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Cooperative Health Research in South Tyrol study (CHRIS study)
Cooperative Health Research in South Tyrol study logo
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Sample details

The CHRIS cohort is an ongoing population-based study investigating genetic and lifestyle determinants of health and healthy aging in a cohort of 13,393 adults from the Val Venosta/Vinschgau district of South Tyrol, Italy. From 2011 to 2018, participants aged 18 years and older completed baseline assessments providing biological samples and a wide range of sociodemographic, behavioural, and clinical information, with a focus on cardiovascular, metabolic, neurologic, and psychiatric health. The first follow-up phase began in 2019 and is anticipated to continue until 2027. As of 2025, over 5,500 participants have completed a visit as part of ongoing follow-up, providing most of the same data and samples as at baseline. The CHRIS cohort includes 667 participants who previously took part in the Microisolates in South Tyrol (MICROS) study in 2002/3, thereby providing additional longitudinal data and biological samples for these participants.

Study design
Cohort, Biobank

Number of participants at first data collection

13,393 (participants)

Age at first data collection

18 - 94 years (participants)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Adults
Alpine
Older and elderly people
Population-based sample
Rural populations
Dataset details

Country

Italy

Year of first data collection

2011

Primary Institutions

Eurac Research Institute for Biomedicine

Healthcare System of the Autonomous Province of Bolzano-South Tyrol

Links

chris.eurac.edu/

eurac.edu/en/institutes-centers/institute-for-biomedicine/pages/chris

doi.org/10.1186/s12967-015-0704-9

chrisportal.eurac.edu/

eurac.edu/chrisack

Profile paper DOI

doi.org/10.1093/ije/dyaf064

Funders

Department of Innovation, Research, University and Museums of the Autonomous Province of Bolzano-South Tyrol

European Regional Development Fund (ERDF)

Ongoing?
Yes

Data types collected

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
  • None
Linked or secondary data
  • Existing research data
Features

Engagement

  • Participant or community advisory groups
  • Community engagement
  • Keywords

    Biological samples/biospecimens
    Biomarkers
    Cardiovascular health and disease
    Cognitive assessments
    Genetics
    Health and wellbeing
    Lifestyle
    Mental health
    Metabolomics
    Neurology and neurological diseases
    Neuropsychiatric assessment
    Physical health assessments
    Proteomics
    Psychiatry
    Sleep

    Consortia and dataset groups

    Biobank Standardisation and Harmonisation for Research Excellence in the European Union (BioSHaRE-EU)
    Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE)
    DIAbetes Gentetics Replication and Meta-analysis (DIAGRAM)
    Genetic Investigation of Anthropometric Traits (GIANT)
    Thyroidomics Consortium
    Type 2 Diabetes Global Genetics Initiative (T2DGGI)
    Ygen consortium
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