no participants enrolled due to COVID

Transcranial electrical stimulation (tES) is a non-invasive form of brain stimulation that has previously been to shown to have therapeutic potential in traumatic brain injury (TBI) patients. In this study, the study team will use a brain activity monitor (electroencephalogram, EEG) and a computer-based task to observe the effects of different forms of tES, like transcranial direct current stimulation (tDCS) and transcranial pulsed current stimulation (tPCS), on impulse control and sustained attention in people with TBI. Additionally, the study team will measure how much tDCS and tPCS affect the brain activity of a specific area of the brain associated with impulse control and attention. Problems with response inhibition have been shown to make rehabilitation more difficult for people with TBI. It also reduces social functioning and can also negatively affect job performance, which ultimately lead to a decreased quality of life. A better understanding of the effects of tES in TBI patients could be informative in finding out what its therapeutic potential is for this population.

Inclusion Criteria:

• Subjects referred to the PI for management of TBI
• Subject is at least 3 months post-injury at the time of consent
• Ages 25-70

Exclusion Criteria:

• Subjects with the inability to consent for themselves
• Subjects with body habitus that does not allow the EEG cap to be properly placed
• Presence of scalp injury or disease
• Allergic reaction to topical lidocaine jelly
• Prior intracranial surgery or skull-fracture over VLPFC
• Presence of hemorrhage on intracranial imaging
• Prior brain radiotherapy
• Prior history of intracranial tumor, intracranial infection, or cerebrovascular malformation
• Subjects with the inability to see and read from a computer screen
• History of any form of seizures prior to TBI or within 6 months of study participation
• Pregnancy

Individual participant data that underlie the results reported in this article, after deidentification may be shared as well as the study protocol, statistical analysis plan, and analytic code.

Immediately following publication. No end date.

For analyses to achieve aims in the approved proposal accessible by contacting the study principal investigator.