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Gene Environment interactions in Mental health trajectorieS of Youth (Youth-GEMS)

Gene Environment interactions in Mental health trajectorieS of Youth (Youth-GEMS) - Youth-GEMS

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON57257
Enrollment
175
Registered
2024-04-16
Start date
2025-05-20
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Young people between the age of 12-24 years, accessing outpatient specialized mental health services for the first time "Mental health problems" and "mental health disorders" Mental health problems

Interventions

None listed

Sponsors

Universiteit Maastricht
Lead Sponsor

Eligibility

Age
12 Years to 64 Years

Inclusion criteria

Inclusion criteria: • Age between 12-24 years. • New appointment with a mental health service within the past two months • Good command of the languages used in the study. • Written informed consent by the participant, their parents if minors, or  legal representatives if appropriate.

Exclusion criteria

Exclusion criteria: • Previous contact with a mental health service at the same level of care (primary, secondary, tertiary, quaternary) within the past 12 months.- Intellectual disability with associated functional impairment. • Severe neurological or medical condition. • Genetically confirmed neurobehavioral syndromes.  • Participants that exhibit significant difficulties to complete the  self-reported questionnaires or those whose genetic or biological analysis  confirm an underlying health or genetic condition will be excluded.

Design outcomes

Primary

MeasureTime frame
The main outcome will be overall mental health measured with MyLifeTracker. This is a scale that consists of five items targeting areas of importance to youth: general well-being, day-to-day activities, relationships with friends, relationships with family, and general coping.

Secondary

MeasureTime frame
Secondary outcomes include the following areas: clinical, cognition, self-reported assessment, digital phenotyping, and biological data. Participants can be asked to participate in subparts of the study. Among others, a qualitative study will be performed to retrieve more insight into the lived experience of participants. Additionally, a subgroup will use 'experience sampling method'. For all subparts, participants will be asked to give additional informed consent.

Countries

Netherlands

Contacts

Public ContactZ.I.J. Rutten

Universiteit Maastricht

sp-youthgems@maastrichtuniversity.nl0614348173

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Aug 9, 2026