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Healthy Brain Network (HBN)
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Sample details

The HBN is an ongoing initiative focused on creating and sharing a biobank of data from 10,000 New York area participants aged 5–21. The HBN Biobank houses multidisciplinary phenotypic data and multimodal brain imaging data. Recruitment for the study is ongoing since 2017, through advertisements that seek the participation of families who have concerns about one or more psychiatric symptoms in their child. Primary causes for exclusion of participation centre on the presence of acute safety concerns, cognitive or behavioural impairments that could interfere with participation or medical concerns that are expected to interfere with brain-related findings.

Study design
Cohort - research programme, Biobank

Number of participants at first data collection

4,136 (participants, as of 2024)

664 (participants)

Recruitment is ongoing

Age at first data collection

5 - 21 years (participants)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Adolescents
Children and young people
Dataset details

Country

United States of America

Year of first data collection

2017

Primary Institutions

Child Mind Institute

Links

fcon_1000.projects.nitrc.org/indi/cmi_healthy_brain_network/index.html

childmind.org/science/programs/healthy-brain-network/

healthybrainnetwork.org/

Funders

Brooklyn Nets

Charles and Helen Schwab Foundation

Gray Foundation

Howard & Irene Levine Family Foundation

Individual private funders

Ongoing?
Yes

Data types collected

neuroImagingData
mentalHealthData
Quantitative data collection
  • Audio or visual recordings (e.g. of child behaviour, facial expressions)
  • Computer, paper or task testing (e.g. cognitive testing, theory of mind doll task, attention computer tasks)
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Self-report questionnaire – paper or computer assisted
  • Voice capture (e.g. timbre, emotional fluctuations)
  • Wearable devices
Qualitative data collection
  • None
Neuroimaging data collection
  • Electroencephalography (EEG)
  • Functional magnetic resonance imaging (fMRI)
  • Magnetic Resonance Imaging (MRI)
Linked or secondary data
  • None
Features

Engagement

  • Community engagement
  • Patients, service users, lived experience involvement
  • Keywords

    Biological determinants
    Biological samples/biospecimens
    Clinical assessments
    Diagnostic markers
    Genetics
    Mental health
    Neuroimaging
    Psychiatry
    Research networks
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