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Clinical Trials/NL-OMON54855
NL-OMON54855
Recruiting
Not Applicable

Intervention for mood disorder symptoms in children of parents with psychiatric disorders - the MARIO intervention study - the MARIO intervention study

Erasmus MC, Universitair Medisch Centrum Rotterdam0 sites340 target enrollmentTBD
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Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Erasmus MC, Universitair Medisch Centrum Rotterdam
Enrollment
340
Status
Recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • •\- Participation in the niet\-WMO study (\*Vroege herkenning van
  • •stemmingsstoornissen bij kinderen van ouders met psychiatrische stoornissen \-
  • •de MARIO\-screening studie\*) including consent to be contacted again for future
  • •\- Child has a parent with a psychiatric disorder, based on parent and/or child
  • •\- Child is in the age range of 10 \- 26 years
  • •\- Written informed consent of child and parent (depending on age of the child)
  • •\- Fluent in Dutch

Exclusion Criteria

  • •\- Current depressive or BD disorder diagnosis and/or suicidality based on the
  • •K\-SADS psychiatric interview that was conducted in the telephone interview as
  • •part of the online MARIO\-screening study (METC number: 2019\.486\). However, in
  • •case of a mild current depressive episode during the MARIO\-screening study, we
  • •will ask participants who gave permission for future studies if they agree on
  • •another K\-SADS psychiatric interview (on mood symptoms and suicidality) after a
  • •period of 6 months. If they agree, and there is no current mood episode
  • •according to the K\-SADS psychiatric interview, the participant is able to
  • •participate in the MARIO Intervention study.
  • •\- Not having adequate access to laptop or mobile phone during the study period.

Outcomes

Primary Outcomes

Not specified

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