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CompletedNCT03016702CogResUpdated Aug 14, 2017

The Cognitive Resilience Study

An interventional study of Cognitive stress tests during functional MRI and Cognitive stress tests during gait task in Alzheimer Disease, sponsored by Duke University. Completed at 1 site in United States. Open to participants aged 58 Years to 70 Years. Per ClinicalTrials.gov, last updated 2017-08-14.

Sponsored by Duke University · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
29
Allocation
Non-randomized
Ages
58 Years to 70 Years
Sex
All
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Study summary

The purpose of this study is to test whether two new cognitive "stress tests" may help distinguish between people at lower or higher genetic risk of Alzheimer's Disease. The investigators are trying to understand how these cognitive "stress tests" work in people who have not been diagnosed with Alzheimer's Disease and are not exhibiting symptoms of Alzheimer's Disease. Study subjects will undergo testing of memory and executive function during functional magnetic resonance image (fMRI) of the brain and also during a walking test.

Read the detailed description

The objective is to establish the feasibility and evaluate the role of two novel tests of cognitive resilience for use in identification of early Alzheimer's Disease. The investigators hypothesize that exposure to the controlled stressor of increased cognitive task demand will evoke measurable phenotypes of poor resilience, which will be associated with Alzheimer's Disease risk. The study will include 30 volunteer participants from the Duke Alzheimer's Disease Prevention Registry (ADPR). The ADPR cohort has been characterized according to genetic risk based on genotype at loci associated with Alzheimer's Disease. The investigators will recruit a sample from the ADPR that includes 15 people in the "genetic high risk" group and 15 people, matched by age, in the "genetic low risk" group. Investigators and experimenters are masked to the genetic profile of all participants. All participants will undergo two cognitive stress test protocols. Both protocols include memory and executive function components, one done during functional MRI and one while ambulating on a force sensor mat. Both cognitive stress tests are minimal risk; the primary risk of this study is loss of confidentiality. Genetic testing is not performed as part of this protocol; the sampling strategy will make use of prior genetic testing results, which are not revealed to the primary investigators. In addition to determining whether scores on the two novel tests statistically differ by AD risk groups, the project will establish the tests' feasibility and characteristics for use in future study.

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Conditions studied

  • Alzheimer Disease

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03

In context

Alzheimer Disease

3,678 studies on the registry are indexed under Alzheimer Disease; 872 are open to participants now.

This study's enrollment of 29 is below the median of 70 across 2,808 interventional studies indexed under Alzheimer Disease.

Browse Alzheimer Disease studies →

Lead sponsor

Duke University is the lead sponsor of 2,025 studies on the registry; 275 are open to participants now.

Of its 194 completed or terminated interventional studies of FDA-regulated products, 159 (82%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
58 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Able to walk 2 minutes without assistive device or assistance from another person
  • Cognitive function within normal limits

Exclusion criteria

Exclusion Criteria:

  • Unable to undergo MRI
  • Left handed
  • Red/Green Color Blind
  • Severe vision impairments
  • Diagnosis of Alzheimer's Disease or other dementia/memory problem
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Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
29 participants (actual)

Study arms

  • Experimental
    High Risk Alzheimer's Disease

    This group includes subjects with APOEe4 homozygotes, the genetic profile associated with the highest risk for late-onset AD and the next highest-risk group, APOE e3/e4 heterozygotes. To target the highest risk among the APOEe3/e4 heterozygotes in ADPR, the study team will consider TOMM40-'523 variant status. Although there is uncertainty about the independent role of TOMM40 in AD risk-stratification (especially across racial/ethnic groups), this study will use TOMM40-'523 to guide heterozygote selection based on findings that among e3/e4 heterozygotes, longer TOMM40-523 polyT sequences are associated with earlier age of onset for late-onset AD.

    Other: Cognitive stress tests during functional MRI · Other: Cognitive stress tests during gait task

  • Experimental
    Low Risk Alzheimer Disease

    This group includes e2/e2 homozygotes (rare) and e2/e3 heterozygotes. the genetic profile associated with low risk for late-onset development of Alzheimer's disease.

