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Cerebral Excitability and Cognitive Performance

Cerebral Excitability and Cognitive Performance

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03807934
Enrollment
1500
Registered
2019-01-17
Start date
2013-04-15
Completion date
2023-04-14
Last updated
2021-04-05

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

Conditions

Cognitive Change

Keywords

transcranial direct current stimulation, cognitive psychology, noninvasive brain stimulation, electrical brain stimulation

Brief summary

This study investigates the perceptual and cognitive influences of low-intensity electrical brain stimulation (transcranial direct current stimulation; tDCS), versus control (sham) conditions.

Interventions

OTHERStimulation via Soterix Medical or Neuroelectrics noninvasive brain stimulation systems

Active (at or below 2mA) versus sham (at or below 0.5mA) stimulation targeting brain regions engaged during verbal and/or spatial perceptual and cognitive processing. Brain stimulation devices are not currently regulated by the United States Food and Drug Administration. Local IRB has determined the devices to be non-significant risk (NSR) devices via abbreviated investigational device exemption (IDE) procedure.

Sponsors

Tufts University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Intervention model description

Repeated-measures crossover design.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

\- Between ages of 18-65.

Exclusion criteria

* History of adverse reaction to tDCS (trans-cranial direct current stimulation). * History of seizure activity. * History of head injury (including neurosurgery). * History of illness causing brain injury. * History of other brain-related condition (such as traumatic brain injury). * History of diagnosis with a neurological or psychiatric disorder. * History of metal in head (outside of mouth), such as shrapnel, surgical clips, or fragments from welding or metalwork. * History of sensitive scalp.

Design outcomes

Primary

MeasureTime frameDescription
Visual perceptual performance36 weeksAbility to accurately and efficiently perceive perceptual information, including threat detection, local contrast gradient detection, face memory, and intent appraisal. All are computerized tasks.
Verbal cognitive performance36 weeksAbility to accurately and efficiently process verbal information, including verbal cued free association tasks, verbal long-term memory, and language comprehension. All are computerized tasks.
Spatial cognitive performance72 weeksAbility to accurately and efficiently process spatial information, including map learning, virtual urban navigation, and mental rotation. All are computerized tasks.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026