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KUNO-Kids Birth Cohort Study
KUNO-Kids Birth Cohort Study logo
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Sample details

The KUNO-Kids birth cohort study was established to investigate various aspects of child health, using novel omics technologies in a systems medicine approach. After 3 years of recruitment, 2,515 infants and their families have joined the study, which is based in Eastern Bavaria in Regensburg, Germany. KUNO-Kids aims to investigate a wide range of exposures and outcomes. Data are collected not only from the index child (or children in the case of multiples), but also from his/her family. The inclusion in the study starts immediately after birth of the index child. The baseline assessment takes place during the short hospital stay of the mother and child directly after birth. Regular follow-up assessments are conducted when the index child is 4 weeks old, 6 months old, and at each birthday. At baseline, the mothers’ mean age was 33.9 years, and 56% gave birth for the first time.

Study design
Cohort - birth, Cohort - primary caregiver and child

Number of participants at first data collection

2,515 (families)

Age at first data collection

≥ 18 years (mothers)

Birth (children)

Varied (fathers)

Participant year of birth

Varied (mothers)

2015 - 2020 (children)

Varied (fathers)

Participant sex
All

Representative sample at baseline?
No

Sample features

Families
Newborns, infants and babies
Dataset details

Country

Germany

Year of first data collection

2015

Primary Institutions

University of Regensburg (Universität Regensburg)

Links

kunokids.info/

Funders

European Union (EU)

Federal Ministry of Education and Research (Bundesministerium für Bildung und Forschung, BMBF) now known as Federal Ministry of Research, Technology and Space (Bundesministerium für Forschung, Technologie und Raumfahrt, BMFTR)

University Children’s Hospital of the University of Regensburg

Ongoing?
Yes

Data types collected

Quantitative data collection
  • Interview – face-to-face
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Self-report questionnaire – paper or computer assisted
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • None
Features

Engagement

  • Community engagement
  • Keywords

    Anthropometry
    Biological samples/biospecimens
    Diet and nutrition
    Human development
    Infant biosamples
    Physical health
    Pregnancy outcomes
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