Computer-Based Training for Cognitive Enhancement: Classroom Study
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Details and patient eligibility
About
The primary objective of this study is to evaluate the design and effectiveness of a computer-based training program on the memory and cognitive abilities of mature individuals undergoing healthy aging.
Full description
The purpose of this study is to test the new progressions design of a computer-based training program and to demonstrate the effectiveness of this refined cognitive training regimen on participants' performance on normed neuropsychological measures.
Subjects meeting eligibility criteria and providing written, informed consent will complete 40 one hour sessions of a computer based training program.
Enrollment
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Volunteers
Inclusion criteria
A)Participants must be at least 60 years old B)Participants must have a Mini-Mental State Exam (MMSE) score of 24 or higher to ensure that participants do not meet common criteria for dementia C)Participants must be a native English speaker D)Participants must be able to see well enough to read the consent form E)Participants must be able to hear well enough to understand ordinary spoken conversation when the clinical specialist holds a paper in front of his or her face to prevent the participant from lip-reading.
F)Participants must be willing to commit to the time requirements of the study and not have any scheduled trips or absences for more than 1 week during the training.
Exclusion criteria
A)Participants must not be planning to begin cholinesterase inhibitor (AChEI) therapy or to change their dosing levels. Subjects currently using AChEI will be included if they have an established steady dosing history at least one month prior to the study and are expected to continue at the same dosage throughout the study.
B)Participants must not have had a head trauma that caused them to lose consciousness in the past five years and have had no subsequent symptoms.
C)Participants must not have had a stroke within the past year; or have had a stroke that has left them with expressive or receptive language problems.
D)Participants must not have any central nervous system disorder that could contribute to cognitive impairment.
E)Participants must not have a tremor preventing the use of a computer mouse or other pointing device.
F)Participants must not currently be active in another clinical trial.
Trial design
Primary purpose
Allocation
Interventional model
Masking
94 participants in 3 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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