Now Available for Public Comment: Notice of Proposed Rulemaking (NPRM) for FDAAA 801 and NIH Draft Reporting Policy for NIH-Funded Trials

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

This study is currently recruiting participants. (see Contacts and Locations)
Verified June 2014 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: November 4, 2014
Last verified: June 2014
  Purpose

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.


Condition Intervention Phase
Traumatic Brain Injury
Other: Exercise - Low-intensity exercise
Other: Exercise - High-intensity exercise
Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind
Primary Purpose: Treatment
Official Title: Acute Effects of Exercise on Memory in Healthy and Brain-Injured Individuals

Resource links provided by NLM:


Further study details as provided by National Institutes of Health Clinical Center (CC):

Primary Outcome Measures:
  • Recall of pictures [ Time Frame: 2 years ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • 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 ]

Estimated Enrollment: 105
Study Start Date: August 2013
Estimated Study Completion Date: November 2014
Primary Completion Date: November 2014 (Final data collection date for primary outcome measure)
Intervention Details:
    Other: Exercise - Low-intensity exercise
    N/A
    Other: Exercise - High-intensity exercise
    N/A
Detailed 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

Ages Eligible for Study:   18 Years to 45 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria
  • 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
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01939769

Contacts
Contact: Michael C Tierney (301) 496-0221 tierneym@ninds.nih.gov

Locations
United States, Maryland
National Institutes of Health Clinical Center, 9000 Rockville Pike Recruiting
Bethesda, Maryland, United States, 20892
Contact: For more information at the NIH Clinical Center contact Patient Recruitment and Public Liaison Office (PRPL)    800-411-1222 ext TTY8664111010    prpl@mail.cc.nih.gov   
Sponsors and Collaborators
Investigators
Principal Investigator: Eric M Wassermann, M.D. National Institute of Neurological Disorders and Stroke (NINDS)
  More Information

Additional Information:
Publications:
Responsible Party: National Institutes of Health Clinical Center (CC) ( National Institute of Neurological Disorders and Stroke (NINDS) )
ClinicalTrials.gov Identifier: NCT01939769     History of Changes
Other Study ID Numbers: 130198, 13-N-0198
Study First Received: September 6, 2013
Last Updated: November 4, 2014
Health Authority: United States: Federal Government

Keywords provided by National Institutes of Health Clinical Center (CC):
fMRI
Catecholamines
Stress
Exercise
Memory

Additional relevant MeSH terms:
Brain Injuries
Brain Diseases
Central Nervous System Diseases
Craniocerebral Trauma
Nervous System Diseases
Trauma, Nervous System
Wounds and Injuries

ClinicalTrials.gov processed this record on November 27, 2014