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Preventing mood and anxiety disorders in youth: a multicentre prevention trial in the high risk offspring of depressed and anxious patients

Preventing mood and anxiety disorders in youth: a multicentre prevention trial in the high risk offspring of depressed and anxious patients - Offspring of parents with mood and anxiety disorders

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON33876
Enrollment
204
Registered
2009-11-24
Start date
2009-11-24
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

depressieve symptomen anxiety and depression / mood disorder / affective disorders

Interventions

Children are randomized to one of two treatment conditions, namely (a) 10 weekly individual child CBT sessions and 2 parent sessions. The following themes will be addressed: emphasizing the child*s

Sponsors

Rijksuniversiteit Groningen
Lead Sponsor

Eligibility

Age
2 Years to 17 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria (parents): at least one of the biological parents is currently being treated for a depression (MDD, dysthymia) or an anxiety disorder (Social phobia SocP, Agoraphobia AP, Panic disorder PD, Generalized anxiety disorder GAD, Separation anxiety disorder SAD); informed consent. Inclusion criteria (offspring): age 8-18; being at risk for developing a depression or anxiety disorder, defined as meeting at least 2 of the 3 criteria of the High Risk Index (risk factors: female sex, 2 affected parents, suicide attempt of one of the parents; see Ch. 1) or reporting subthreshold symptoms of anxiety or depression, defined as scoring above the 80th percentile of the RCADS questionnaire (we chose a relatively high cutoff value for the RCADS, to enhance specificity); informed consent.

Exclusion criteria

Exclusion criteria: Exclusion criteria (both parents): mental retardation; index parent is not fluent in Dutch; severe alcohol or substance use disorder; schizophrenia or other primary psychotic disorder; schizoaffective disorder; bipolar disorder BPD, Obsessive-compulsive disorder OCD, PTSD, only simple phobia SP. Exclusion criteria (offspring): mental retardation; not speaking Dutch fluently; severe alcohol or substance use disorder; current diagnosis of MDD, dysthymia, SocP, AP, PD, GAD, BPD, PTSD, OCD, SP; previous or current treatment for a DSM-IV psychiatric disorder.

Design outcomes

Primary

MeasureTime frame
Primary outcome is the time to onset of depression or anxiety disorder in the offspring.

Secondary

MeasureTime frame
Secondary outcome measures include number of days with depression or anxiety, child and parent symptoms, quality of life, and cost-effectiveness. In line with models on aetiology of mood and anxiety disorders as well as mechanisms of change during interventions, we selected possible mediators of treatment outcome, namely attribution style, coping, parent-child interaction and attachment, personality, optimism and self-esteem.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)