Dementia - Subcortical |
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Clinical Trial: Cognitive Training in the Elderly
This study is currently recruiting patients.
Verified by Beersheva Mental Health Center September 2005
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Purpose
Background The aging of the population has lead to a significant increase in the number of older people suffering from cognitive impairment and dementia. The present lack of effective drug therapy for these conditions makes it imperative to investigate other potential therapeutic interventions.
Cognitive training has been described as possibly useful in improving cognitive function in elderly subjects with mild impairment and early dementia. However, there have been few well-designed studies to date and the results are equivocal. Most studies have relied on the use of paper-based neuropsychological assessment instruments with limited accuracy and reproducibility. We have developed a validated computerized neuropsychological assessment battery with increased test-retest reliability.
The purpose of this study is to assess the efficacy of a computerized training program on cognitive function in older persons with normal cognition, mild cognitive impairment, and early dementia.
Description A randomized prospective AB/BA cross-over study. Methods Eligible males and females aged 60 years and older following initial computerized neuropsychological assessment will be randomized to receive either a 12-session computerized cognitive training program, or no treatment. Repeat neuropsychological assessment will be followed by a 4-week no treatment phase, reassessment and crossover phase. Repeat assessments will be performed at three and six months.
| Condition | Intervention |
|---|---|
| mild cognitive impairment and dementia | Behavior: computerized cognitive training |
MedlinePlus consumer health information
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Placebo Control, Crossover Assignment
Official Title: The Effect of Computerized Cognitive Training on Neuropsychological Measures of Cognitive Function in the Elderly.
Expected Total Enrollment: 300
Study start: September 2005; Expected completion: June 2007
Eligibility
Accepts Healthy Volunteers
Inclusion Criteria:
- age: above 60
Exclusion Criteria:
- visual impairment
- educational inability to perform training
Location and Contact Information
Yaacov Grinshpun, MD 972-8-6401520 yaacovg@bgu.ac.il
Israel
Beersheva Mental Health Center, Beersheva, Israel; Recruiting
Tzvi Dwolatzky, MD, Principal Investigator
Tzvi Dwolatzky, MD, Principal Investigator, Ben Gurion University of the Negev
More Information
Last Updated: September 6, 2005
Record first received: September 4, 2005
ClinicalTrials.gov Identifier: NCT00146263
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration
ClinicalTrials.gov processed this record on 2005-09-13

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