Atlas Logo
Danish High Risk and Resilience Study (VIA)
Danish High Risk and Resilience Study logo
BACK
Sample details

The VIA is a representative nationwide longitudinal multi-informant cohort study consisting of over 500 children born to parents with schizophrenia, bipolar disorder, or population-based controls. The participating families were recruited from Danish registers and investigated thoroughly when the children were 7 years old, referred to as the VIA 7 study. The second wave of assessments, the VIA 11 study, was carried out when the children were 11 years of age, and the third wave, the VIA 15 study, was carried out when the children were 15 years of age.

Study design
Cohort - birth

Number of participants at first data collection

522 (participants)

Age at first data collection

7 years (participants)

Participant year of birth

2004 - 2009 (participants)

Participant sex
All

Representative sample at baseline?
The Danish population born in 2004 - 2009.

Sample features

Adolescents
Children and young people
Patients and clinical populations
Dataset details

Country

Denmark

Year of first data collection

2013

Primary Institutions

Aarhus University Hospital (Aarhus Universitetshospital, AUH)

Copenhagen University Hospital (Rigshospitalet)

Gentofte Hospital (Gentofte Hospitalsvej)

University of Copenhagen (Københavns Universitet, KU)

Links

xn--viaundersgelsen-eub.org/

doi.org/10.1186/s12888-015-0616-5

Funders

Beatrice Surovell Haskell Fund for Child Mental Health Research of Copenhagen

Capital Region of Denmark (Region Hovedstaden)

Independent Research Fund Denmark (Danmarks Frie Forskningsfond)

Innovation Foundation

Lundbeck Foundation

Ongoing?
Yes

Data types collected

neuroImagingData
mentalHealthData
qualitativeData
dataLinkage
Quantitative data collection
  • Computer, paper or task testing (e.g. cognitive testing, theory of mind doll task, attention computer tasks)
  • Interview – face-to-face
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Wearable devices
Qualitative data collection
  • Ethnography or participant observation
Neuroimaging data collection
  • Electroencephalography (EEG)
  • Functional magnetic resonance imaging (fMRI)
  • Magnetic Resonance Imaging (MRI)
  • Magnetoencephalography (MEG)
Linked or secondary data
  • Education data
  • Healthcare data
  • Other government data
  • Tax, income & benefit data
Features

Engagement

  • Community engagement
  • Keywords

    Biological samples/biospecimens
    Clinical outcomes
    Environment
    Gene-environment interactions (GxE)
    Genetic predisposition
    Human development
    Neurocognition
    Neuroimaging
    Contact us

    |

    FAQS

    |

    Privacy

    |

    © 2024 Louise Arseneault

    Platform by Delosis