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Clinical Trials/NCT00643266
NCT00643266
Completed
Not Applicable

Memory Interventions for Older Adults

Baycrest1 site in 1 country91 target enrollmentFebruary 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Amnestic Mild Cognitive Impairment
Sponsor
Baycrest
Enrollment
91
Locations
1
Primary Endpoint
Recollection estimates
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

We have developed a training intervention that successfully improves older adults' memory. We have also shown that older adults whose memory is as good as younger adults' memory (Hi-Old) use an altered pattern of memory-related brain activity compared to younger adults, whereas healthy older adults with poorer memory (Lo-Old) do not. We have also shown that individuals with amnestic Mild Cognitive Impairment (aMCI) have impairments of conscious, effortful, Recollection-based memory processes, whereas their automatic, Familiarity-based memory processes are intact. Our primary current goal is to investigate whether our successful memory intervention will improve Recollection and produce induce altered patterns of brain activity in the Lo-Old and aMCI.

Young, Lo-Old, Hi-Old, and aMCI will be scanned using functional magnetic resonance imaging while performing two memory tasks. Half of the Lo-Old and half of the aMCI will then receive the memory intervention, while the other half in each group will receive a control program consisting of information and games about aging. The Lo-Old and aMCI will then be rescanned while performing the two memory tasks. We predict that the memory intervention will improve performance on a number of memory tasks, and will induce altered patterns of brain activity. In the Lo-Old, their brain activity after the memory intervention will look more like the Hi-Old, while brain activity will become more focal in the aMCI.

Registry
clinicaltrials.gov
Start Date
February 2008
End Date
August 2013
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Baycrest
Responsible Party
Principal Investigator
Principal Investigator

Dr. Nicole D. Anderson

Senior Scientist

Baycrest

Eligibility Criteria

Inclusion Criteria

  • 65-90 years old
  • English as a first language or learned before kindergarten
  • Right handed

Exclusion Criteria

  • Neurologic disorder
  • Major medical disorder affecting cognition
  • Psychiatric disorder
  • Metal in the body that poses a hazard in the MRI scanner

Outcomes

Primary Outcomes

Recollection estimates

Time Frame: Immediately post-training and three months post-training

Recollection, defined as Correct "yes" responses to "Same" repetitions minus Incorrect "yes" responses to "Different" repetitions, as a function of condition (trained versus control), lag (3, 16) and time (pre-, post-, and 3 month follow-up)

Secondary Outcomes

  • Transfer to other recollection-dependent task and to subjective memory measures(Immediately post-training and three months post-training)
  • Brain activation as assessed by functional magnetic resonance imaging(Immediately post-training)

Study Sites (1)

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