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临床试验/jRCT1030250720
jRCT1030250720招募中不适用

Development and Preliminary Evaluation of the Efficacy and Safety of Video-Assisted Group Cognitive Behavioral Therapy for Obsessive-Compulsive Disorder (VOCT)

未提供0 个研究点目标入组 15 人开始时间: 待定
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
15

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Single Arm Study

入排标准

年龄范围
18age old over 至 65age old under(—)
性别
All

入选标准

  • Age 18 or older at the time of consent acquisition
  • Diagnosed with obsessive-compulsive disorder by a primary physician and currently undergoing treatment
  • Permission to participate in this study is obtained from the primary physician
  • Able to respond to interviews online
  • Understands the purpose and content of this study and provides written informed consent to participate voluntarily
  • Consent to not share the program and its materials developed by the research team with others
  • Aged 18 years or older and 65 years or younger at the time of consent acquisition
  • Currently receiving outpatient treatment at this hospital for a diagnosis of obsessive-compulsive disorder
  • Y-BOCS-SR score of 8 points or higher
  • Has obtained permission from their primary physician to participate in this study
  • Understands the purpose and content of this study and has provided written informed consent to participate voluntarily

排除标准

  • Individuals deemed unsuitable for this study by the principal investigator
  • Individuals exhibiting significant suicidal ideation at the pre-intervention assessment stage
  • Individuals exhibiting significant manic episodes at the pre-intervention assessment stage
  • Individuals for whom weekly attendance during the intervention period is known to be difficult in advance
  • Individuals scheduled to receive other structured psychotherapy (excluding supportive therapy) during the intervention period
  • Individuals with physical illness or severe cognitive impairment at the pre-intervention assessment point that would make participation in group cognitive behavioral therapy difficult
  • Individuals who received treatment with structured psychotherapy, modified electroconvulsive therapy, or transcranial magnetic stimulation (excluding medication) within 3 months prior to the pre-intervention assessment.
  • Individuals with difficulty accessing the internet or operating basic digital devices.
  • Other individuals deemed unsuitable for this study by the principal investigator.

研究者

发起方
未提供

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