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.

Study Overview

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.

Study Type

Interventional

Enrollment (Actual)

42

Phase

  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Maryland
      • Bethesda, Maryland, United States, 20892
        • National Institutes of Health Clinical Center, 9000 Rockville Pike

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 45 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

  • 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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Recall of pictures
Time Frame: 2 years
2 years

Secondary Outcome Measures

Outcome Measure
Time Frame
Recall of word lists
Time Frame: 2 years
2 years
Digit-symbol substitution performance
Time Frame: 2 years
2 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

August 31, 2013

Primary Completion (ACTUAL)

May 21, 2015

Study Completion (ACTUAL)

August 28, 2017

Study Registration Dates

First Submitted

September 6, 2013

First Submitted That Met QC Criteria

September 6, 2013

First Posted (ESTIMATE)

September 11, 2013

Study Record Updates

Last Update Posted (ACTUAL)

August 30, 2017

Last Update Submitted That Met QC Criteria

August 29, 2017

Last Verified

August 28, 2017

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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