Skip to main content
Clinical Trials/NCT03195803
NCT03195803
Completed
Not Applicable

Evaluation of Differential Effects of a Computer-based-cognitive Intervention on Cognition Among Elderly With Mild Cognitive Impairment With and Without White Matter Hyperintensities: A Comparative Study.

Leila DJABELKHIR0 sites51 target enrollmentOctober 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Mild Cognitive Impairment
Sponsor
Leila DJABELKHIR
Enrollment
51
Primary Endpoint
Rey Auditory Verbal Learning test
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

This is a non-pharmacological study evaluating the differential effects of a computerized cognitive stimulation program according to the existence or not of white matter hyperintensities in elderly with mild cognitive impairment.

Detailed Description

White matter hyperintensities (WMH) are increasingly recognized as a factor determining the heterogeneity of Mild Cognitive Impairment (MCI) and have been associated to executive and processing speed impairment. Cognitive interventions in MCI remain quite limited for these MCI with vascular profile and studies often distinguish patients by clinical subtypes rather than brain profile before an intervention. Considering magnetic resonance imaging (MRI) data, this study investigated the effects of a computer-based cognitive stimulation (CCS) program on MCI with WMH compared to MCI without WMH.

Registry
clinicaltrials.gov
Start Date
October 2015
End Date
April 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Leila DJABELKHIR
Responsible Party
Sponsor Investigator
Principal Investigator

Leila DJABELKHIR

PhD candidate

Broca Hospital

Eligibility Criteria

Inclusion Criteria

  • Clinical diagnosis of Mild Cognitive Impairment
  • With and without white matter hyperintensities
  • MRI available or accept to perform one
  • No engagement in other cognitive intervention program

Exclusion Criteria

  • Psychiatric and neurological disorders
  • History of alcohol or other substance abuse
  • Sensory and/or motor deficit affecting the use of a tablet

Outcomes

Primary Outcomes

Rey Auditory Verbal Learning test

Time Frame: Baseline assessment, change from Baseline on Rey Auditory Verbal Learning test at 3 months immediately after intervention and at 3 months follow-up

Assessment of verbal learning in episodic memory

Similar Trials