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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ANZCTR |
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Last refreshed on:
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22 February 2013 |
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Main ID: |
ACTRN12611000702910 |
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Date of registration:
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08/07/2011 |
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Primary sponsor: |
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Public title:
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Cognitive and neural benefits of brain training.
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Scientific title:
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Double-blind, randomised clinical trial timecourse changes in response to computerised cognitive training compared to active control training in a group of cognitively healthy older adults, as measured with a battery of cognitive tests and MRI scans. |
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Date of first enrolment:
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28/06/2011 |
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Target sample size:
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80 |
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Recruitment status: |
Closed: follow-up continuing |
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URL:
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http://www.anzctr.org.au/ACTRN12611000702910.aspx |
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Study type:
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Interventional |
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Study design:
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Randomised controlled trial
Parallel |
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Countries of recruitment
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Australia
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Contacts
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Name:
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Mr Mr Amit Lampit |
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Address:
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Regenerative Neuroscience Group
Brain and Mind Research Institute
University of Sydney
100 Mallet St
Camperdown NSW 2050, Australia
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Telephone:
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+61 9114 4134 |
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Email:
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amit.lampit@sydney.edu.au |
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Affiliation:
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Name:
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A/Prof Dr Michael Valenzuela |
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Address:
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Regenerative Neuroscience Group
Brain and Mind Research Institute
University of Sydney
100 Mallet St
Camperdown NSW 2050, Australia
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Telephone:
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+61 2 9114 4135 |
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Email:
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michael.valenzuela@sydney.edu.au |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion criteria: (1) Non-demented, non-depressed older adults; (2) physical ability to attend brain training sessions 3 times a week
Exclusion criteria: (1) history, diagnosis or treatment for dementia (of any aetiology); (2) diagnosis or treatment for depression in last 6 months; (3) history of stroke in last 12 months; (4) major neurological disorder requiring current treatment (epilepsy); (5) major psychiatric disorder requiring current treatment (schizophrenia, bipolar disorder); (6) physical (sensory or motor) impairment that would limit ability to engage with training; (7) lack of personal informant who sees the person at least once a week; (8) current undertaking of any other Brain Training program; (9) current alcohol abuse.
Age minimum:
65 Years
Age maximum:
0 No limit
Gender:
Both males and females
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Health Condition(s) or Problem(s) studied
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Neuroplasticity in the cognitively healthy elderly
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Intervention(s)
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26 exercises from the COGPACK package, a suite of exercises that are largely based upon well-established neuropsychological tests and principles. Multiple exercises will be used to target the one generic cognitive domain and exercises will include both verbal and visual modalities. Training will be administered in three 1-hour sessions every week for a total period of 12 weeks (i.e. a total of 36 hours), supervised by a member of the research team.
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Primary Outcome(s)
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Scores in (1) A subset of tests taken from Mindstreams: Verbal Memory, Non Verbal Memory, Staged Information Processing Speed, Stroop Interference; (2) "Stockings of Cambridge," a problem solving test from the CANTAB.
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Scores in (1)a computer-based adaptation of WAIS 4 Matrix Reasoning test; (2) Controlled Oral Word Association Test (COWAT); (3) the Boston Naming Test (short versions) and (4) a computerised adaptation of the Recognition Memory Test.
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Secondary Outcome(s)
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(1) Structural plasticity: T1-weighted isometric 3D scan; (2) Biochemical plasticity: Magnetic resonance spectroscopic analysis of metabolites in both the hippocampus and posterior cingulate; (3) Functional plasticity: resting state fMRI scan; and (4) White matter plasticity: Diffusion Tractography Imaging. These outcomes collected on a subsample of n=15 subjects.
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Bayer Instrumental Activities of Daily Living (B-ADL)
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Source(s) of Monetary Support
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Primary Dementia Collaborative Research Centre
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