Skip to main content
Clinical Trials/NCT00319943
NCT00319943
Completed
Phase 1

Computer-Based Therapy for Mild Cognitive Impairment

Posit Science Corporation1 site in 1 country48 target enrollmentSeptember 2004

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Mild Cognitive Impairment
Sponsor
Posit Science Corporation
Enrollment
48
Locations
1
Primary Endpoint
The study investigates changes in a neuropsychological assessment battery pre-randomization
Status
Completed
Last Updated
20 years ago

Overview

Brief Summary

The purpose of this study is to determine the neuropsychological and neurophysiological impacts of a computer-based training program designed to improve the cognitive performance of patients with mild cognitive impairment (MCI).

Detailed Description

The study is a randomized, double-blind, controlled trial of a computerized, cognitive intervention with three main goals: 1) to assess the magnitude of improvements in memory, language function, and cognitive function following computer training, 2) to investigate the neurophysiological mechanisms underlying such neuropsychological improvements, and 3) to demonstrate the feasibility of using this kind of computer-based therapy in older populations.

Registry
clinicaltrials.gov
Start Date
September 2004
End Date
July 2006
Last Updated
20 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 65 - 90 years of age 2)Meet definition for MCI including complaints of cognitive decline as indicated by patient report and/or informant report, and corroborated by clinician judgment and, the absence of dementia, defined as impairment of memory and at least one other domain of cognitive function.
  • Fluency in English 4)Willing to meet the time commitment of the study

Exclusion Criteria

  • Clinically significant cerebrovascular disease
  • Individuals scheduled to begin acetylcholinesterase inhibitor (AChEI) therapy -

Outcomes

Primary Outcomes

The study investigates changes in a neuropsychological assessment battery pre-randomization

and upon the completion of training.

Secondary Outcomes

  • Early evaluations will be conducted from brain imaging; specifically, date
  • obtained via positron emission tomography (PET), magnetoencephalography (MEG),
  • electroencephalography (EEG), and functional magnetic resonance imaging (fMRI)
  • studies.

Study Sites (1)

Loading locations...

Similar Trials