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临床试验/NCT00998569
NCT00998569已完成不适用

Neurocognitive Enhancement in Major Depressive Disorder

Queen's University2 个研究点 分布在 1 个国家目标入组 33 人开始时间: 2009年10月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
33
试验地点
2
主要终点
Performance on paper and pencil assessments of neurocognition after treatment, compared to baseline assessment performance

研究概览

简要总结

The purpose of this study is to examine the effects of neurocognitive enhancement on cognitive abilities and related social and adaptive behaviours in individuals diagnosed with major depressive disorder. Subjects in this study will be randomized to receive Neurocognitive Enhancement Therapy (NET) or to a wait list and then NET . Secondary aims include examining whether the cognitive benefits are potentiated by repeated exposure during in-home practice with complementary exercises. Additionally, the investigators will examine the durability of the effects and their generalization to functional capacity and everyday functional performance after completion of the groups.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male or Female.
  • Subjects will be between the ages of 18 and 65, which is the age range with available normative comparison data.

排除标准

  • Presence of a medical diagnosis that is associated with known cognitive impairments, such as multiple sclerosis, cerebrovascular accident, dementia, or history of traumatic brain injury.
  • Subjects with a reading level below grade 6, as assessed with the Wide Range Achievement Test - Reading Recognition Subtest, will be excluded because of the likelihood of not understanding task instructions.
  • Subjects with uncorrectable vision or hearing impairment that would preclude valid assessments or intervention procedures.

结局指标

主要结局

Performance on paper and pencil assessments of neurocognition after treatment, compared to baseline assessment performance

时间窗: 20 weeks

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Christopher Bowie

Ph.D.

Queen's University

研究点 (2)

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