    Other: Cognitive stress tests during functional MRI · Other: Cognitive stress tests during gait task

Interventions

  • OtherCognitive stress tests during functional MRI

    Subjects will undergo progressively more complex cognitive stress tests that assess memory and executive function while undergoing fMRI.

  • OtherCognitive stress tests during gait task

    Subjects will undergo progressively more complex cognitive stress tests that assess memory and executive function both in sitting and while ambulating on a force sensor mat.

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What researchers measure

Primary outcomes

  1. Change in reaction time during memory testing during fMRI

    The primary dependent variable will be change in reaction time when comparing a neutral memory task to a stress condition. Reaction time will be in ms and will be recorded while the subject is undergoing fMRI.

    Time frame: Measured immediately during one hour fMRI

  2. Change in reaction time during executive function testing during fMRI

    The primary dependent variable will be change in reaction time when comparing a neutral executive function task to a stress condition. Reaction time will be in ms and will be recorded while the subject is undergoing fMRI.

    Time frame: Measured immediately during one hour fMRI

  3. Change in accuracy during memory testing during gait task

    The primary dependent variable will be DTEcog = (Dual task \[cognitive score\] - Single Task \[cognitive score\] / Single task \[cognitive score\]. For the memory task, the primary cognitive measure will be the number of correct responses.

    Time frame: Measured immediately during one hour gait session

  4. Change in reaction time during executive function testing during gait task

    The primary dependent variable will be DTEcog = (Dual task \[cognitive score\] - Single Task \[cognitive score\] / Single task \[cognitive score\]. For the executive task, the primary cognitive measure in the DTEcog calculation will be reaction time.

    Time frame: Measured immediately during one hour gait session

Secondary outcomes

  1. Change in accuracy during memory testing during fMRI

    Secondary dependent variables are accuracy (% correct) when comparing a neutral memory task to a stress condition.

    Time frame: Measured immediately during one hour fMRI

  2. Change in accuracy during executive function testing during fMRI

    Secondary dependent variables are accuracy (% correct) when comparing a neutral memory task to a stress condition.

    Time frame: Measured immediately during one hour fMRI

  3. Brain activation during memory testing during fMRI

    Group differences in brain activation provoked by the memory stress condition will be assessed using brain maps that compare block-average BOLD signal for resting vs neutral task, resting vs stress task, neutral vs stress task.

    Time frame: Measured immediately during one hour fMRI

  4. Brain activation during executive function testing during fMRI

    Group differences in brain activation provoked by the executive function stress condition will be assessed using brain maps that compare block-average BOLD signal for resting vs neutral task, resting vs stress task, neutral vs stress task.

    Time frame: Measured immediately during one hour fMRI

  5. Change in gait performance provoked by memory dual tasking

    The secondary dependent variable will be DTEmob = (Dual task\[mobility score\] - Single Task\[mobility score\] / Single task \[mobility score\]. For both memory and executive tasks, the mobility measure in the DTEmob calculation will be gait speed.

    Time frame: Measured immediately during one hour gait session

  6. Change in gait performance provoked by executive function dual tasking

    The secondary dependent variable will be DTEmob = (Dual task\[mobility score\] - Single Task\[mobility score\] / Single task \[mobility score\]. For both memory and executive tasks, the mobility measure in the DTEmob calculation will be gait speed.

    Time frame: Measured immediately during one hour gait session

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Study locations

1 site
  • Duke University Medical Center
    Durham, North Carolina 27710, United States
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 14, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03016702
Lead sponsor
Duke University
Collaborators
National Institute on Aging (NIA), Bryan Alzheimer's Disease Research Center, Duke University Center for the Study of Aging and Human Development
Responsible party
Sponsor
First posted
Jan 10, 2017
Start date
Feb 27, 2017
Primary completion
Aug 9, 2017
Completion
Aug 9, 2017
Last update
Aug 14, 2017

Study contacts

Heather Whitson, MD, MHS
principal investigator · Duke University Aging Center

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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