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临床试验/NCT01206842
NCT01206842已完成不适用

Social Cognition Training in Schizophrenia

Oslo University Hospital2 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2011年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
48
试验地点
2
主要终点
Social cognitive tests

研究概览

简要总结

People with schizophrenia show deficits in social cognition, the ability to process information about other people such as identifying their emotional expressions. Social cognition is associated with everyday life functioning and could therefore be an important treatment target. Several social cognitive training programs have been developed during the last years. Results indicate that social cognitive performance can be ameliorated through commonly used intervention techniques. However, it is less clear whether this improvement generalizes to everyday life. The purpose of this study is to investigate if a social cognitive training program (Training in Affect Recognition) improves performance on social cognitive and neuropsychological tests and leads to improved everyday life functioning in persons with schizophrenia. The study also aims at examining if an improvement is present three months after completion of the training intervention.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment
盲法
Single (Investigator)

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • age 18-55
  • diagnosis of schizophrenia or schizoaffective disorder
  • sufficient mastery of Norwegian to undergo assessments

排除标准

  • history of head trauma
  • neurological/medical condition known to interfere with central nervous system
  • receiving outpatient care at time of recruitment

研究组 & 干预措施

social cognition training

Experimental

干预措施: Training in Affect Recognition (Other)

treatment as usual

No Intervention

结局指标

主要结局

Social cognitive tests

时间窗: Within one week and within three months of completed training

PFA and MASC

次要结局

  • Functional capacity tests(Within one week and within three months of completed training)
  • Neuropsychological tests(Within one week and within three months of completed training)

研究者

发起方
Oslo University Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Anja Vaskinn

PhD

Oslo University Hospital

研究点 (2)

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