Memory Impairment Clinical Trial
— METOfficial title:
Simultaneous Aerobic Exercise and Memory Training in Older Adults With Subjective Memory Complaints
NCT number | NCT02433691 |
Other study ID # | 14-001411 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | January 2015 |
Est. completion date | June 2017 |
Verified date | April 2018 |
Source | University of California, Los Angeles |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This pilot study is a first step in a rapidly growing area of clinical research to create the most effective means to combat age-related losses in cognitive function through preventive lifestyle strategies such as physical exercise and memory training. This study will develop innovative simultaneous exercise and memory training programs in non-demented volunteers with subjective memory complaints (controls or MCI). Our primary goal is to assess the cognitive impact of 4-week memory training programs done twice weekly: 1. during simultaneous aerobic exercise (SIM-AR-MET), 2. sequentially after aerobic exercise (SEQ-AR-MET), or 3. without aerobic exercise (replaced with sequential stretching and toning) (SEQ-ST-MET). The investigators will also measure potential metabolic (e.g., glucose, lipid panel) and molecular (serum BDNF) mediators of observed cognitive changes in a subset of participants (those at the UCLA CTRC/IPCN site).
Status | Completed |
Enrollment | 60 |
Est. completion date | June 2017 |
Est. primary completion date | June 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 60 Years to 75 Years |
Eligibility |
Inclusion Criteria: - In good health - Have memory problems or complaints - Living independently Exclusion Criteria: - History of neurodegenerative disease or dementia - Major psychiatric conditions - Neurological disorders - Active alcohol or substance abuse - Head trauma or systemic diseases affecting brain function - Uncontrolled hypertension or cardiovascular disease |
Country | Name | City | State |
---|---|---|---|
United States | UCLA Longevity Center | Los Angeles | California |
Lead Sponsor | Collaborator |
---|---|
David Merrill, MD, PhD |
United States,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Effects of the MET interventions on cognition (comparing baseline vs. end-of-study NP testing) | Change from baseline in composite measure of memory related tasks including retention, attention, and mood. | up to 9 months | |
Secondary | Changes in BDNF levels in response to the interventions | Increase of baseline measurement for BDNF levels. | up to 9 months | |
Secondary | Physical health measures | Change in baseline in composite measurement of weight (loss), and increase in physical activity. | up to 9 months |
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