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临床试验/NCT02901769
NCT02901769Unknown不适用

Emotional Prosody Recognition and Decision Making Inf fMRI and Vulnerability to Suicide

Rennes University Hospital2 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2013年2月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
80
试验地点
2
主要终点
fMRI activation area

研究概览

简要总结

Suicide is known to be frequent in depression, and in most of the psychiatric diseases. But as it can occur in patients with no psychiatric illness and doesn't occur in every patients with psychiatric illness, it has to be considered henceforth as a specific vulnerability.

This trial will study two fMRI paradigms, emotional prosody recognition and decision making, in order to characterize emotional and cognitive trait factors in a population of patients vulnerable to suicide. Four different groups will be constituted : depressed suicide attempters, depressed patients with past history of suicidal acts, depressed patients with no history of suicidal acts and healthy controls.

The main goal will be to correlate fMRI activation during the two paradigms in subjects vulnerable to suicide. The secondary goals will be to characterize emotional and cognitive trait factors in these subjects, to demonstrate that those characteristics are independent from depression and to correlate these trait factors with socio-demographic and clinical features with fMRI activations.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Right-handed,
  • Depressed suicide attempters for the first group,
  • Depressed patients with past history of suicidal acts for the second group,
  • Depressed patients with no history of suicidal acts for the third group,
  • Healthy controls for the fourth group.

排除标准

  • Another psychiatric trouble than depression,
  • Another psychotrope treatment than SSRI/SNRI and/or benzodiazepine at inclusion and/or one month before,
  • For the first and secand groups : more than fous suicidals acts within the past 3 years,
  • Deficits that do not allow test realisation (visual audition troubles, cognitif deficits,
  • Prosopagnosia,
  • Pregnancy,
  • Severe central nervous system disease or somatic disease,
  • MRI contra-indication,
  • Major benefiting from a legal protective measure,
  • No coverage care.

结局指标

主要结局

fMRI activation area

时间窗: 1 day

次要结局

未报告次要终点

研究者

发起方
Rennes University Hospital
申办方类型
Other
责任方
Sponsor

研究点 (2)

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