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临床试验/NCT06102096
NCT06102096已完成不适用

A Randomized Controlled Trial of a Culturally Adapted iCBT for Arabic-speaking Refugee Youth With Common Mental Health Problems

Karolinska Institutet1 个研究点 分布在 1 个国家目标入组 125 人开始时间: 2023年11月27日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
125
试验地点
1
主要终点
HSCL-25

研究概览

简要总结

The aim of the current study is to explore whether culturally adapted internet-based cognitive behavioral therapy is effective in reducing the symptoms of various common mental health problems among Arabic-speaking refugee and migrant youth. We hypothesize that the symptoms of the psychological problems will significantly be reduced among youth who will receive iCBT compared to youth in the control group.

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
15 Years 至 29 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Between the ages of 15 and
  • A score above the cut-off 1.75 on HSCL-25
  • Has a refugee or migrant background
  • Has a good and stable internet connection
  • Has access to a computer, a tablet or a smartphone
  • Is fluent in reading and writing Arabic
  • Has the ability to dedicate time to take part in the intervention for 6-10 weeks.

排除标准

  • Is suffering from a severe mental illness, such as psychosis or severe depression.
  • Is suffering from substance abuse
  • Is undergoing a psychological treatment
  • Has a high risk of suicide

结局指标

主要结局

HSCL-25

时间窗: Pre-intervention, during the intervention, immediately after the intervention, 6 months after completion of the intervention

Assessment of anxiety and depressive symptoms

次要结局

  • PSYCHLOPS(Pre-intervention, immediately after the intervention, 6 months after completion of the intervention)
  • ISI(Pre-intervention, immediately after the intervention, 6 months after completion of the intervention)
  • BRS(Pre-intervention, immediately after the intervention, 6 months after completion of the intervention)
  • PG-13(Pre-intervention, immediately after the intervention, 6 months after completion of the intervention)
  • PCL-5(Pre-intervention, immediately after the intervention, 6 months after completion of the intervention)
  • WHO-5(Pre-intervention, immediately after the intervention, 6 months after completion of the intervention)
  • PHQ-9(Pre-intervention, immediately after the intervention, 6 months after completion of the intervention)

研究者

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

Shervin Shahnavaz

PhD Lecturer

Karolinska Institutet

研究点 (1)

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