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Genetic Study of Schizophrenia

A Neurobiological Investigation of Patients With Schizophrenia Spectrum Disorders and Their Siblings

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00001486
Enrollment
4914
Registered
1999-11-04
Start date
1995-07-15
Completion date
Unknown
Last updated
2026-09-16

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

Conditions

Schizoaffective Disorder, Schizophrenia

Keywords

Negative Symptoms, Brain Scans, Hallucinations, Delusions, Psychosis and Schizophrenia, Natural History

Brief summary

This large ongoing study at NIMH investigates the neurobiology of schizophrenia by identifying susceptibility genes, evaluating their impact on brain function to better understand how to treat and prevent this illness....

Detailed description

Objective: Schizophrenia is a complex genetic disorder which likely involves many genes each producing a slight increase in risk. Finding weak-acting genes in complex genetic disorders has been challenging and will likely require a number of approaches and large clinical samples. Several strategies have emerged recently that appear to markedly improve the power of genetic studies for detecting such genes. These include using association (rather than linkage) and using intermediate phenotypes in addition to DMS-IV diagnosis. Study Population: We propose to take advantage of these techniques by studying quantitative traits related to schizophrenia in patients, siblings, and controls. Design: We will employ an association design, rather than linkage. Traits will include quantifiable neurobiological variables that have been implicated previously as possible phenotypes related to schizophrenia. These include tests of attention and cognition. Outcome Measure: We will use several statistical methods to show that specific genetic polymorphisms affect these phenotypes, including case control and family based association studies.

Interventions

None listed

Sponsors

National Institute of Mental Health (NIMH)
Lead SponsorNIH
National Institutes of Health Clinical Center (CC)
CollaboratorNIH

Study design

Observational model
CASE_CONTROL
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* INCLUSION/

Exclusion criteria

Inclusion criteria for Siblings (probands and unaffected siblings): * Probands must have a DSM IV-R diagnosis of schizophrenia,schizoaffective disorder, psychosis N.O.S. or schizophreniform disorder. * Probands and Siblings must be between the ages of 18 and 55 * Probands and Siblings must be free of major medical illnesses, but may have controlled hypertension, thyroid disease, or diabetes. * Probands and Siblings must have the cognitive ability to consent for themselves. Those who are judged to have the cognitive ability to consent for themselves at the time of participation, but do not have the legal capacity to consent for themselves may participate if the legal guardian /Legal authorized representative (LAR) provides consent by signing the informed consent form. * Fluency in English is required.

Design outcomes

Primary

MeasureTime frameDescription
Genetic Polymorphisms affect phenotypesAt time of study participationgenotyping analysis

Secondary

MeasureTime frameDescription
PANSS, AIMS, GAFAt time of study participationPANSS, AIMS, GAF

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORKaren F Berman, M.D.

National Institute of Mental Health (NIMH)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 17, 2026