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At Home Brain Stimulation Studies of Memory and Memory Awareness

At Home Brain Stimulation Studies of Memory and Memory Awareness

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04749719
Acronym
remTDCS
Enrollment
36
Registered
2021-02-11
Start date
2021-04-15
Completion date
2023-08-21
Last updated
2021-07-12

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

Conditions

Healthy

Keywords

transcranial direct current stimulation, memory, metacognition, brain

Brief summary

The main goal of this research is to determine the role of several brain regions in memory processes and cognitive functions. Participants will be remotely supervised via video chat while self-administering tDCS, a form of non-invasive brain stimulation. Before participating in the experiment, participants will be properly trained on use of the remote tDCS device and screened for eligibility. While using the tDCS device, participants will be engaging in tasks that assess different aspects of memory and executive functioning. By using remotely supervised tDCS while participants are completing these cognitive tasks, we will be able to make causal claims about the role of the targeted brain regions in different cognitive processes.

Interventions

DEVICEremotely supervised transcranial direct current stimulation

Low levels of electrical current are applied across the scalp to induce small changes in brain activity. This is done using remote supervision.

Sponsors

National Institute of General Medical Sciences (NIGMS)
CollaboratorNIH
Brooklyn College of the City University of New York
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* between the ages of 18-35 * normal or corrected to normal vision * fluent in English and speaking English since age 5 * right handed

Exclusion criteria

* chronic skin disease or medical skin condition * unhealed wound or open skin on the scalp, face, neck, or forehead * metal or electrode implants (e.g., cochlear implants, pacemakers, metal plates, rods, or screws in their head; for complete detail, see the screening form) * seizures or a family history of seizures, or are taking medications with a lowered seizure threshold * pregnant or lactating * any neurologic or psychiatric diseases * certain hair styles (dreadlocks, cornrows, etc) or hair coverings (e.g., wigs, hajibs, etc that will not be removed; note that a request can be made for an experimenter of a specific gender)

Design outcomes

Primary

MeasureTime frameDescription
Memory performancethrough study completion, an average of 4 weeks% Correct on the Memory Task

Secondary

MeasureTime frameDescription
Memory Confidencethrough study completion, an average of 4 weeksAverage % Confidence on the Memory Task

Other

MeasureTime frameDescription
Metamemory Accuracythrough study completion, an average of 4 weeksCalibration and resolution of confidence and accuracy.

Countries

United States

Contacts

Primary ContactELIZABETH CHUA, PHD
echua@brooklyn.cuny.edu7189515000
Backup ContactCasey Imperio, MS
cimperio@gradcenter.cuny.edu6098464723

Outcome results

None listed

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