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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04239274
Other study ID # 00093356
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date January 1, 2020
Est. completion date January 1, 2021

Study information

Verified date December 2021
Source Medical University of South Carolina
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date January 1, 2021
Est. primary completion date January 1, 2021
Accepts healthy volunteers No
Gender All
Age group 25 Years to 70 Years
Eligibility 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

Study Design


Intervention

Device:
transcranial direct current stimulation
Subjects in this arm will receive one session of tDCS for 20 minutes at 2.0 milliamps.
transcranial pulsed current stimulation
Subjects in this arm will receive one session of tPCS for 20 minutes at 2.0 milliamps.
Sham-no stimulation
Subjects in this arm will receive one session of sham for 20 minutes.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Medical University of South Carolina

Outcome

Type Measure Description Time frame Safety issue
Primary Average Reaction Time During Stop Signal Task The Stop Signal Task (SST) is an assessment which requires participants to respond to various stimuli with a specific action and to not respond when a "stop" stimulus is presented. Throughout study (1 hour)
Primary EEG power in all frequency bands They will be fitted with a standard EEG cap consisting of 32 EEG electrodes placed in the 10/20 international system format, a standardized system for EEG electrode placement. Frequency bands will be measured. Baseline and immediately post Stimulation
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