcomes and Nutrition (APrON)
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Sample details

The APrON study follows a cohort of pregnant women, their partners, and their children in Alberta, Canada. Between May 2009 and June 2012, over 2,100 pregnant women and over 1,300 of their male partners were recruited from Alberta's largest metropolitan areas, Calgary and Edmonton, when pregnant women were less than 27 weeks gestational age. The initial cohort completed questionnaires and clinical assessments three times during pregnancy and at 3 months postpartum. Follow-up questionnaires were provided when children were 6 months and 1, 2, 3, 5, and 8 years of age, with a further 12-year follow-up beginning in 2022.

Study design
Cohort - birth, Cohort - primary caregiver and child

Number of participants at first data collection

2,189 (pregnant women)

1,325 (male participants)

Age at first data collection

16 - 44 years (pregnant women)

18 - 52 years (male participants)

Birth (children)

Participant year of birth

Varied (pregnant women)

Varied (male participants)

2009 - 2012 (children)

Participant sex
All

Representative sample at baseline?
No

Sample features

Families
Pregnant people
Dataset details

Country

Canada

Year of first data collection

2009

Primary Institutions

Alberta Children's Hospital Foundation (ACHF)

Alberta Health Services (AHS)

Alberta Innovates

University of Alberta

University of Calgary

Links

apronstudy.ca/

doi.org/10.1111/j.1740-8709.2012.00433.x

Funders

Alberta Children’s Hospital Foundation (ACHF)

Alberta Innovates

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

Kids Brain Health Network (KBHN)

Mental Health Commission of Canada (Commission de la santé mentale du Canada)

Ongoing?
Yes

Data types collected

mentalHealthData
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 – online
  • Self-report questionnaire – paper or computer assisted
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Healthcare data
  • Medical birth registry
Features

Engagement

  • Participant or community advisory groups
  • Community engagement
  • Keywords

    Biological samples/biospecimens
    Diet and nutrition
    Human development
    Infant biosamples
    Maternal mental health
    Maternal morbidity
    Pregnancy outcomes
    Sub-studies
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