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RecruitingMild Cognitive Impairment

EVASION: Effect of VisuAl Stimulation on attentION

Eligible age

60+ yrs

Accepts

All genders

Locations

0 states

Healthy volunteers

No

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About this study

The main objective is to compare changes in information processing speed after 30 days of intervention in participants with a dysexecutive mild cognitive impairment (MCI) and receiving either cognitive stimulation by adapted visual exercises (Emeraude® software) or the broadcasting of a television program without cognitive stimulation. Secondary objectives are: * To compare, after 30 days of intervention, in participants with a dysexecutive MCI and receiving either cognitive stimulation by adapted visual exercises (Emeraude® software), or the broadcasting of a television program without cognitive stimulation : * changes in information processing speed of each subtest, * changes in cognitive performance, * changes in executive functions, * changes in walking performance. * To compare the quality of life, after 30 days of intervention, of participants with a dysexecutive MCI and receiving either cognitive stimulation by adapted visual exercises (Emeraude® software) or the broadcasting of a television program without cognitive stimulation. * In the "Intervention" group, to study correlations between changes in information processing speed index and the final level reached for each cognitive stimulation exercise.

Sponsor: University Hospital, Angers

You may qualify if…

  • Age ≥ 60 years
  • Diagnosis of mild cognitive impairment of a dysexecutive or multidomain dysexecutive nature, according to Winblad consensus criteria
  • Presence of an informal caregiver
  • Subject gave and signed informed consent to participate in the study
  • Affiliation to a social security scheme

You may not qualify if…

  • Presence of severe depressive symptoms (4-item Geriatric Depression Scale score \> 2)
  • Ophthalmological or central pathology that may affect the performance of stimulation exercises
  • Regular use of psychotropic drugs that may have an impact on the performance of stimulation exercises, in the opinion of the investigator (benzodiazepines, antidepressants, neuroleptics, hypnotics)
  • Use of anticonvulsant drugs
  • Existence of a confusional syndrome
  • Participation in another simultaneous clinical trial
  • Person deprived of liberty by judicial or administrative decision
  • Person under forced psychiatric care

Source: ClinicalTrials.gov · NCT05791994 · last updated 2026-04-06