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临床试验/NCT01435512
NCT01435512已完成不适用

Strength At Home: Veterans' Program (Formerly: Post-Traumatic Stress Disorder (PTSD)-Focused Therapy for Anger and Relationship Conflict Among Operation Enduring Freedom/Operation Iraqi Freedom (OEF/OIF) Veterans)

Boston VA Research Institute, Inc.2 个研究点 分布在 1 个国家目标入组 135 人开始时间: 2009年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
135
试验地点
2
主要终点
Intimate Partner Aggression as Measured by the Conflict Tactics Scale

研究概览

简要总结

This is a research study funded by the Department of Defense to test a therapeutic intervention for male combat veterans who engage in intimate partner violence (IPV). The investigators hope to decrease the recurrence of relationship aggression and help veterans manage anger. The primary aim of the study is to test the intervention.

详细描述

The purpose of this project is to develop, standardize, and test an intervention for combat veterans exposed to trauma who engage in intimate partner aggression (IPA). This intervention, formerly labeled PTSD-Focused Cognitive Behavior Therapy for Partner Violence (PFCBT), and currently called the Strength at Home, Veteran's Program, incorporates components of interventions for IPA and trauma and will target mechanisms implicated in the relationship between trauma and IPA. This project addresses a number of the research gaps in this area of research including: (a) the development of a novel treatment approach to improve functioning and well-being of affected individuals; (b) tertiary prevention (of repeated IPA) during re-integration; and (c) examination of the efficacy of a program providing support for the families and caregivers of veterans with combat history.

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
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Any era veteran
  • Over the age of 18
  • In a relationship within a female partner within the last 6 months
  • At least one act of male-to-female physical aggression over the previous 6 months or at least one act of male-to-female severe violence in the past 12 months
  • Male participant must consent for partner contact

排除标准

  • Participant evidences severe organicity or active psychosis
  • Reading difficulties prevent valid completion of the assessment instruments
  • Participant expresses prominent suicidal or homicidal ideation
  • Participant meets diagnostic criteria for alcohol and/or drug dependence, if not in early full remission or sustained partial remission

研究组 & 干预措施

Group

Experimental

PTSD-Focused Cognitive Behavioral Therapy for Partner Violence

干预措施: PTSD-Focused CBT for Partner Violence (Behavioral)

Waitlist

No Intervention

Control group - no intervention

结局指标

主要结局

Intimate Partner Aggression as Measured by the Conflict Tactics Scale

时间窗: Pretreatment (baseline), Posttreatment (12 weeks), 3 month follow up (24 weeks)

Revised Conflict Tactics Scale-2 (CTS2). The CTS2 is the most widely used measure of IPV, with excellent internal consistency reliability, content validity, and construct validity.76,88 Combined partner reports will be used such that scores of partners who report a greater frequency of specific CTS2 behaviors will be used in analyses to reduce the impact of response biases and the underreporting of abuse. The CTS2 will also be given every four weeks during the course of active intervention. Scale response options range from 0 to 7. Higher overall scores mean more conflict.

次要结局

  • Multidimensional Measure of Emotional Abuse (MMEA)(Pretreatment (baseline), Posttreatment (12 weeks), 3 month follow up (24 weeks))
  • Trait Anger as Measured by the State-Trait Anger Expression Inventory (STAXI) and Aggression as Measured by the Aggression Questionnaire(6-month follow up (72 weeks))
  • Symptoms of Posttraumatic Stress Disorder as Assessed by the Clinician Administered PTSD Scale (CAPS) and the Posttraumatic Stress Disorder Checklist (PCL)(6 month follow-up (72 weeks))
  • Relationship Satisfaction as Measured by the Dyadic Adjustment Scale(6-month follow up (72 weeks))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Casey Taft

Principal Investigator

Boston VA Research Institute, Inc.

研究点 (2)

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