跳至主要内容
临床试验/NCT00001486
NCT00001486
已完成
不适用

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

National Institute of Mental Health (NIMH)1 个研究点 分布在 1 个国家目标入组 4,914 人1995年7月15日

概览

阶段
不适用
干预措施
Parents
疾病 / 适应症
Schizoaffective Disorder
发起方
National Institute of Mental Health (NIMH)
入组人数
4914
试验地点
1
主要终点
Genetic Polymorphisms affect phenotypes
状态
已完成
最后更新
4天前

概览

简要总结

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.

详细描述

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.

注册库
clinicaltrials.gov
开始日期
1995年7月15日
结束日期
待定
最后更新
4天前
研究类型
Observational
性别
All

研究者

入排标准

入选标准

  • INCLUSION/

排除标准

  • 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.
  • Exclusion Criteria for Siblings (probands and unaffected siblings):
  • Seizure disorder, mental retardation, organic brain damage or other neurological disease.
  • History of any (excepting nicotine-related) DSM5-defined moderate to severe substance use disorder (or DSM-IV-defined substance dependence).
  • Cumulative lifetime history of any (excepting nicotine-related) DSM5-defined mild substance use disorder (or any DSM-IV-defined substance abuse), either in excess of 5 years total or not in remission for at least 6 months.

研究组 & 干预措施

Parents

Parents of Probands and siblings for the purposes of DNA collection

Normal Controls

Male and female adult healthy volunteers

Probands

Adult Subjects with Schizophrenia Spectrum Disorders

Siblings

Adult siblings of Probands

结局指标

主要结局

Genetic Polymorphisms affect phenotypes

时间窗: At time of study participation

genotyping analysis

次要结局

  • PANSS, AIMS, GAF(At time of study participation)

研究点 (1)

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