跳至主要内容
临床试验/NCT00552006
NCT00552006已完成不适用

A Randomized Controlled Clinical Trial (RCCT) to Test the Effectiveness of Narrative Exposure Therapy (NET) Versus an Attention Control Condition (AC) in Reducing Trauma Related Symptoms in Formerly Abducted Children and Former Child Soldiers Suffering From Posttraumatic Stress Disorder (PTSD)

University of Konstanz1 个研究点 分布在 1 个国家目标入组 85 人开始时间: 2007年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
85
试验地点
1
主要终点
Load of traumatic symptoms measured via the CAPS (Clinician-administered PTSD scale)

研究概览

简要总结

In the aftermath of traumatic experiences like natural disasters or man-caused traumatic events, such as war experiences, a substantial part of the affected individuals develop a number of psychological symptoms. The characteristic symptom pattern occurring in the aftermath of traumatic events is called posttraumatic stress disorder (PTSD) and includes functional impairment of the affected individuals. The investigators want to test whether Narrative Exposure Therapy (NET) is an effective tool in reducing trauma related symptoms in formerly abducted children and youths and former child soldiers, when applied by lay personnel.

研究设计

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

入排标准

年龄范围
12 Years 至 25 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • clinical diagnosis of PTSD (Post-Traumatic Stress Disorder) derived from expert interviews
  • member of the group of formerly abducted people or former child soldiers

排除标准

  • current substance dependence
  • mental retardation
  • psychotic disorder

结局指标

主要结局

Load of traumatic symptoms measured via the CAPS (Clinician-administered PTSD scale)

时间窗: 3 months, 6 months and 1 year after completion of treatment

次要结局

  • Load of depressive symptoms measured via the MINI, strength of suicidal ideation measured via the MINI, functionality measured via the CAPS, feelings of guilt measured via the CAPS, stigmatization measured via an adapted version of the PSQ(3 months, 6 months and 1 year after completion of treatment)

研究者

发起方
University of Konstanz
申办方类型
Other

研究点 (1)

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