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Transcranial Direct Current Stimulation (tDCS) and Cognitive Processing

Transcranial Direct Current Stimulation (tDCS)and Cognitive Processing

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01602263
Enrollment
307
Registered
2012-05-18
Start date
2009-01-31
Completion date
2023-03-02
Last updated
2023-03-07

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

Conditions

Aphasia, Autism, Schizophrenia

Keywords

Normal cognitive function, Aphasia, Autism, Schizophrenia

Brief summary

This research is being done to determine whether transcranial direct current stimulation (tDCS) can improve certain mental abilities. In this research, battery powered device is used to deliver very weak electrical current to the surface of the scalp while participants complete cognitive tasks. Our aim is to find out whether tDCS will improve task performance in both healthy adults and those with neurological impairment.

Detailed description

Participants enrolled into this study may be asked to do the following: * Grant permission for the researchers to view medical records associated with their language/cognitive difficulties (if applicable. * Complete a questionnaire, provide a health history, and take some pencil-and-paper tests of problem-solving and memory in order to verify eligibility to participate and to able to safely undergo the experimental procedures. * Complete several tasks (i.e., saying words out loud, naming objects, drawing designs, remembering lists of words, searching for images or letters, and/or completing puzzles) based upon a number of cognitive functions such as language, memory, vision, processing, and perception. * Wear electrodes that will be placed on the scalp with a large rubberized band. These electrodes will administer very weak electrical current (tDCS) from a battery powered device for 20 to 60 minutes. * Participation in several study conditions. The exact conditions and their order will be randomized. Under some conditions, participants may receive active stimulation (tDCS) and under other conditions, they may receive sham stimulation. * The experimental sessions will last approximately 2 hours and participants may be asked to have more than one testing session in a day or to return for additional sessions. * Have a Magnetic Resonance Imaging (MRI) brain scan.

Interventions

PROCEDURETranscranial Direct Current Stimulation (tDCS)

Anodal, Cathodal or Sham tDCS.

Sponsors

Johns Hopkins University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 79 Years
Healthy volunteers
Yes

Inclusion criteria

Eligibility Criteria by Study Group Normal Controls Inclusion Criteria: * Right handed (as determined by the Edinburgh battery) * English as native language Normal Controls

Exclusion criteria

* Appreciable deficits in hearing * Appreciable problems with articulation * Schizophrenia, bipolar disorder, or major depression * Appreciable accent * Any neurological disorder associated with cognitive impairment or neuroanatomic abnormality * Language-based learning disorder * Any implanted metal device (precludes use of tDCS) * Any implanted cardiac pacemaker * Dementia or Mini-Mental State Exam \< 24 * Estimated verbal intelligence \< 70 Aphasia Group Inclusion Criteria: * Right handed (as determined by the Edinburgh battery) * English as native language * History of acquired left-hemisphere dysfunction Aphasia Group

Design outcomes

Primary

MeasureTime frame
Indices of cognitive functionThe average time frame is 1 hour

Secondary

MeasureTime frameDescription
Persistence of cognitive enhancements following tDCSThe average time frame is 1 hour
Initiation, endurance and cessation of skin sensations caused by tDCSThe average time frame is 1 hourThe initiation, endurance and cessation of skin sensations caused by tDCS will be examined in order to develop a more effective blinding procedure.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026