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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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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT00611312 |
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Date of registration:
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28/01/2008 |
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Primary sponsor: |
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Public title:
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Effects of Delivery Mode of Cognition Intervention in Early Alzheimer's Disease
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Scientific title:
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Effects of Intense Cognitive Training on Standardized Measures of Cognition in Those With Very Mild Alzheimer's Disease |
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Date of first enrolment:
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February 2008 |
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Target sample size:
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25 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT00611312 |
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Study type:
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Interventional |
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Study design:
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Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care
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Countries of recruitment
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United States
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Contacts
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Name:
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Yvonne Colgrove, PhD, PT |
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Address:
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Telephone:
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Email:
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Affiliation:
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University of Kansas |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Diagnosis of very mild Alzheimer's Disease (CDC of 0.5) and mild Alzheimer's Disease
(CDC of 1.0)
Exclusion Criteria:
- Neurologic disorder other than Alzheimer's disease
Age minimum:
60 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Alzheimer's Disease
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Intervention(s)
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Behavioral: Cognitive Training
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Primary Outcome(s)
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Composite score of 5 cognitive tests including 1)WAIS digit span, 2) word fluency, 3) trail making test-A 4) Rey Osterrieth complex figure and 5) MMSE
[Time Frame: 2 weeks with FU at 2 and 4 months]
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Secondary Outcome(s)
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Brain activity during functional brain imaging
[Time Frame: 2 weeks]
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Secondary ID(s)
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11008
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IIRG-07-57789
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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