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Danish National Health Survey (DNHS)
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Sample details

The DNHS aims to monitor the health and well-being of the Danish population. Formerly known as the DHMS, the study began in 1987 with 8,363 participants at baseline. Participants were followed up in 1994, 2000, and 2005, ending with 21,832 participants. These participants were then followed up through the Danish National Cohort Study (DANCOS), a registry-based follow-up database, to calculate the impact of risk factors on mortality through linkage. The study, now known as the DNHS, followed up participants from the DHMS alongside new participants, with 177,639 participants in total in 2010. Participants are from six mutually exclusive random subsamples: one from each of the five Danish regions and one national sample. They have been followed up in 2013, 2017, 2021, and 2023, with 183,372 participants as of 2017.

Study design
Cohort - open, Registry

Number of participants at first data collection

8,363 (participants)

Recruitment is ongoing

Age at first data collection

≥ 16 years (participants)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
The population of Denmark.

Sample features

Adults
Population-based sample
Dataset details

Country

Denmark

Year of first data collection

1987 (DHMS)

2010 (DNHS)

Primary Institutions

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

University of Southern Denmark (Syddansk Universitet, SDU)

Links

danskernessundhed.dk/Vejledning.html

doi.org/10.1177/1403494809341095

Funders

Capital Region of Denmark (Region Hovedstaden)

Central Denmark Region (Region Midtjylland)

Danish Ministry of Health

Danish Ministry of Interior and Health

National Board of Health

Ongoing?
Yes

Data types collected

mentalHealthData
dataLinkage
Quantitative data collection
  • Activity log (e.g. food, sleep, exercise)
  • Interview – face-to-face
  • 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
  • Education data
  • Employer data
  • Geographic, spatial & environmental data
  • Healthcare data
  • Medical birth registry
  • Mortality data
  • Other government data
  • Police & judicial system data
  • Tax, income & benefit data
Features

Engagement

  • None
  • Keywords

    Disease prevalence
    Environmental factors
    Health and wellbeing
    Health behaviour
    Healthcare access and use
    Lifestyle
    Occupational exposure
    Population health
    Quality of life
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