Effect of Exercise Training on Physical, Cognitive, and Behavioral Function in People With TBI
Primary Purpose
Traumatic Brain Injury
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Exercise
Sponsored by
About this trial
This is an interventional basic science trial for Traumatic Brain Injury focused on measuring Aerobic Exercise Training, Balance, TBI
Eligibility Criteria
INCLUSION CRITERIA:
- Ages 18 to 79 inclusive
- Diagnosis of non-penetrating TBI
- Injury occurred at least 12 months prior to enrollment
- Physically inactive as identified by a physician
- Able to stand and walk independently and safely without any assistance
- Able to follow the study protocol
- Fluent in English and able to provide informed consent
EXCLUSION CRITERIA:
- History of exercise intolerance
- History of heart disease
- History of pulmonary disease, other than controlled, non-exercise-induced asthma
- History of uncontrolled diabetes
- Uncontrolled hypertension, defined as a resting blood pressure > 140/90 mmHg
- On medications that would influence aerobic capacity or treadmill performance such as beta blockers or antiretroviral therapy
- Active substance abuse including ETOH
- Presence of an injury to any extremity, or other medical condition that would affect motor function or the ability to perform the assessment or the exercise program, specifically balance problems due to vestibulopathy
- Unable to refrain from smoking at least 4 hours prior to exercise testing sessions
- Medical or psychological instability such that the subject could not reasonably be expected to fulfill the study requirements
- Pregnancy
- BMI >40 kg/M(2) due to the limits of the treadmill, elliptical machine and MRI scanner
- Planning to make a change in medication or therapy during the enrollment period with the goal of improving mood, cognitive function or motor function
Have any of the following contraindications to having an MRI scan:
- A ventriculo-peritoneal shunt
- Have claustrophobia and not comfortable in small enclosed spaces
- Have metal that would make an MRI scan unsafe such as: cardiac pacemaker, insulin infusion pump, implanted drug infusion devise, cochlear or ear implant, transdermal medication patch (nitroglycerine), any metallic implants or objects, body piercing that cannot be removed, bone or joint pin, screw, nail, plate, wire sutures or surgical staples, shunts, cerebral aneurysms clips, shrapnel or other metal embedded (such as from war wounds or accidents or previous work in metal fields or machines that may have left any metallic fragments in or near your eyes).
- Excessive startle reaction to or fear of loud noises
Sites / Locations
- National Institutes of Health Clinical Center
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Experimental
No Intervention
No Intervention
Experimental
Arm Label
AET
Control
Healthy Volunteer
RET
Arm Description
Aerobic exercise will be performed on an elliptical trainer at a vigorous intensity
Wait-list control that performs no exercise for first 12 weeks; randomized to an exercise intervention (either AET or RET) after 12 weeks
Healthy volunteers will perform specific measures for a single study visit
Rapid reciprocal exercise will be performed on an elliptical trainer at light to moderate intensity
Outcomes
Primary Outcome Measures
Change in cognitive function (TMT-B)
The difference in the time taken to complete the Trail Making Test B reflects the change in a subjects level of executive function.
Secondary Outcome Measures
Change in motor assessment
Change in cardiorespiratory fitness
Change in fatigue
Change in biomarkers
Change in structural and functional measures (MRI)
Change in other measures of cognitive function
Comparison of imaging, biomarkers, cognitive and behavioral measures to healthy volunteers
Full Information
NCT ID
NCT02504866
First Posted
July 21, 2015
Last Updated
April 10, 2023
Sponsor
National Institutes of Health Clinical Center (CC)
1. Study Identification
Unique Protocol Identification Number
NCT02504866
Brief Title
Effect of Exercise Training on Physical, Cognitive, and Behavioral Function in People With TBI
Official Title
Effect of Exercise Training on Physical, Cognitive and Behavioral Function in Patients With Traumatic Brain Injury
Study Type
Interventional
2. Study Status
Record Verification Date
February 14, 2023
Overall Recruitment Status
Completed
Study Start Date
December 15, 2016 (Actual)
Primary Completion Date
December 31, 2022 (Actual)
Study Completion Date
January 23, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Institutes of Health Clinical Center (CC)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Background:
- Traumatic brain injury (TBI) often causes problems with moving and balance, and thinking and emotions. Exercise can improve these things in people with other brain damage. Researchers want to look at the effect of exercise on these things in people with TBI.
Objectives:
- To study how head injuries affect the brain. To study if exercise can help some symptoms in people with TBI. These include problems thinking, balancing, and moving, and depression or anxiety.
Eligibility:
People age between 18 and 79 :
Had a non-penetrating TBI at least 12 months ago.
Are physically inactive, but can stand and walk without help.
