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Clinical Trials/NCT01180127
NCT01180127CompletedNot Applicable

Study of the Impact of a Flavanol Containing Food Product and Exercise on Cognitive Function and Brain Structure

New York State Psychiatric Institute0 sites41 target enrollmentStarted: December 1, 2009Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
41
Primary Endpoint
ModBent (Modified Benton Visual Retention Test)

Study Overview

Brief Summary

This is a randomized controlled trial to test the impact of a flavonol containing food product and aerobic exercise on cognitive function and brain structure.

Detailed Description

I. Background and Significance A. The epidemiology of cognitive aging. Encompassing multiple cognitive domains, higher order thinking includes memory, language, abstract reasoning, and visuospatial ability. A range of studies have established that memory is a cognitive domain differentially targeted by the normal aging process. With an increase in lifespan and a decrease in co-morbid diseases, aging individuals expect to lead cognitively-challenging lives. Even mild forgetfulness, therefore, is no longer considered 'benign'. Indeed, with the exponential growth of the aging population, and since memory decline will occur in all of us as we age, age-related memory decline has emerged as a major societal problem.

B. The anatomy of cognitive aging. A range of studies in humans, non-human primates and rodents have established that the hippocampal formation, a brain circuit vital for memory, is targeted by the aging process. Age-related hippocampal dysfunction is therefore a major contributor to age-related memory decline.

The hippocampal formation is organized as a circuit, made up of separate but interconnected regions, including the entorhinal cortex, the dentate gyrus, the CA subfields, and the subiculum. Because of hippocampal circuit properties, dysfunction in one subregion will affect the function of neighboring subregions and the hippocampal circuit as a whole. Thus, when confronted with any process that causes the hippocampal circuit to malfunction, pinpointing the subregion that is most effected becomes an important goal.

In the case of age-related memory decline, a range of studies in humans, non-human primates, and rodents, have suggested that normal aging causes hippocampal dysfunction by differentially targeting the dentate gyrus.

C. Imaging cognitive aging. The anatomical organization of the hippocampal circuit and the differential vulnerability of the dentate gyrus to cognitive aging imposes specific requirements on brain imaging techniques. Specifically, an imaging technique must be able to assess the functional integrity of the multiple hippocampal subregions, in particular the dentate gyrus. With this in mind, our lab has been dedicated to optimizing a functional brain imaging approach applicable to both the human and rodent hippocampal formation. We have recently achieved this goal, and have been applying our cross-species imaging capabilities to investigate a range of process that affect hippocampal function.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Factorial
Primary Purpose
Basic Science
Masking
Single (Investigator)

Eligibility Criteria

Ages
50 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •English-speaking
  • •Post-menopausal (women only), no estrogen replacement therapy
  • •VO2max < 36 and 33 ml/kg/min for men age 50-59 and 60-69 respectively; < 29 and 27 ml/kg/min for women age 50-59 and 60-75 respectively.
  • •Baecke Physical Activity Sports Score ≤ 2
  • •Medical clearance to participate in the study (normal serum electrolyte, BUN, creatinine levels, normal blood pressure and resting cardiogram)

Exclusion Criteria

  • •Use of psychotropic medications
  • •Current psychiatric disorder
  • •Any condition for which aerobic training is counter-indicated
  • •Habitual consumers of dietary or herbal supplements, including Gingko, flavonoid, and dietary herbal or plant extracts
  • •Lactose Intolerance
  • •Individuals who report directly to any of the study investigators
  • •Exclusion Criteria (MRI-related)
  • •Cardiac Pacemaker
  • •Internal Pump
  • •Insulin Pump
  • •Tattoo eyeliner
  • •Wire Sutures
  • •Internal Metal Objects
  • •Metal Slivers in Eye
  • •Hearing Aid Implants
  • •Neurostimulator
  • •Metal Fragments
  • •Brain Aneurysm Clips
  • •Vascular Clips
  • •Breast Expander
  • •Vena Cava Filter
  • •Heart Valve
  • •Metal Stents
  • •Sickle Cell Disease
  • •Kidney Disease

Arms & Interventions

exercise, dietary intervention

Active Comparator

aerobic training and flavanol containing food product for 12 weeks

Intervention: Flavanol containing food product (Dietary Supplement)

exercise, dietary intervention

Active Comparator

aerobic training and flavanol containing food product for 12 weeks

Intervention: Aerobic training (Behavioral)

no exercise, dietary intervention

Active Comparator

wait list control plus flavanol containing food product for 12 weeks

Intervention: Flavanol containing food product (Dietary Supplement)

no exercise, dietary intervention

Active Comparator

wait list control plus flavanol containing food product for 12 weeks

Intervention: Wait list control (Behavioral)

exercise, food product lacking flavanol

Active Comparator

aerobic training plus food product without flavanol for 12 weeks

Intervention: Aerobic training (Behavioral)

exercise, food product lacking flavanol

Active Comparator

aerobic training plus food product without flavanol for 12 weeks

Intervention: Food product lacking flavanol (Dietary Supplement)

wait list control food additive without flavanol

Placebo Comparator

wait list control plus food product without flavanol for 12 weeks

Intervention: Food product lacking flavanol (Dietary Supplement)

wait list control food additive without flavanol

Placebo Comparator

wait list control plus food product without flavanol for 12 weeks

Intervention: Wait list control (Behavioral)

Outcomes

Primary Outcomes

ModBent (Modified Benton Visual Retention Test)

Time Frame: Up to 12 weeks after exercise/dietary intervention exposure

This is an object recognition task. Participants view a complex stimulus, then are asked to select which one of two objects was identical to the studied stimulus. After a series of these matching trials, during the subsequent recognition trials participants are shown serially individual complex objects and asked to indicate whether the object was identical to any of the target stimuli viewed during the matching trials. Their reaction time for correct responses, measured in milliseconds, is the unit of measurement.

CBV-fMRI (Cerebral Blood Volume-functional Magnetic Resonance Imaging)

Time Frame: Up to 12 weeks after exercise/dietary intervention exposure

In steady state conditions, CBV is an indirect measure of basal metabolism in the brain. CBV-fMRI is a technique that generates maps of basal metabolism across different brain regions

Secondary Outcomes

  • VO2max(Up to 12 weeks after exercise/dietary intervention exposure)
  • Modified Rey Auditory Verbal Learning Test(Up to 12 weeks after exercise/dietary intervention exposure)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Richard Sloan

Research Scientist

New York State Psychiatric Institute

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