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临床试验/NCT06470893
NCT06470893已完成不适用

Online Exposure Therapy for Obsessive-Compulsive Disorder (OCD) Study

University of Miami2 个研究点 分布在 1 个国家目标入组 63 人开始时间: 2024年9月23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
63
试验地点
2
主要终点
Change in OCD Symptoms Measured by Yale-Brown Obsessive Compulsive Scale-Second Edition (YBOCS-II)

研究概览

简要总结

The overarching goal of this protocol is to investigate mechanisms that influence symptom outcomes of exposure and response prevention (ERP) therapy for OCD. Mechanisms may include affective processes, learning factors, cognitive factors, or other constructs that could influence treatment outcomes. The study team will conduct this research within the context of an effective online treatment for OCD called OCD-NET. OCD-NET is bibliotherapy with coaching and its content is reflective of standard care for OCD.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • English-speaking
  • Located within the United States
  • 18-90 years old
  • Able to provide consent
  • Current diagnosis of OCD as assessed by clinical interview

排除标准

  • Adults unable to consent
  • Individuals who are not yet adults (infants, children, teenagers)
  • Participants currently located outside of the United States
  • Prisoners
  • Participants with hoarding as the primary OCD symptom
  • Severe mental illness (e.g. schizophrenia, substance abuse); organic brain syndrome; or serious, current suicidal/homicidal ideation (based on phone screening or initial assessment)
  • Concurrent enrollment in another psychotherapy treatment
  • Participants taking psychotropic medication may be excluded if:
  • They have started a brand new psychotropic medication within the last 12 weeks
  • They have changed the dose of their psychotropic medication within the last 4 weeks
  • They anticipate that they cannot maintain the current dose of their psychotropic medication for the duration of the study
  • Participants may be excluded if they have any cognitive or physical impairments that would interfere with their participation (e.g., significant head injury, cognitive disability, dementia).

结局指标

主要结局

Change in OCD Symptoms Measured by Yale-Brown Obsessive Compulsive Scale-Second Edition (YBOCS-II)

时间窗: Baseline, up to 12 months (end of treatment)

YBOCS-II scores range from 0-50, and higher scores indicate more severe illness

次要结局

未报告次要终点

研究者

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

Kiara Timpano

Professor

University of Miami

研究点 (2)

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