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Effects of Delivery Mode of Cognition Intervention in Early Alzheimer's Disease

Phase 2
Completed
Conditions
Alzheimer's Disease
Interventions
Behavioral: Cognitive Training
Registration Number
NCT00611312
Lead Sponsor
University of Kansas
Brief Summary

The purpose of this study is to see if an intense two-week long cognitive training program helps the thinking ability of adults with very mild Alzheimer Disease. We anticipate that scores on clinical cognitive tests will be better after the training.

Detailed Description

Twenty of the 30 subjects will be recruited to participate in functional magnetic resonance imaging (fMRI). Scanning will be done while subjects perform a verbal learning task. Ten subjects will be scanned before and after the two week training. Another ten will be scanned twice at a two week interval before beginning the cognitive training.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
25
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
1Cognitive TrainingCognitive Training
Primary Outcome Measures
NameTimeMethod
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) MMSE2 weeks with FU at 2 and 4 months
Secondary Outcome Measures
NameTimeMethod
Brain activity during functional brain imaging2 weeks

Trial Locations

Locations (1)

University of Kansas Medical Center

🇺🇸

Kansas City, Kansas, United States

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