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临床试验/NCT00078767
NCT00078767已完成3 期

Pharmacologic Treatment of PTSD in Sexually Abused Children

Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2001年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
24
试验地点
1
主要终点
Kiddie-Sads-Present and Lifetime (KSADS-PL) Scale for PTSD

研究概览

简要总结

This study will evaluate the benefit of adding sertraline (Zoloft®) to Trauma-Focused Cognitive Behavioral Therapy (TF-CBT) for sexually abused children who have Posttraumatic Stress Disorder (PTSD).

详细描述

Adult research has demonstrated the efficacy of selective serotonin reuptake inhibitors (SSRIs) in decreasing Posttraumatic Stress Disorder (PTSD) symptoms; to date the SSRIs are the only medication class with demonstrated efficacy in treating all three PTSD symptom clusters (reexperiencing, avoidance, and hyperarousal). No studies have evaluated the impact of SSRIs on PTSD symptoms in children or adolescents. Trauma-focused CBT has been shown in several studies to be efficacious in decreasing PTSD symptoms in sexually abused children and adolescents. Many children and youth with PTSD are currently prescribed SSRIs and other medications. This study will evaluate whether adding the SSRI sertraline provides additional benefits over TF-CBT treatment for sexually abused children and adolescents with PTSD. If adequate numbers of children with comorbid PTSD and depressive and/or anxiety disorders are included, it may also be possible to evaluate whether any benefit of adding sertraline is restricted to those children with comorbid disorders.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
10 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

TF-CBT + sertraline

Experimental

Trauma-Focused CBT provided individually to youth and parent for 12 sessions (90 minute sessions; 45 minutes for youth; 45 minutes for parent); plus Sertraline provided in dosage titrated as clinically indicated by child psychiatrist blind to treatment assignment, from 50mg/day to a maximum dosage of 150 mg/day

干预措施: Trauma-Focused Cognitive Behavioral Therapy (Behavioral)

TF-CBT + sertraline

Experimental

Trauma-Focused CBT provided individually to youth and parent for 12 sessions (90 minute sessions; 45 minutes for youth; 45 minutes for parent); plus Sertraline provided in dosage titrated as clinically indicated by child psychiatrist blind to treatment assignment, from 50mg/day to a maximum dosage of 150 mg/day

干预措施: Sertraline Pill (Drug)

TF-CBT +placebo

Active Comparator

Trauma-Focused CBT provided individually to youth and parent for 12 sessions (90 minute sessions; 45 minutes for youth; 45 minutes for parent); plus placebo identical to Sertraline, provided in pill form and titrated as clinically indicated by child psychiatrist blind to treatment assignment, from 1 to 3 pills/day (identical in appearance to 50 to 150mg/day of Sertraline)

干预措施: Sertraline Pill (Drug)

TF-CBT +placebo

Active Comparator

Trauma-Focused CBT provided individually to youth and parent for 12 sessions (90 minute sessions; 45 minutes for youth; 45 minutes for parent); plus placebo identical to Sertraline, provided in pill form and titrated as clinically indicated by child psychiatrist blind to treatment assignment, from 1 to 3 pills/day (identical in appearance to 50 to 150mg/day of Sertraline)

干预措施: Placebo Oral Tablet (Drug)

结局指标

主要结局

Kiddie-Sads-Present and Lifetime (KSADS-PL) Scale for PTSD

时间窗: Up to 39 months

Change in PTSD parameters as determined by changes in score. At enrollment, participants either did or did not have a PTSD diagnosis. The three categories displayed show participants who had the PTSD diagnosis at the time of enrollment but did have evidence of PTSD at the end of their participation, participants who had PTSD at enrollment and who continued to exhibit PTSD at the end of their participation, and those who did not have a PTSD diagnosis at the start of the trial. There are numerous criteria used to determine a PTSD diagnosis; they are not individually listed. The diagnosis was sufficient for the purposes of the study.

次要结局

  • Mood and Feelings Questionnaire (MFQ) for Depressive Symptoms(Up to 39 months)
  • Anxiety Symptoms(Up to 39 months)
  • Incidence of Suicidality(Up to 39 months)
  • Global Impairment(Up to 39 months)

研究者

发起方
Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)
申办方类型
Other
责任方
Principal Investigator
主要研究者

Judith Cohen

Principle Investigator

Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)

研究点 (1)

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