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Netherlands Study of Depression and Anxiety (NESDA)
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Sample details

NESDA is a longitudinal, multi-site, naturalistic, case-control cohort study following a sample of around 3,000 participants with and without depressive and/or anxiety disorders from the Netherlands. The original NESDA sample of 2,981 participants (2,329 individuals with and 652 individuals without a lifetime diagnosis of depressive and/or anxiety disorders) were recruited from the community, primary care practices and specialised mental health institutions in the regions of Amsterdam and Leiden, and in the provinces of Groningen, Drenthe and Friesland. The sample were initially assessed at baseline between 2004 and 2007, and subsequently followed up for 13 years with 7 waves of extensive assessments. At the 9-year follow-up (wave 6), the study recruited additional participants who were siblings of 256 original NESDA participants with a lifetime anxiety and/or depressive disorder.

Study design
Cohort

Number of participants at first data collection

2,981 (participants)

Age at first data collection

18 - 65 years (participants)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Control participants
Patients and clinical populations
Dataset details

Country

Netherlands

Year of first data collection

2004

Primary Institutions

Amsterdam University Medical Center (Amsterdam UMC)

Leiden University Medical Center (Leids Universitair Medisch Centrum, LUMC)

University Medical Center Groningen (Universitair Medisch Centrum Groningen, UMCG)

Links

nesda.nl/

doi.org/10.1002/mpr.256

Funders

Geestelijke Gezondheidszorg Drenthe (GGZ Drenthe)

Geestelijke Gezondheidszorg Friesland (GGZ Friesland)

Geestelijke Gezondheidszorg Rivierduinen (GGZ Rivierduinen)

Geestelijke Gezondheidszorg inGeest (GGZ inGeest)

Leiden University Medical Center (LUMC)

Ongoing?
Yes

Data types collected

neuroImagingData
mentalHealthData
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)
  • Secondary data
  • Self-report questionnaire – online
  • Self-report questionnaire – paper or computer assisted
  • Wearable devices
Qualitative data collection
  • None
Neuroimaging data collection
  • Functional magnetic resonance imaging (fMRI)
Linked or secondary data
  • Healthcare data
Features

Engagement

  • Community engagement
  • Keywords

    Anxiety
    Biological samples/biospecimens
    Biomarkers
    Comorbidity
    Depression
    Epidemiology
    Genetic predisposition
    Health and wellbeing
    Health behaviour
    Healthcare access and use
    Mental health
    Personality
    Prognosis
    Psychiatry
    Psychosocial factors
    Social conditions and environment

    Consortia and dataset groups

    Amsterdam Cohort Hub
    Geoscience and health cohort consortium (GECCO)
    Lifebrain
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