Design:
Participants will be screened with medical history, physical exam, and blood and urine tests. They may have a balance test.
Participants will be assigned to a high-intensity or a lower-intensity exercise program.
The study is 6 months long. There will be 3 months with exercise on an elliptical machine and 3 months without exercise.
Participants will exercise for 30 minutes on an elliptical machine, 3 days per week for 3 months.
Participants will also have 3 outpatient testing visits lasting approximately 8 hours, once every 3 months. This visit will include:
Blood tests
Tests for memory, attention, and thinking
Tests of walking and balance
Questionnaires
An MRI: they will lie in a machine that takes pictures of their brain, while breathing regular air and air with more carbon dioxide
Test of physical fitness.
Detailed Description
Objective
The broad objective of this study is to examine the effects of moderate and more intense aerobic exercise as an intervention on cognitive performance, physical functioning and health-related quality of life in patients with chronic (more than 12 months post-injury) traumatic brain injury (TBI). Importantly, structural and biological brain changes will be measured to examine whether functional outcomes are related to exercise-induced adaptations. It is hypothesized that in the chronic phase of persons with TBI, there will be improved: 1) cognitive function, 2) physical fitness and fatigue severity, 3) motor performance and balance, and 4) mood and depressive symptoms, in those that performed the exercise intervention compared to a control group. It is also hypothesized that these functional improvements will be related to exercise intensity, improved cortical connectivity, dopamine transmission gene scores, and blood biomarkers related to neuroand angio-genesis.
Study Population
80 ambulatory adults with non-penetrating TBI will be enrolled. We will also enroll up to 20 healthy volunteers as a comparison group for some of the outcome measures. Subjects will be recruited from NIH, affiliated hospitals/clinics and the community
Design
Healthy volunteers will have a limited assessment that includes brain imaging, blood draw for genetic testing, and a subset of the cognitive and behavioral testing at a single time-point. All subjects with TBI will perform baseline assessments including cognitive and behavioral performance, brain imaging, fitness, motor and balance testing, and selected blood and genetic testing. Thereafter, subjects with TBI will be randomized to either a waitlist control, or one of two exercise conditions: 1) 30 minutes at a fast pace, moderate-intensity (rapidresistive exercise; RET); 2) 30 minutes at higher-intensity (aerobic exercise; AET). Both exercise groups will perform the exercise on an elliptical trainer 3 times a week, for a session duration of 45 minutes including warm-up and cool-down. The RET group will focus on rapid reciprocal motion with minimal resistance, while the AET group will exercise at an elevated intensity known to produce an aerobic effect. After 12 weeks, all groups will repeat the baseline assessments (3 month follow-up). Following this assessment, the waitlist control group will be randomized to either RET or AET and the exercise groups will cease formal supervised exercise sessions. A third assessment visit will be performed after an additional 12 weeks (6 month follow-up).
Outcome Measures
Cognitive performance will be tested and interpreted compared to norms. Performance on motor and balance tasks will be assessed with the Smart Balance Measurement System and the GAITRite System. Physical fitness will be determined by peak oxygen consumption and aerobic threshold as measured by pulmonary gas exchange during an exercise tolerance test on the treadmill. Structural brain volumes will be determined by magnetic resonance imaging (MRI) and cortical connectivity will be quantified using resting state functional MRI and Diffusion Tensor Imaging (DTI) to evaluate integrity of and changes in white matter tracts in response to exercise and compared to healthy volunteers. Blood will be collected to quantify the presence of biomarkers (such as VEGF, BDNF and IGF-1) and dopamine transmission. Other self-reported measures of quality of life, fatigue severity, depression and sleep quality would also be collected, and compared to healthy volunteers.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Traumatic Brain Injury
Keywords
Aerobic Exercise Training, Balance, TBI
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Arm Title
AET
Arm Type
Experimental
Arm Description
Aerobic exercise will be performed on an elliptical trainer at a vigorous intensity
Arm Title
Control
Arm Type
No Intervention
Arm Description
Wait-list control that performs no exercise for first 12 weeks; randomized to an exercise intervention (either AET or RET) after 12 weeks
Arm Title
Healthy Volunteer
Arm Type
No Intervention
Arm Description
Healthy volunteers will perform specific measures for a single study visit
Arm Title
RET
Arm Type
Experimental
Arm Description
Rapid reciprocal exercise will be performed on an elliptical trainer at light to moderate intensity
Intervention Type
Other
Intervention Name(s)
Exercise
Intervention Description
Exercise training of different intensity
Primary Outcome Measure Information:
Title
Change in cognitive function (TMT-B)
Description
The difference in the time taken to complete the Trail Making Test B reflects the change in a subjects level of executive function.
