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The Effects of Transcranial Direct Current Stimulation (tDCS) and Cognitive Training in Patients With TBI

The Effects of Transcranial Direct Current Stimulation (tDCS) and Cognitive Training on Episodic Memory and Attention in Patients With Traumatic Brain Injury: a Double-blind, Randomized, Placebo-controlled Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04540783
Enrollment
36
Registered
2020-09-07
Start date
2020-09-01
Completion date
2022-12-01
Last updated
2020-09-07

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

Conditions

Closed Traumatic Brain Injury, Severe Brain Injury, Traumatic Brain Injury

Brief summary

Long-term sequelae in TBI is a well-recognized burn. We designed a proof of concept study, randomized, double-blind, placebo-controlled to evaluate 36 adult TBI patients. To evaluate the early and late effects of 10 days of 20 minutes applying transcranial direct-current stimulation (tDCS) in the dorsolateral prefrontal cortex (DLPFC), bilateral temporal cortex (CTB) and compare to sham stimulation, and online cognitive training. We expect that the active group will differ from the sham group, showing larger effect sizes in the cognitive assessment.

Detailed description

Method: proof of concept study, randomized, double-blind, placebo-controlled. 36 adult patients will be recruited, with closed TBI for at least 6 months, of both sexes. The sequence of randomization will provide the allocation 1: 1: 1 in parallel groups: G1 n = 12 active (CTB), G2 n = 12 active (DLPFC), and G3 n = 12 (Sham). The tDCS will be held with the intensity of 2 mA for 20 minutes per session and online cognitive training (concurrent with the ETCC). All patients, after the screening and randomization, will make a baseline neuropsychological assessment (T0) and receive 10 sessions of stimulation concomitant to cognitive training. Patients will undergo neuropsychological reassessment one week (T1) and two months (T2) after the last tDCS session. We will evaluate performance on episodic memory tests, working memory and attention in the three periods (T0, T1, and T2). The significance adopted is the level of 5% (α = 0.05), analysis of 80% power and bicaudal curve. Analysis of the results will be done by intention to treat (ITT).

Interventions

DEVICETranscranial direct current stimulation (tDCS)

10 sessions of 2mA and 20 minutes tDCS. Sponges size 5x7 cm. For the sham condition, the patient will receive just 30 seconds of stimulation.

Sponsors

University of Sao Paulo General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

sham device (by code)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

clinical diagnosis closed traumatic brain injury, cognitive complaints reported by the patient or caregiver.

Exclusion criteria

metal implants in the head, seizures, abnormal EEG, depressive symptoms

Design outcomes

Primary

MeasureTime frameDescription
Episodic Memory measured by The Rey Auditory-Verbal Learning Test (RAVLT)up to 2 weeksList of words

Secondary

MeasureTime frameDescription
Memory cognitive trainingup to 2 weeksThe patients will receive 10 days of episodic memory training.
Attention cognitive trainingup to 2 weeksThe patients will receive 10 days of attention training.

Other

MeasureTime frameDescription
electroencephalogram - EEGup to 2 weekselectroencephalogram will be used for safety (Alpha and delta wave)

Countries

Brazil

Contacts

Primary ContactWellingson S Paiva, MD PhD
wellingsonpaiva@yahoo.com.br+5511975992245
Backup ContactManoel J Teixeira, MD PhD
manoeljacobsen@gmail.com+551126610000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026