Effects of Exercise on Memory in Healthy and Brain-Injured Individuals
NCT ID: NCT01939769
Last Updated: 2017-08-30
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
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
TERMINATED
PHASE1
42 participants
INTERVENTIONAL
2013-08-31
2017-08-28
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
\- Research has shown that one exercise session may improve a person s ability to recall information they learned before the exercise. Knowing how exercise changes brain activity to improve memory can help researchers understand how memory works and how to improve it in people with memory problems. This study compares two kinds of exercise on a stationary bike for their ability to temporarily improve memory on certain tests. Researchers will look at the effect of exercise on body chemistry by drawing blood and collecting saliva.
Objectives:
\- To understand how a single session of exercise affects memory testing in healthy people and people who have had traumatic brain injury (TBI).
Eligibility:
* Adults ages 18 through 45 with TBI.
* Healthy adult volunteers, ages 18 through 45.
Design:
* Participants will be screened with medical history and physical exam. This will take about 1 hour.
* Participants with TBI will also be screened with a test of their memory. This will take another hour.
* Visit 1 will take about 3 hours. Participants will:
\<TAB\>- Have a tube inserted in their arm for drawing blood during the tests.
\<TAB\>- Take memory tests. They will look at pictures, symbols, and words, then answer questions.
\<TAB\>- Give a saliva sample by chewing on a small sponge for 2 minutes.
\<TAB\>- Exercise on a stationary bike.
\<TAB\>- Take the memory tests again.
\- Visit 2 will take place 1 week later. Participants will take the memory tests only.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Aerobic Exercise to Improve Memory in TBI
NCT01952704
Influence of Physical Exercise on Cognitive Functioning of Traumatic Brain Injury Patients
NCT01395472
Effects of Aerobic Exercise on Cognition, Mood and Fatigue Following TBI
NCT00619463
Effects of Mental Stimulation in Patients With Mild Cognitive Impairment
NCT01212692
Effect of Acute Physical Exercise on Memory
NCT04680494
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Study population: Healthy adult volunteers and individuals with TBI.
Design: The main, clinical, experiment has a parallel, repeated-measures design, where four groups (two each of healthy subjects and participants with TBI) will encode pictures, words and rules and then exercise at either a high or very low (placebo) intensity. Recall will be tested one hour and again at seven days after exercise. Blood and saliva will be collected before and immediately after exercise and assayed for biomarkers of exercise, thought to be possible mediators of the memory effect. In a parallel-design fMRI experiment, intended to explore the brain basis of the effect of exercise on memory, healthy volunteers will view pictures, exercise at a high or low intensity, and then perform a recall task in the scanner. The analysis will look for differences in location and extent of evoked brain activations evoked by picture recall after low and high intensity exercise.
Outcome measures: The primary outcome measure is recall of visual material one hour after exercise. Secondary measures will be the recall of word lists and letter/digit symbol matching (logical memory) and activations on fMRI. The blood and saliva biomarkers will are included as exploratory outcomes.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Exercise - Low-intensity exercise
Exercise - High-intensity exercise
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Age 18-45 (inclusive)
* English speaking and writing
* For TBI patients:\<TAB\>
* History of TBI (defined according to the American Congress of Rehabilitation Medicine Criteria: History of having sustained a traumatically induced physiological disruption of brain function at least 2 months before participation)
* Evidence of at least moderate TBI severity. Evidence for intensity of TBI will be any one of the following 3 criteria:
1. GCS greater than or equal to 9 (obtained in Emergency Room and noted in medical record)
2. Post-traumatic amnesia \> 24 hours
3. TBI-related abnormality on neuroimaging (either CT or MRI)
* Documented memory deficit, i.e., a score of 1 standard deviation or more below age-adjusted norm on a recognized clinical test of memory, such as the Wexler Memory Scale, within the last two years.
* Enrollment in Protocol 11-N-0084
* Right-handedness for fMRI participants
Exclusion Criteria
* History of major neurological or psychiatric illness, e.g., neurodegenerative disorder, stroke, congenital or genetic disorder, currently symptomatic major depressive disorder, schizophrenia
* History of exercise intolerance
* Any finding on examination indicative of cardiac or respiratory compromise
* History of heart disease
* History of pulmonary disease, other than controlled, non-exercise-induced asthma
* History of uncontrolled diabetes
* Resting heart rate \> 100 BPM
* Resting systolic blood pressure \> 140 mmHg or diastolic blood pressure \> 100 mmHg
* Peripheral condition making completion of the exercise protocol impossible, such as severe osteoarthritis or chronic pain
* Pregnancy
* For healthy subjects undergoing MRI:
* Ferromagnetic metal in the cranial cavity or eye, e.g. aneurysm clip, implanted neural stimulator, cochlear implant, or ocular foreign body
* Implanted cardiac pacemaker or auto-defibrillator or pump
* Non-removable body piercing
* Claustrophobia
* Inability to lie supine for two hours
* Any structural brain abnormality, such as tumor or stroke
18 Years
45 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
National Institute of Neurological Disorders and Stroke (NINDS)
NIH
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Eric M Wassermann, M.D.
Role: PRINCIPAL_INVESTIGATOR
National Institute of Neurological Disorders and Stroke (NINDS)
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
National Institutes of Health Clinical Center, 9000 Rockville Pike
Bethesda, Maryland, United States
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Ahlskog JE, Geda YE, Graff-Radford NR, Petersen RC. Physical exercise as a preventive or disease-modifying treatment of dementia and brain aging. Mayo Clin Proc. 2011 Sep;86(9):876-84. doi: 10.4065/mcp.2011.0252.
Craig CL, Marshall AL, Sjostrom M, Bauman AE, Booth ML, Ainsworth BE, Pratt M, Ekelund U, Yngve A, Sallis JF, Oja P. International physical activity questionnaire: 12-country reliability and validity. Med Sci Sports Exerc. 2003 Aug;35(8):1381-95. doi: 10.1249/01.MSS.0000078924.61453.FB.
Borg G. Perceived exertion as an indicator of somatic stress. Scand J Rehabil Med. 1970;2(2):92-8. No abstract available.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
13-N-0198
Identifier Type: -
Identifier Source: secondary_id
130198
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.