Neuropsychological Factors Associated With Vulnerability to Suicidal Behavior in Depressed Elderly Patients (SPAD)
研究概览
地位
条件
详细说明
The secondary objectives are to confirm or explore the deficits of certain cognitive processes involved in potentially suicidal behavior in depressed elderly persons but that have been little or not studied to date. These include:
A. cognitive control and sensitivity to interference (Victoria Stroop test, incompatibility test, flexibility test, Go / No-Go);
B. Strategic recovery of semantic memory (verbal fluency test);
C. Working memory (TEA);
D. Insight related to depression (Mood Disorders Insight Scale);
E. Recognition of facial emotions;
F. Emotional regulation;
G. Negative attitudes;
H. Self-perception and;
I. Time perspectives.
Finally, patients will be contacted by telephone at month 6 to assess the occurrence of a suicidal act during this period and thus calculate the predictive ability of cognitive and psychological factors.
研究类型
注册 (实际的)
联系人和位置
学习地点
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Nîmes、法国、30000
- Clinique Les Sophoras
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Nîmes Cedex 09、法国、30029
- CHRU de Nîmes - Hôpital Universitaire Carémeau
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
研究人群
描述
Inclusion criteria for patients:
- The patient or his/her representative must have given his/her informed and signed consent
- The patient must be insured or beneficiary of a health insurance plan
- Patients with a diagnosis of current, moderate to severe, major depressive episode according to the DSM diagnostic criteria 5. This episode can be considered as part of a major depressive disorder or bipolar disorder.
- Patients with or without a personal history of suicide attempts. A suicide attempt is defined as any act performed with some intent to die (Mann 1998). Suicidal threats, aborted or interrupted gestures as well as self-mutilating acts without suicidal intent will not be considered as suicidal acts.
- Patients hospitalized (or followed as outpatients) in the Nîmes University Hospital psychiatry department or the Sophoras clinic in Nimes
Inclusion criteria for healthy subjects:
- The subject or his/her representative must have given his/her informed and signed consent
- The subject must be insured or beneficiary of a health insurance plan
- Non-depressed subject without personal history of lifetime mood disorder or severe mental illness, or substance or alcohol abuse during the past 12 months
Exclusion criteria for patients:
- The patient is participating in another study
- The patient is in an exclusion period determined by a previous study
- The patient is under judicial protection
- The patient (or his/her legal representative) refuses to sign the consent
- It is impossible to correctly inform the patient or his/her legal representative
- The patient has a known MMSE score <24 (elimination of probable dementia pathology)
- Known central neurological disease including degenerative disease, severe head trauma and severe cerebral vascular disease
- Known schizophrenia and other psychotic disorders
- Alcohol or substance abuse in the last 12 months
- Electroconvulsive therapy in the 12 months preceding the study because of the risk of mnesic side effects
- Inability to perform neuropsychological tests because of a language problem, poor understanding, a major tremor, inability to sit still, a major sight problem that can not be corrected, or other severe cognitive impairment
- The subject presents an acute somatic decompensation incompatible with the completion of this study
- The patient has current confusion
Exclusion criteria for healthy subjects:
- The subject is participating in another study
- The subject is in an exclusion period determined by a previous study
- The subject is under judicial protection
- The subject (or his/her legal representative) refuses to sign the consent
- It is impossible to correctly inform the subject or his/her legal representative
- The subject has a known MMSE score <24 (elimination of probable dementia pathology)
- Known central neurological disease including degenerative disease, severe head trauma and severe cerebral vascular disease
- Known schizophrenia and other psychotic disorders
- Alcohol or substance abuse in the last 12 months
- Electroconvulsive therapy in the 12 months preceding the study because of the risk of mnesic side effects
- Inability to perform neuropsychological tests because of a language problem, poor understanding, a major tremor, inability to sit still, a major sight problem that can not be corrected, or other severe cognitive impairment
- The subject has a mood disorder
- The subject presents an acute somatic decompensation incompatible with the completion of this study
- Thesubject has current confusion
Pharmacological treatment is not a criterion for exclusion in itself but it will be left to the judgment of the evaluator to choose to include a subject or not (or to postpone inclusion) depending on the drug (eg. after weaning daytime sedative treatment and benzodiazepines).
学习计划
研究是如何设计的?
设计细节
队列和干预
团体/队列 |
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Major depressive episode
This study population consists of patients over 60 years of age with or without a personal history of suicide attempts, hospitalized in the Nîmes University Hospital psychiatry department or the Sophoras clinic for a major depressive episode.
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Healthy subjects
Healthy subjects over 60 years, not depressed and without personal history of severe mental illness or suicide attempts will be recruited.
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研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
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Trust Game
大体时间:Days 1-7
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Days 1-7
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Ultimatum Game
大体时间:Days 1-7
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Days 1-7
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Iowa Gambling Task
大体时间:Days 1-7
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Days 1-7
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次要结果测量
结果测量 |
大体时间 |
|---|---|
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Stroop Victoria Test
大体时间:Days 1-7
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Days 1-7
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Incompatibility Test
大体时间:Days 1-7
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Days 1-7
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Flexibility test
大体时间:Days 1-7
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Days 1-7
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Go-NoGo
大体时间:Days 1-7
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Days 1-7
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Working memory - TEA
大体时间:Days 1-7
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Days 1-7
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Mood Disorders Insight Scale
大体时间:Days 1-7
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Days 1-7
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Verbal fluency test
大体时间:Days 1-7
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Days 1-7
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Future autobiographical fluency task
大体时间:Days 1-7
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Days 1-7
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Bristol Emotion Recognition Test
大体时间:Days 1-7
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Days 1-7
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Cognitive Emotion Regulation Questionnaire
大体时间:Days 1-7
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Days 1-7
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Questionnaire on negative attitudes towards problems
大体时间:Days 1-7
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Days 1-7
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Revised self-awareness scale, Self-reference task
大体时间:Days 1-7
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Days 1-7
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Balanced Temporal Perspective Scale
大体时间:Days 1-7
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Days 1-7
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Suicide attempt within 6 months of follow-up
大体时间:Month 6
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Month 6
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合作者和调查者
调查人员
- 研究主任:Fabrice JOLLANT, MD、Centre Hospitalier Universitaire de Nîmes
出版物和有用的链接
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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