Cognitive Deterioration Clinical Trial
Official title:
Exercise, Age-Related Memory Decline, And Hippocampal Function
Verified date | March 2020 |
Source | New York State Psychiatric Institute |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to test the hypothesis that aerobic exercise leads increased cerebral blood volume in the dentate gyrus of the hippocampus in a sample of young and older adults.
Status | Completed |
Enrollment | 233 |
Est. completion date | December 31, 2019 |
Est. primary completion date | December 31, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 20 Years to 75 Years |
Eligibility |
Inclusion Criteria: 1. Age 20-75 years 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: 1. Ischemic changes or abnormal resting cardiogram, abnormal blood pressure responses, or an significant ectopy during aerobic capacity testing 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 21. MRI Exclusion Criteria: Cardiac Pacemaker; Internal Pump; Insulin Pump; Tattoo; eyeliner; Wire Sutures; Internal Metal Objects; Metal Slivers in Eye; Prosthesis; Hearing Aid Implants; Neurostimulator; Metal Fragments; Brain Aneurysm Clips; Vascular Clips; Breast Expander; Vena Cava Filter; Heart Valve; Metal Stents; Asthma; Hay-Fever; Sickle Cell Disease; Kidney Disease; Machinist or ever worked with heavy metals Interview; Contraindication to gadolinium, including prior adverse reaction to gadolinium, past or current history of severe breathing difficulty that has been treated by a physician (e.g., asthma, COPD, etc.), and sickle cell disease. History of renal impairment or estimated glomerular filtration rate <30 L/min/1.73m2 is also exclusionary; Machinist or ever worked with heavy metals Interview; Have had more than one MRI scans with Gadolinium |
Country | Name | City | State |
---|---|---|---|
United States | Columbia University Medical Center | New York | New York |
Lead Sponsor | Collaborator |
---|---|
New York State Psychiatric Institute |
United States,
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. Epub 2007 — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | dentate gyrus cerebral blood volume | change from before (pre) to after (post) 12 weeks of training | ||
Secondary | cognitive function | measures of memory, executive function, attention/processing speed, language, and general intelligence | change from before (pre) to after (post) 12 weeks of training | |
Secondary | aerobic capacity | change from before (pre) to after (post) 12 weeks of training | ||
Secondary | cerebral blood flow | arterial spin labeling fMRI | change from before (pre) to after (post) 12 weeks of training |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04138446 -
Effects of Acute Hypobaric Hypoxia Exposure on Neurocognitive Performance of Pre-hospital Emergency Service Providers
|
N/A | |
Recruiting |
NCT05497427 -
Normative Database and Test-Retest Reliability for BrainCheck Assessments
|
||
Not yet recruiting |
NCT06380998 -
Effects of Petroleum Compounds on Psychological Health and Cognitive Functions
|
||
Recruiting |
NCT06056934 -
Pain Management in Elderly Patients With or Without Cognitive Frailty Hospitalized "ALGOGER"
|
||
Recruiting |
NCT04263194 -
Network-based rTMS in Alzheimer's Disease
|
N/A | |
Completed |
NCT02288221 -
Safe & Easy Environment at Home for Patients Presenting a Frail Syndrome
|
N/A | |
Completed |
NCT02518243 -
Safe & Easy for Alzheimer's Disease and Related Pathologies
|
N/A | |
Recruiting |
NCT05728801 -
Decoding the Cognitive Trajectory of Hong Kong SuperAgers: a Longitudinal Follow-up Study
|
||
Terminated |
NCT03032471 -
Swiss SOS MoCA - DCI Study
|
||
Completed |
NCT05863065 -
Personalized Virtual Reality Naturalistic Scenarios in Cognitive Impairment
|
N/A | |
Recruiting |
NCT03657745 -
Alzheimer's Disease Treatment With Combination of 40Hz Light and Cognitive Therapy
|
||
Terminated |
NCT03353987 -
Preoperative Cognitive Training for Postoperative Cognitive Dysfunction
|
N/A | |
Completed |
NCT03246269 -
Normative Values for the German Version of the Montreal Cognitive Assessment (MoCA)
|
||
Completed |
NCT02968992 -
Effects of rhLactoferrin on Chronic Inflammation in the Elderly
|
Phase 2 | |
Not yet recruiting |
NCT06256666 -
Objective Measurement of Pain in Individuals With Cognitive Deterioration Utilizing Electroencephalography
|
||
Active, not recruiting |
NCT05818423 -
Brain Health Together: A Live-Streaming Group-Based Digital Program
|
N/A |