Atlas Logo
Nord-Trøndelag Health Study Young-HUNT Study (Young-HUNT)
BACK
Sample details

The Young-HUNT Study is the adolescent part of the Trøndelag Health Study (The HUNT Study), a population-based health study inviting all inhabitants, aged 13 years and above, of primarily the northern part of Trøndelag County (former Nord-Trøndelag) in the central part of Norway. The HUNT study has collected data in four subsequent surveys every 11th year from 1984 to 2017, but collections of adolescent data, aged 13 to 19 years, started for the first time in 1995. Young-HUNT1 to Young-HUNT2 cohort, a 4-year follow-up, included 2,399 participants followed from early adolescence (mean age was 13.9 years) to late adolescence. The Young-HUNT1 to HUNT3 cohort was an 11-year follow-up from adolescence (mean age was 15.9 years) to young adulthood. The Young-HUNT allows longitudinal follow-up into adulthood, as well as linkage to a wide range of regional and national health registries by means of the unique identification number allocated to all Norwegian residents.

Study design
Cohort

Number of participants at first data collection

2,399 (participants)

Age at first data collection

13 - 19 years (participants)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Young adults
Dataset details

Country

Norway

Year of first data collection

1995

Primary Institutions

Central Norway Regional Health Authority (Helse Midt-Norge RHF)

Norwegian Institute of Public Health (Folkehelseinstituttet, FHI, NIPH)

Norwegian University of Science and Technology (Norges teknisk-naturvitenskapelige universitet, NTNU)

Trøndelag County Municipality (Trøndelag fylkeskommune)

Links

ntnu.edu/hunt/young-hunt

doi.org/10.1093/ije/dys232

Profile paper DOI

doi.org/10.1093/ije/dyae013

Funders

AstraZeneca

Nord-Trøndelag County Municipality (Nord-Trøndelag fylkeskommune)

Norwegian Ministry of Health

Norwegian Women's Public Health Association (Norske Kvinners Sanitetsforening, NKS)

Research Council of Norway (Norges forskningsråd)

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 – paper or computer assisted
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Education data
  • Healthcare data
  • Medical birth registry
  • Mortality data
  • Social care data
  • Tax, income & benefit data
Features

Engagement

  • Community engagement
  • Keywords

    Cardiovascular health and disease
    Clinical assessments
    Health behaviour
    Human development
    Public health
    Quality of life
    School-based
    Tuberculosis

    Consortia and dataset groups

    Cross-cohort Harmonization Project for Tomorrow (CHPT)
    Contact us

    |

    FAQS

    |

    Privacy

    |

    © 2024 Louise Arseneault

    Platform by Delosis