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临床试验/NCT00607412
NCT00607412已完成2 期

AUDs and PTSD Treatment for Victims of Partner Violence

University of California, San Diego2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2007年8月最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
50
试验地点
2
主要终点
CAPS for PTSD symptoms and ASI for substance use

研究概览

简要总结

The goal of this study is to evaluate a psychotherapy for PTSD and substance use disorders among women who have experienced domestic violence. The hypothesis is that women who receive present-focused, integrated treatment will have greater PTSD symptom reduction and have less substance use after treatment than women in the control condition who will receive supportive therapy based on a 12-step approach.

详细描述

The goal of this study is to evaluate an integrated psychotherapy for PTSD and substance use disorders among female victims of intimate partner violence. The hypothesis is that women who receive present-focused, integrated treatment will have greater PTSD symptom reduction and have less substance use post-treatment than women in the control condition who will receive supportive therapy based on a 12-step approach.

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
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • female victims of partner violence
  • at least one month out of the abusive relationship
  • meet DSM-IV (American Psychiatric Association, 1994) criteria for PTSD and an alcohol use disorder
  • literate in English
  • have not changed psychotropic medications or dosages within the past two months and agree not to during the active phase (first 12 weeks) of the intervention
  • have an identified primary care physician

排除标准

  • moderate or severe cognitive impairment as measured by a Mini-Mental State Examination score less than or equal to 18
  • Histories of psychosis or mania may be excluded because the presence of these disorders is thought to impede progress in psychotherapy

结局指标

主要结局

CAPS for PTSD symptoms and ASI for substance use

时间窗: pre, mid treatment, post, 3-month follow-up, 6-month follow-up

次要结局

  • Timeline Follow-back procedure, Beck Depression Inventory(same as primary)

研究者

申办方类型
Other

研究点 (2)

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