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Ontario Birth Study (OBS)
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Sample details

The OBS was launched in 2013 with pregnant women who were less than 17 weeks gestational age, recruited from antenatal clinics at Mount Sinai Hospital, Toronto, Canada. The collection of biological samples, clinical data, and questionnaire data has been incorporated into routine care, therefore the OBS is an open, longitudinal cohort with the intention to continue recruitment indefinitely. Phase 1 of recruitment was the initial 2-year pilot phase of the study that was launched in January 2013, and recruitment was completed in November 2015 (with births occurring up to May 2016). Within the baseline sample, 39% of mothers were 35 years of age or older, including 7% of women who were 40 years of age or older. Most of the parents identified as being White (of European descent; 69% of mothers and 72% of fathers), but there were other ethnicities represented, particularly Asian, consistent with the diverse Toronto population. There were 87% of women who reported that they were currently married, and most parents had completed university education (84% of mothers and 75% of fathers).

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

Number of participants at first data collection

1,272 (participants)

Recruitment is ongoing

Age at first data collection

≥ 18 years (participants)

Participant year of birth

Varied (participants)

Participant sex
Female

Representative sample at baseline?
No

Sample features

Mother and child dyad
Pregnant people
Dataset details

Country

Canada

Year of first data collection

2013

Primary Institutions

Lunenfeld-Tanenbaum Research Institute (LTRI)

Mount Sinai Hospital (MSH)

Links

ontariobirthstudy.com/

Profile paper DOI

doi.org/10.1111/ppe.12473

Funders

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

Lunenfeld-Tanenbaum Research Institute

Mount Sinai Hospital (MSH)

Ongoing?
Yes

Data types collected

mentalHealthData
dataLinkage
Quantitative data collection
  • 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
  • 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
    Gene-environment interactions (GxE)
    Maternal health
    Perinatal
    Pregnancy outcomes
    Pregnancy-birth cohort
    Prenatal exposures
    Routine care
    Social functioning
    Trajectory
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