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Prevalence of Cognitive Disorders in Newly Diagnosed Epilepsy (PRECONISE)

2022年1月11日 更新者:Maillard Louis、Central Hospital, Nancy, France

A prospective prevalence study recorded that up to 50% of adult patients with newly diagnosed epilepsy had at least one cognitive impairment before initiation of antiepileptic drug (AED). Multiple factors exist and interact in the same patient. Cognitive impairments may affect psychiatric (loss of self-esteem, anxiety, depression) and social status (e.g., vocational aptitude, educational). These factors in turn influence cognitive abilities in a triangular and bidirectional relationship. In addition, the type of epilepsy, development in childhood or cerebral ageing, antiepileptic treatments (AED, surgery) and etiology also have an impact on cognitive performances. The burden of these factors differs from patient to another and must be determined individually. Longitudinal follow-up seems to be crucial because it will allow us to highlight the change in the cognitive profile of newly diagnosed patients over time.

The main objective is to compare the prevalence of cognitive impairment in patients with newly diagnosed epilepsy prior to the initiation of AED with healthy subjects matched on age, sex, manual laterality and socio-educational level. But also to compare the longitudinal evolution of the cognitive profile of patients with healthy controls (0 to 10 years) to determine, among the age of onset seizures, their etiology, the syndrome, the sex, the socio-educational level and the cognitive reserve, which one are related to the severity of cognitive disorders.

研究概览

研究类型

观察性的

注册 (预期的)

300

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

16年 及以上 (孩子、成人、年长者)

接受健康志愿者

是的

有资格学习的性别

全部

取样方法

非概率样本

研究人群

Patients are recruited in the neurology department of the hospital of Nancy. Nomal controls are recruited by display in hospital of Nancy.

描述

Inclusion Criteria (patients):

  • Individuals who have received full information about the organization of the research and have not refused to participate and to use their data.
  • Person aged 16 and over
  • For minor patients: the non-opposition of the parental authority holders
  • Newly diagnosed epileptic patient who had never taken antiepileptic drugs.

Inclusion Criteria (normal controls):

  • Individuals who have received full information about the organization of the research and have not refused to participate and to use their data.
  • For minor participants: the non-opposition of the parental authority holders
  • Person aged 16 and over.

Exclusion Criteria (patients):

  • Person of full age who are subject to a legal protection measure or who are unable to express their consent
  • Person with a progressive brain injury
  • Person who regularly use psychoactive substances (cannabis, alcohol, etc.)
  • Patients who started an antiepileptic treatment before the neuropsychological assessment.

Exclusion Criteria (normal controls):

  • Persons of full age who are subject to a legal protection measure or who are unable to express their consent
  • Person with a neurological (traumatic brain injury, stroke, etc.) and/or psychiatric (mental illness, depression, etc.) history.
  • People who regularly use psychoactive substances (cannabis, alcohol, etc.).

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
干预/治疗
Newly diagnosed epileptic patients
Newly diagnosed epileptic patients who have never be treated by antiepileptic drugs and who have no psychiatric (mental illness) and/or evolutive neurological history and for minor patients the non-opposition of the parental authority holders.
Neuropsychological assessement including memory, working memory, executive function, oral naming and speed processing tests. There are questionnaires to assess mood disorders, anxiety and cognitive reserve.
Normal controls
Matched (on age, gender, socio-educationnal level and manual laterality) healthy controls who have no psychiatric (depression, mental illness) and/or neurological (stroke, traumatic brain injury, etc.) history and for minor patients the non-opposition of the parental authority holders.
Neuropsychological assessement including memory, working memory, executive function, oral naming and speed processing tests. There are questionnaires to assess mood disorders, anxiety and cognitive reserve.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
The percentage of impaired cognitive function at the time of diagnosis in patients and healthy subjects.
大体时间:Baseline (up to 2 weeks after a diagnosis of epilepsy for a duration of 1h30)

Neuropsychological assessment:

  • BVMT-R
  • RL/RI-16
  • Digit span forward and backward (WASI-IV)
  • Stroop test
  • Verbal fluency
  • TMT
  • Code
  • Oral naming

Questionnaires:

  • NDDI-E
  • GAD-7
  • Beck inventory
  • STAI
  • CRI-q
Baseline (up to 2 weeks after a diagnosis of epilepsy for a duration of 1h30)

次要结果测量

结果测量
措施说明
大体时间
Proportion of impaired cognitive functions according to the cognitive domain assessed
大体时间:Baseline, 6 months, 12 months, 3 years, 6 years and 10 years after the baseline (for a duration of 1h30 at each assessment)

Participants are assessed 6 times

Neuropsychological assessment:

  • BVMT-R
  • RL/RI-16
  • Digit span forward and backward (WASI-IV)
  • Stroop test
  • Verbal fluency
  • TMT
  • Code
  • Oral naming

Questionnaires:

  • NDDI-E
  • GAD-7
  • Beck inventory
  • STAI
  • CRI-q
Baseline, 6 months, 12 months, 3 years, 6 years and 10 years after the baseline (for a duration of 1h30 at each assessment)

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Louis Maillard, Pr、Professor of Neurology

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2021年2月17日

初级完成 (预期的)

2022年2月17日

研究完成 (预期的)

2026年2月1日

研究注册日期

首次提交

2021年1月21日

首先提交符合 QC 标准的

2021年1月25日

首次发布 (实际的)

2021年1月27日

研究记录更新

最后更新发布 (实际的)

2022年1月26日

上次提交的符合 QC 标准的更新

2022年1月11日

最后验证

2022年1月1日

更多信息

与本研究相关的术语

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研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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