跳至主要内容
临床试验/NL-OMON51843
NL-OMON51843招募中不适用

Effectiveness of a Brief Intensive Trauma Treatment for adolescents with (subclinical) PTSD: a multi-center randomized controlled trial - Effect of a BITT for adolescents with (s)PTSD: a multi-center RCT

Amsterdam UMC0 个研究点目标入组 85 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
85

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
12 至 17(—)

入选标准

  • - 12-18 years of age;
  • - With a history of psychological trauma (conform the Life Events Checklist of
  • the Clinician Administered PTSD Scale for Children and Adolescents DSM-5
  • - At least subthreshold PTSD criteria, conform the CAPS-CA DSM-5, i.e.:
  • o fully meeting criterion A, F and G and at least one symptom of criteria B, C,
  • o or fully meeting criterion A, F, G and at least the B, C, D or E symptom
  • - A written informed consent must be provided by the adolescent and, for
  • adolescents aged 12-15 years, all legal guardians.

排除标准

  • - unable to speak and write Dutch;
  • - estimated or determined mental retardation (IQ <70);
  • - suffering from ongoing trauma by a parent who is part of the adolescent*s
  • current primary-care system.

研究者

发起方
Amsterdam UMC

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