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临床试验/NCT00736346
NCT00736346Unknown不适用

Efficacy of Three Treatment Modalities for Panic Disorder Among Individuals Consulting Emergency Departments for Non Cardiac Chest Pain

Université du Québec a Montréal3 个研究点 分布在 1 个国家目标入组 204 人开始时间: 2005年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
发起方
入组人数
204
试验地点
3
主要终点
Panic Disorder diagnosis

研究概览

简要总结

The purpose of this study is to assess the impact of three different treatment modalities on panic symptoms, quality of life and use of health services among individuals consulting an emergency department for non cardiac chest pain and having Panic Disorder.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Aged 18 and over
  • Mastered oral and written French
  • Consulted an emergency department for chest pain with very low risk of coronary disease (normal ECG and blood tests)
  • Met criteria for Panic Disorder

排除标准

  • Chest pain with an obvious medical origin (obvious trauma or abnormal pulmonary x-rays)
  • Had received cognitive-behavior therapy for Panic Disorder in the last six months
  • Cognitive impairment preventing the completion of psychological assessment
  • Past or present psychotic episode, Bipolar Disorder, or organic mental disorder
  • Current Abuse or Dependence Disorder
  • If another Mental Disorder is present, its severity was equal or inferior to the severity of Panic Disorder
  • Current medical condition preventing the participant from receiving pharmacological of cognitive-behavior treatment

研究组 & 干预措施

1

Active Comparator

干预措施: Brief cognitive-behavioral treatment for Panic Disorder (Behavioral)

2

Active Comparator

干预措施: Cognitive-Behavior Therapy for Panic Disorder (Behavioral)

3

Active Comparator

干预措施: paroxetine (Drug)

结局指标

主要结局

Panic Disorder diagnosis

时间窗: Pre and posttreatment, and 3, 6 and 12 months after treament

次要结局

  • Panic symptomatology, psychological distress, quality of life, and use of health services(Pre and posttreatment, and 3, 6 and 12 months after treatment)

研究者

发起方
Université du Québec a Montréal
申办方类型
Other

研究点 (3)

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