Skip to main content
Clinical Trials/NCT01602263
NCT01602263
Completed
Not Applicable

Transcranial Direct Current Stimulation (tDCS)and Cognitive Processing

Johns Hopkins University1 site in 1 country307 target enrollmentJanuary 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Aphasia
Sponsor
Johns Hopkins University
Enrollment
307
Locations
1
Primary Endpoint
Indices of cognitive function
Status
Completed
Last Updated
3 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
January 2009
End Date
March 2, 2023
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

Indices of cognitive function

Time Frame: The average time frame is 1 hour

Secondary Outcomes

  • Initiation, endurance and cessation of skin sensations caused by tDCS(The average time frame is 1 hour)
  • Persistence of cognitive enhancements following tDCS(The average time frame is 1 hour)

Study Sites (1)

Loading locations...

Similar Trials