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Clinical Trials/NCT03195829
NCT03195829
Completed
N/A

A Computerized Cognitive Stimulation Program in Elderly With Mild Cognitive Impairment: A Feasibility Study

Leila DJABELKHIR0 sites20 target enrollmentDecember 2015

Overview

Phase
N/A
Intervention
Not specified
Conditions
Mild Cognitive Impairment, So Stated
Sponsor
Leila DJABELKHIR
Enrollment
20
Primary Endpoint
GROBER-BUSCHKE TEST
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

This non-pharmacological interventional feasibility study evaluate a computerized cognitive stimulation program in elderly with mild cognitive impairment.

Detailed Description

Involvement in social and leisure activities has been associated with a decreased risk of dementia in the elderly with Mild Cognitive Impairment (MCI). MCI is a crucial phase to prevent the worsening of cognitive decline in elderly at risk to develop dementia. These last years, the use of computerized training programs to enhance cognitive functioning showed positive and promising results. However, the effects on psychosocial factors still poorly documented in cognitive interventions in MCI. It seems essential to promote these factors involving social ties, group dynamic, the motivation, as factors that can contribute to enhance social life and cognitive functioning. This feasibility study evaluated a computer-based cognitive stimulation in elderly with MCI and explore the effects on cognitive and psychosocial components.

Registry
clinicaltrials.gov
Start Date
December 2015
End Date
July 2016
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

Neuropsychologist

Broca Hospital

Eligibility Criteria

Inclusion Criteria

  • Clinical diagnosis of Mild Cognitive Impairment
  • Absence of history of alcohol or other substance consumption
  • No engagement in other cognitive intervention program

Exclusion Criteria

  • Psychiatric and neurological disorders
  • Conversion toward dementia during intervention
  • Sensory and or motor deficit that could interfere with the use of computer tool

Outcomes

Primary Outcomes

GROBER-BUSCHKE TEST

Time Frame: Baseline assessment before intervention, change from baseline at 3 months immediately after intervention

Assessment of free and cued recall of episodic memory

Secondary Outcomes

  • Technologies Acceptation Questionnaire(Baseline assessment before intervention, change from baseline at 3 months immediately after intervention)

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