JPRN-UMIN000008322已完成1 期
Feasibility Study of Unified Protocol for Anxiety and Depressive Disorders - Open label study of Unified Protocol for Emotional Disorders
ational Center of Neurology and Psychiatry, National Center for Cognitive Behavior Therapy and Research0 个研究点目标入组 17 人开始时间: 2012年7月12日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 17
研究概览
简要总结
The severity of anxiety symptoms decreased significantly after the intervention and remained low for 3 months.
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20years-old 至 65years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1. No alcohol or substance use disorder in 6 months prior to the screening. 2. No history or concurrent manic or psychotic episode. 3. No other primary DSM-IV Axis I Disorders in six months prior to the screening. 4. No comorbid of antisocial personality disorder. 5. No serious suicidal ideation at screening. 6. Evidence of unable to participate half or more of the intervention phase. 7. No past treatment of CBT. 8. No structured psychotherapy (except supportive therapy) during the intervention. 9. No major cognitive deficits at screening. 10. No life-threatening, severe or unstable physical disorders at screening. 11. Other relevant reason decided by the investigators.
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