跳至主要内容
临床试验/NCT01904799
NCT01904799
已完成
不适用

Cognitive Assessment for Stroke Patients: Reproductibility and Validity Study

Centre Hospitalier Universitaire Dijon1 个研究点 分布在 1 个国家目标入组 263 人2015年1月2日
适应症Stroke

概览

阶段
不适用
干预措施
Cognitive Assessment test
疾病 / 适应症
Stroke
发起方
Centre Hospitalier Universitaire Dijon
入组人数
263
试验地点
1
主要终点
test of visual memory
状态
已完成
最后更新
2个月前

概览

简要总结

After a CVA, all of the cognitive functions can be affected and analysed, but the presence of a language disorder may considerably hamper the evaluation of other functions.

The battery of rapid tests to screen for and quantify cognitive disorders, including the MMSE, the MOCA, the R-CAMCOG or the RBANS, are not suitable for aphasic patients because they contain items with a strictly verbal response. Because of this, inexperienced doctors cannot evaluate higher functions (other than language) of aphasics in routine practice. For the same reason, aphasics are regularly excluded from post-cva therapeutic protocols, whether or not the trial bears on the evolution of cognitive functions.

Nonetheless, it is possible to evaluate, at least roughly, all of the cognitive functions without resorting to language.

The investigator have developed , from validated tests and classical clinical manoeuvers, the Cognitive Assessment for Stroke Patients (CASP) :

  • for the rapid screening (less than 15 minutes) and quantification of post-cva cognitive disorders (6 functions: language, apraxia, short-term memory, temporal orientation, impaired spatial/visio-construction and executive functions);
  • the CASP can be used in most patients, including those with severe disorders of expression and moderate problems with comprehension, The format of these tests has been adapted so that severe disorders of expression (essentially left-hemisphere CVA), and left spatial impairment (right-hemisphere CVA) do not affect the ability to take the test. Its validity in terms of appearance and content were verified in 2011.
注册库
clinicaltrials.gov
开始日期
2015年1月2日
结束日期
2019年3月29日
最后更新
2个月前
研究类型
Interventional
研究设计
Single Group
性别
All

研究者

入排标准

入选标准

  • For CVA patients
  • patients hospitalised in rehabilitation after a first recent hemispheric CVA (less than 6 weeks) ;
  • aged \> 18;
  • absence of severe disorders of oral comprehension (BDAE aphasia severity score \>2 for comprehension);
  • whatever the severity of oral expression disorders;
  • who have been given clear written and oral information, and after the doctor has verified their ability to understand the protocol.
  • For " Control " patients (to evaluate divergent validity)
  • patients hospitalised in rehabilitation units or geriatrics taking part in this study;
  • aged \> 18.

排除标准

  • For CVA patients
  • patients who do not speak French;
  • cognitive disorders known before the CVA;
  • psychotic disorders known before the CVA;
  • major visual disorders incompatible with reading, known before the CVA.
  • For " Control " patients (to evaluate divergent validity)
  • patients who do not speak French;
  • cognitive disorders known before the CVA;
  • psychotic disorders known before the CVA;
  • major visual disorders incompatible with reading, known before the CVA.

研究组 & 干预措施

Cognitive Assessment

干预措施: Cognitive Assessment test

结局指标

主要结局

test of visual memory

时间窗: Evaluation at 6 ± 2 weeks

comprehensive assessment battery of higher functions

时间窗: Evaluation at 6 ± 2 weeks

comprehensive assessment battery of higher functions

时间窗: baseline

comprehensive assessment battery of higher functions

时间窗: Evaluation at 3 ±1 days

test of visual memory

时间窗: baseline

test of visual memory

时间窗: Evaluation at 3 ±1 days

研究点 (1)

Loading locations...

相似试验