The National Institute of Neurological Disorders and Stroke, part of the National Institutes of Health, is looking for individuals to participate in clinical studies. Participating in clinical trials allows you to play an active role in research on the nature and causes of many disorders of the brain and nervous system, and to possibly help physician-scientists develop future treatments. The information below is designed to help you quickly learn about actively recruiting research studies for which you or someone you know may be eligible.

Description:

Objective: The goals of this study are to 1. replicate the finding that exercise after exposure to images enhances their subsequent recall, 2. extend the question to words and logical rules, 3. examine the mechanism of the effect using exercise biomarkers and fMRI and 4. explore its usefulness as an aid to memory in individuals with traumatic brain injury (TBI). 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.

Eligibility Criteria:

- INCLUSION CRITERIA: - Age 18-45 (inclusive) - English speaking and writing - For TBI patients: - 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: - Inability to give informed consent - 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

Study Design:

Study Location:

Maryland