Exercise, Age-Related Memory Decline, And Hippocampal Function
NCT ID: NCT01329653
Last Updated: 2020-03-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
233 participants
INTERVENTIONAL
2011-06-30
2019-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
BASIC_SCIENCE
SINGLE
Study Groups
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aerobic training
12 weeks of aerobic training, 4X/week
aerobic training
12 weeks of aerobic training, 4X/week
wait list control
wait list control condition, 12 weeks to parallel the active intervention group
Wait list
wait list control condition
Interventions
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aerobic training
12 weeks of aerobic training, 4X/week
Wait list
wait list control condition
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. English-speaking
3. Ambulatory
4. "Average" fitness as determined by ACSM's Guidelines for Exercise Testing and Prescription (for men, VO2max \< 43 for age 20-39 years, \< 38 for age 40-49 years, \< 35 for age 50-59, \< 31 for age 60-75; for women, \< 36 for age \< 30 years, \< 34 for age 30-39 years, \< 32 for age 40-49 years, \<25 for age 50-59 years, \< 24 for age 60-75 years
5. BMI \<35
Exclusion Criteria
2. Cardiovascular disease
3. BMI \> 35
4. Uncontrolled high blood pressure (systolic blood pressure ≥ 140 mmHg; or diastolic blood pressure ≥ 90mmHg on two measures)
5. Any condition for which aerobic training is counter-indicated, including persons with evidence or history of medical or orthopedic conditions which might make participation problematic.
6. Current or recent (evidence of disease x 5 years) non-skin neoplastic disease or melanoma. Prostatic carcinoma will not be grounds for exclusion.
7. Active hepatic disease (not a history of hepatitis) or primary renal disease requiring dialysis, primary untreated endocrine diseases, e.g., Cushing's disease or primary hypothalamic failure or insulin dependent diabetes (Type I or II). Welltreated hypothyroidism will not be excluded.
8. History of chemotherapy
9. HIV infection
10. Pregnant or lactating (participation allowed 3 months after ceasing lactation).
11. Medications that alter inflammation or autonomic nervous system activity
12. Any history of psychosis or ECT
13. Current or recent (past one year) Major Depressive Disorder, Bipolar Disorder
14. Current or recent (within past 12 months) alcohol or substance abuse or dependence. Recent use (past month) of recreational drugs.
15. Dementia Rating Scale (DRS) score less than 135. Medical History Interview
16. Neurological Disorders Dementia Rating Scale
17. Stroke Telephone screen
18. Alzheimer's Disease Telephone screen
19. Smoking Telephone screen
20. Prior participation in another Dr. Sloan Exercise Study
20 Years
75 Years
ALL
Yes
Sponsors
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New York State Psychiatric Institute
OTHER
Responsible Party
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Richard Sloan
Research Scientist
Principal Investigators
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Richard P Sloan, PhD
Role: PRINCIPAL_INVESTIGATOR
Columbia University
Locations
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Columbia University Medical Center
New York, New York, United States
Countries
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References
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Pereira AC, Huddleston DE, Brickman AM, Sosunov AA, Hen R, McKhann GM, Sloan R, Gage FH, Brown TR, Small SA. An in vivo correlate of exercise-induced neurogenesis in the adult dentate gyrus. Proc Natl Acad Sci U S A. 2007 Mar 27;104(13):5638-43. doi: 10.1073/pnas.0611721104. Epub 2007 Mar 20.
Other Identifiers
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AG035015
Identifier Type: OTHER
Identifier Source: secondary_id
#6219/#7161R
Identifier Type: -
Identifier Source: org_study_id
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