跳至主要内容
临床试验/NCT00481000
NCT00481000Unknown2 期

Dialectical Cognitive Traumatherapy (DCT) on Patients With Severe Posttraumatic Stress Disorder Following Sexual Abuse - A Randomised Controlled Trial

Central Institute of Mental Health, Mannheim2 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2007年4月1日最近更新:
适应症

试验速览

阶段
2 期
发起方
入组人数
64
试验地点
2
主要终点
PTSD Symptoms (CAPS, SCID, PDS, IESR)

研究概览

简要总结

The purpose of this study is to determine whether Dialectical Cognitive Traumatherapy is effective in the treatment of severe and chronic Posttraumatic Stress Disorder (PTSD) following childhood sexual abuse.

详细描述

Most studies on psychological treatments for PTSD exclude patients with severe, co-occurring psychopathology. We designed a new treatment (Dialectical Cognitive Trauma Therapy, or DCT) specifically to treat these patients. DCT includes elements of emotion regulation, mindfulness exercises, cognitive and exposure treatment, as well as new elements. This randomized controlled study evaluates the effect of inpatient DCT on these patients.

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
None

入排标准

年龄范围
17 Years 至 —(Child, Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Minimum age of 17
  • Childhood sexual abuse
  • Posttraumatic Stress Disorder (criteria of SCID)
  • At least one of the following diagnoses: Anorexia Nervosa, or Bulimia Nervosa, or substance abuse, or substance dependence, or major depression or at least 4 out of 9 criteria for Borderline Personality Disorder

排除标准

  • Diagnosis of schizophrenia
  • Mental retardation
  • Body Mass Index lower than 16.5
  • Acute delirium
  • Perilous selfharming behaviour during the last 4 month
  • Suicide attempt with the distinct intention to die during the last 4 month
  • Unstability (e.g. homelessness, acute victimisation by offender)
  • Pretreatment by DCT

结局指标

主要结局

PTSD Symptoms (CAPS, SCID, PDS, IESR)

时间窗: 1.5 years

次要结局

  • general psychopathology(1.5 years)
  • change of pain threshold(1.5 years)
  • fMRI: activity of the amygdala(6 months)

研究者

发起方
Central Institute of Mental Health, Mannheim
申办方类型
Other

研究点 (2)

Loading locations...

相似试验