Effects of Exercise on Memory in Healthy and Brain-Injured Individuals

This study is currently recruiting participants.
Verified August 2013 by National Institutes of Health Clinical Center (CC)
Sponsor:
Information provided by (Responsible Party):
National Institutes of Health Clinical Center (CC) ( National Institute of Neurological Disorders and Stroke (NINDS) )
ClinicalTrials.gov Identifier:
NCT01939769
First received: September 6, 2013
Last updated: March 14, 2014
Last verified: August 2013

September 6, 2013
March 14, 2014
August 2013
March 2015   (final data collection date for primary outcome measure)
Recall of pictures [ Time Frame: 2 years ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01939769 on ClinicalTrials.gov Archive Site
  • Recall of word lists [ Time Frame: 2 years ] [ Designated as safety issue: No ]
  • Digit-symbol substitution performance [ Time Frame: 2 years ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Effects of Exercise on Memory in Healthy and Brain-Injured Individuals
Acute Effects of Exercise on Memory in Healthy and Brain-Injured Individuals

Background:

- 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.

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.

Interventional
Phase 1
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind
Primary Purpose: Treatment
Traumatic Brain Injury
  • Other: Exercise - Low-intensity exercise
    N/A
  • Other: Exercise - High-intensity exercise
    N/A
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
105
March 2015
March 2015   (final data collection date for primary outcome measure)
  • INCLUSION CRITERIA:

< TAB>

  • 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:

  • 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
Both
18 Years to 45 Years
Yes
Contact: Michael C Tierney (301) 496-0221 tierneym@ninds.nih.gov
United States
 
NCT01939769
130198, 13-N-0198
Not Provided
National Institutes of Health Clinical Center (CC) ( National Institute of Neurological Disorders and Stroke (NINDS) )
National Institute of Neurological Disorders and Stroke (NINDS)
Not Provided
Principal Investigator: Eric M Wassermann, M.D. National Institute of Neurological Disorders and Stroke (NINDS)
National Institutes of Health Clinical Center (CC)
August 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP