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Early Quantitative Characterization of Reciprocal Social Behavior (ERSB)
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Sample details

The ERSB study was focused on the development, validation, and standardisation of quantitative methods to measure core components of variation in the social development of young children. Participants were parent-child dyads including toddler-aged twins born from 2011 to 2013, recruited from birth registries in Missouri and California, the United States of America. Around 300 participants in Missouri and 400 participants in California completed a baseline assessment beginning in 2013. Participants were assessed when children were 18, 24, 36, and 48 months of age.

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

Number of participants at first data collection

314 (parent-child dyads in Missouri)

402 (parent-child dyads in California)

Age at first data collection

18 months (children in Missouri)

Varied (parents in Missouri)

18 months (children in California)

Varied (parents in California)

Participant year of birth

2011 - 2013 (children in Missouri)

Varied (parents in Missouri)

2012 (children in California)

Varied (parents in California)

Participant sex
All

Representative sample at baseline?
No

Sample features

Caregiver and child dyad
Children and young people
Dizygotic and monozygotic twins
Hispanic/Latino populations
Parents
Dataset details

Country

United States of America

Year of first data collection

2013

Primary Institutions

Washington University in St. Louis (WashU)

Links

reporter.nih.gov/project-details/9058569

nda.nih.gov/edit_collection.html

doi.org/10.1111/jcpp.12391

doi.org/10.1186/s13229-024-00607-3

Funders

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

National Institutes of Health (NIH)

Ongoing?
No

Data types collected

mentalHealthData
Quantitative data collection
  • Computer, paper or task testing (e.g. cognitive testing, theory of mind doll task, attention computer tasks)
  • Interview – phone
  • Self-report questionnaire – paper or computer assisted
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • None
Features

Engagement

  • None
  • Keywords

    Autism and Autism-like conditions
    Behaviour
    Genetics
    Human development
    Psychosocial development
    Social behaviour
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