Time Frame
Baseline, 3 months, 6 months
Secondary Outcome Measure Information:
Title
Change in motor assessment
Time Frame
Baseline, 3 months, 6 months
Title
Change in cardiorespiratory fitness
Time Frame
Baseline, 3 months, 6 months
Title
Change in fatigue
Time Frame
Baseline, 3 months, 6 months
Title
Change in biomarkers
Time Frame
Baseline, 3 months, 6 months
Title
Change in structural and functional measures (MRI)
Time Frame
Baseline, 3 months, 6 months
Title
Change in other measures of cognitive function
Time Frame
Baseline, 3 months, 6 months
Title
Comparison of imaging, biomarkers, cognitive and behavioral measures to healthy volunteers
Time Frame
Baseline
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
79 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
INCLUSION CRITERIA:
Inclusion criteria for those with TBI:
Ages 18 to 79 inclusive
Diagnosis of non-penetrating TBI
Injury occurred at least 12 months prior to enrollment
Physically inactive as identified by a physician
Able to stand and walk independently and safely without any assistance
Able to follow the study protocol
Fluent in English and able to provide informed consent
Inclusion criteria for healthy volunteers:
Ages 18 to 79 inclusive
Physically inactive as identified by a physician
Fluent in English
EXCLUSION CRITERIA:
Exclusion criteria for those with TBI:
History of exercise intolerance
History of heart disease
History of pulmonary disease, other than controlled, non-exercise-induced asthma
History of uncontrolled diabetes
Uncontrolled hypertension, defined as a resting blood pressure > 140/90 mmHg
On medications that would influence aerobic capacity or treadmill performance such as beta blockers or antiretroviral therapy
Active substance abuse including ETOH
Presence of an injury to any extremity, or other medical condition that would affect motor function or the ability to perform the assessment or the exercise program, specifically balance problems due to vestibulopathy
Unable to refrain from smoking at least 4 hours prior to exercise testing sessions
Medical or psychological instability such that the subject could not reasonably be expected to fulfill the study requirements
Pregnancy
BMI >40 kg/M(2) due to the limits of the treadmill, elliptical machine and MRI scanner
Planning to make a change in medication or therapy during the enrollment period with the goal of improving mood, cognitive function or motor function
Have any of the following contraindications to having an MRI scan:
A ventriculo-peritoneal shunt
Have claustrophobia and not comfortable in small enclosed spaces
Have metal that would make an MRI scan unsafe such as: cardiac pacemaker, insulin infusion pump, implanted drug infusion devise, cochlear or ear implant, transdermal medication patch (nitroglycerine), any metallic implants or objects, body piercing that cannot be removed, bone or joint pin, screw, nail, plate, wire sutures or surgical staples, shunts, cerebral aneurysms clips, shrapnel or other metal embedded (such as from war wounds or accidents or previous work in metal fields or machines that may have left any metallic fragments in or near your eyes).
Excessive startle reaction to or fear of loud noises
Exclusion criteria for healthy volunteers:
History or presence of cardiopulmonary or respiratory disease
History or presence of other disease of the neurologic, metabolic, or renal systems
Active substance abuse including ETOH
Pregnancy
BMI >40 kg/m2
Medical or psychological instability such that the subject could not reasonably be expected to fulfill the study requirements
Have any contraindications to having an MRI scan
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Diane L Damiano, Ph.D.
Organizational Affiliation
National Institutes of Health Clinical Center (CC)
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Institutes of Health Clinical Center
City
Bethesda
State/Province
Maryland
ZIP/Postal Code
20892
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
25433219
Citation
Chin LM, Keyser RE, Dsurney J, Chan L. Improved cognitive performance following aerobic exercise training in people with traumatic brain injury. Arch Phys Med Rehabil. 2015 Apr;96(4):754-9. doi: 10.1016/j.apmr.2014.11.009. Epub 2014 Nov 26.
Results Reference
background
PubMed Identifier
24901330
Citation
Chin LM, Chan L, Woolstenhulme JG, Christensen EJ, Shenouda CN, Keyser RE. Improved Cardiorespiratory Fitness With Aerobic Exercise Training in Individuals With Traumatic Brain Injury. J Head Trauma Rehabil. 2015 Nov-Dec;30(6):382-90. doi: 10.1097/HTR.0000000000000062.
Results Reference
background
Links:
URL
https://clinicalstudies.info.nih.gov/cgi/detail.cgi?B_2015-CC-0164.html
Description
NIH Clinical Center Detailed Web Page
Learn more about this trial
Effect of Exercise Training on Physical, Cognitive, and Behavioral Function in People With TBI
We'll reach out to this number within 24 hrs