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Not yet recruiting NCT06874075

Psychiatric Disorders in Child and Adolescent Offspring of Parents with Schizophrenia and Bipolar Disorders.

Observational Mood Disorders Schizophrenia Disorders

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Mood Disorders, Schizophrenia Disorders. Basic parameters: 6 years — 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Offspring of parents with bipolar disorder (BD) and schizophrenia (SZ) are vulnerable and at high risk for these disorders. Despite the fact that positive family history of SZ or BD is the strongest predictor for the development of these severe mental illnesses, there is limited evidence assessing young adults of SZ and BP simultaneously with lack of detailed handling of similarities in risk and developmental trajectories during adolescence

Detailed description

Offspring of parents with bipolar disorder (BD) and schizophrenia (SZ) are vulnerable and at high risk for these disorders. Despite the fact that positive family history of SZ or BD is the strongest predictor for the development of these severe mental illnesses, there is limited evidence assessing young adults of SZ and BP simultaneously with lack of detailed handling of similarities in risk and developmental trajectories during adolescence \[1, 2\]. SZ and BP are thought to share a common pathophysiological basis due to advances in the field of molecular genetics, which have yielded overlapping findings between the two disorders \[3, 4\]. The psychopathological base during adolescence is influenced by neurodevelopmental deviation prior to clinical onset of many severe mental illnesses \[5, 6\]. Moreover, the risk for developing psychopathology is high during adolescence and prodromal symptoms start even earlier and may overlap and are difficult to differentiate \[5-8\]. This has turned efforts towards identification and treatment of individuals at early stages of the illness, when first clinical manifestations emerge \[8, 9\].

Importantly, subthreshold symptoms of mania and depression along with unspecific behavioural, emotional, and cognitive manifestations are highly predictive of future manic and depressive episodes in BD as well as anxiety disorders, which is confirmed by the clinical staging perspective \[10, 11\]. Nevertheless, early recognition and intervention during the prodromal phase is still at an early stage in Sz \[12\] with limited research into valid prodromal criteria for BP \[13\]. Retrospective studies combining subjects with early-onset mania and early-onset first-episode psychosis have reported a similar pattern of neurodevelopmental and psychopathological features predating the appearance of more specific prodromal symptoms in both disorders \[14, 15\]. Therefore, the substantial overlap of symptoms in the initial phases suggests that early identification programmes should be aimed at detecting both the pre-psychotic and the pre-manic phases of SZ and BP \[16\]

Primary outcome measures

  • Early recognition of psychiatric disorders among children and adolescents , So Early interventions to decrease the severity of the disorder can be done [Time frame: 6 months]
Secondary outcome measures (1)
  • overlap of symptoms in the initial phases suggests that early identification [Time frame: 6 months]

Eligibility criteria

Inclusion criteria

\- 6\_18 years IQ > 70 parents of schizophrenia \& mood disorders .

Exclusion criteria

  • age <6 or >18 IQ < 70 .

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Family-based

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06874075 · psychiatric marriage outcome

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