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Mood and Resilience in Offspring (MARIO)
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Sample details

MARIO is an observational, longitudinal cohort study in offspring of parents with a mood disorder and offspring of controls, aged between 10 and 25 years in the Netherlands. Offspring were recruited from existing patient studies. During this 3-year longitudinal study, data are collected at 4 time points (baseline (T0), 1 year (T1), 2 years (T2), and 3 years (T3) after baseline). Over this period of three years, extensive clinical, biological, and environmental data and data on risk and resilience are collected through various methods, including blood sampling, face-to-face interviews, online questionnaires, actigraphy, and experience sampling method assessment.

Study design
Cohort

Number of participants at first data collection

~450 (participants)

~100 (controls)

Recruitment is ongoing

Age at first data collection

10 - 25 years (participants)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Adolescents
Children and young people
Control participants
Young adults
Dataset details

Country

Netherlands

Year of first data collection

2020

Primary Institutions

Erasmus University Medical Centre (Erasmus MC)

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

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

University Medical Center Utrecht (Universitair Medisch Centrum Utrecht, UMCU)

VU University Medical Center (VU Medisch Centrum, VUmc)

Links

mario-project.nl/

erasmusmc-rdo.nl/project/mario-mood-and-resilience-in-offspring-project/

Funders

The Netherlands Organisation for Health Research and Development (ZonMW)

Ongoing?
Yes

Data types collected

mentalHealthData
dataLinkage
Quantitative data collection
  • Activity log (e.g. food, sleep, exercise)
  • Computer, paper or task testing (e.g. cognitive testing, theory of mind doll task, attention computer tasks)
  • Interview – face-to-face
  • Interview – phone
  • Passive electronic data collection (e.g. screen time, scroll speed)
  • 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

  • Patients, service users, lived experience involvement
  • Participant or community advisory groups
  • Community engagement
  • Keywords

    Biological determinants
    Biological samples/biospecimens
    Clinical risk
    Environmental factors
    Genetics
    Human development
    Intergenerational
    Mental health
    Mood disorders
    Parental mental health
    Resilience
    Risk factors

    Consortia and dataset groups

    FAMILY Consortium
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