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临床试验/NCT05640882
NCT05640882尚未招募不适用

Is Olfaction the Key to PTSD

Bar-Ilan University, Israel0 个研究点目标入组 1,000 人开始时间: 2023年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
1,000
主要终点
PTSD Status

研究概览

简要总结

Participants arriving to the ED following a potentially traumatic event such as a motor vehicle accident will be recruited into the study. Inclusion criteria: aged 18-65, Hebrew as a first language, no current psychiatric disorder. Exclusion criteria: loss of consciousness, unable to understand study procedure. Participants will answer self report questionnaires in the ED. They will be invited for a follow up interview 2 weeks and six months post trauma. Between 2 weeks and 6 months they will be folllowed up via online questionnaires. At the interviews, they will encounter 20 different olfactory stimuli, answer self-report questionnaires, and a clinical interview assessing Axis 1 disorders and PTSD will be completed. At six month, participants with PTSD will be offered therapy in the embedded RCT. Patients will receive VRET (Virtual reality exposure therapy) with or without olfaction.

详细描述

The goal of this project is to carry out a systematic longitudinal study with an embedded RCT examining olfactory memories in PTSD, in order to test the following hypotheses. Firstly, olfactory memories occur after all traumatic events; secondly, olfactory memories are predictors of PTSD development and thirdly, adding olfaction to PTSD treatment will enhance treatment outcome. The project comprises of a longitudinal study recruiting participants in the Emergency Room within hours of a traumatic event, assessing them at two weeks post trauma for olfactory memories, and at six months for PTSD. This will allow the first two hypotheses to be examined. Participants with PTSD and olfactory memories will be offered treatment and will be randomized to a Virtual Reality Exposure Therapy with and without added odors. Post treatment assessments will examine the third hypothesis.

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
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • hebrew native speaker
  • understand study requirements

排除标准

  • current psychiatric disorder
  • suicidality

结局指标

主要结局

PTSD Status

时间窗: 3 months after end of treatment

PTSD diagnosis as measured by the CAPS

PTSD Levels

时间窗: 3 months after end of treatment

PTSD Symptoms Levels as measured by the CAPS continuous score

次要结局

未报告次要终点

研究者

发起方
Bar-Ilan University, Israel
申办方类型
Other
责任方
Principal Investigator
主要研究者

Sara Freedman

prof.

Bar-Ilan University, Israel

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