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Awareness of Deficit After Combat-related Brain Injury

Awareness of Deficit After Combat-related Brain Injury

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00478400
Enrollment
100
Registered
2007-05-24
Start date
2007-10-01
Completion date
2016-10-31
Last updated
2017-12-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Traumatic Brain Injury, Veterans

Keywords

Recovery, Magnetic resonance imaging, Awareness, Neurologic deficits

Brief summary

This study will use MRI imaging, cognitive testing and outcome questionnaires to determine how the brain recovers and reorganizes after an injury.

Detailed description

The extent of recovery from brain injury is often difficult to predict because of our limited understanding of how the brain changes as it heals. New brain imaging methods may help in this regard. One imaging technique called functional magnetic resonance imaging (fMRI) has made it possible to study the brain at work; that is, we can see regions of the brain that are active during particular tasks such as focusing attention, making decisions, or remembering words and pictures. Another MRI method called diffusion tensor imaging provides information on the pathways between brain regions that may be altered with brain injury. The goals of this research are to 1) determine the brain regions involved in making accurate judgments about one's abilities and disabilities after a brain injury and whether damage to these brain areas affects outcome; and 2) examine how recovery of cognitive and physical abilities relates to changes in brain function over time. In order to accomplish the first goal we will recruit Veterans who have sustained a head injury and matched control subjects. For the second goal, we are asking patients and controls who have previously participated in brain injury research with our lab to come back for another visit at three years post-injury.

Interventions

None listed

Sponsors

University of Wisconsin, Madison
CollaboratorOTHER
VA Office of Research and Development
Lead SponsorFED

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years

Inclusion criteria

* History of traumatic brain injury at least 12 months prior to enrollment * Control Group: No history of traumatic brain injury

Exclusion criteria

* Claustrophobia * Metallic or electronic implants or devices that are not MRI-safe * Foreign metal, such as shrapnel, in the body

Design outcomes

Primary

MeasureTime frameDescription
Cognition change at study endpoint between TBI and controlsGreater than 3 years post-injury
Longitudinal change in white matter2 months, 1 year, and greater than 3 years post-injuryParticipants will include post-TBI in survivors the investigators have studied previously
Longitudinal change in whole brain morphology2 months, 1 year, and greater than 3 years post-injuryParticipants will include post-TBI in survivors the investigators have studied previously

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026