Effects of Brain-stimulation on Metamemory Monitoring and Control

NCT ID: NCT03693729

Last Updated: 2020-07-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

216 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-09-03

Study Completion Date

2022-06-30

Brief Summary

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When people learn and remember information, it is often accompanied by a feeling of subjective confidence about whether or not information has been learned and accurately remembered. These subjective feelings of confidence are often related to actual memory performance, but are sometimes incorrect. The investigators have previously shown that applying high definition transcranial direct current stimulation (HD-tDCS) over the dorsolateral prefrontal cortex leads to more accurate feelings of subjective confidence, at least when subjects are asked for their confidence about future memory performance. Accurate confidence judgments are useful in that they may later subsequent behavior, and inaccurate ones may be costly. For example, a student who erroneously believes that studied material was learned may stop studying and not do well on a test. Individuals who have a feeling-of-knowing about the answer to a general knowledge question will continue to search their memory, whereas individuals who do not have a feeling-of-knowing will stop searching their memory. Individuals who are confident they know the answer to a question are more likely to answer it. In this study, the experimenters are testing the effects of brain stimulation on subjective awareness of memory (termed metamemory monitoring) and how people use those subjective judgments (termed metamemory control). The approach taken is to have participants visit the laboratory on 3 visits and receive brain stimulation while completing memory and metamemory tasks.

Detailed Description

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Conditions

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Healthy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

SINGLE

Participants

Study Groups

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Active DLPFC during task

HD-tDCS will be applied over the DLPFC at 2mA in a single session for up to 30 min during the memory and metamemory task

Group Type EXPERIMENTAL

HD-tDCS

Intervention Type DEVICE

Participants will complete a metamemory and memory task

Active DLPFC after task

HD-tDCS will be applied over the DLPFC at 2mA in a single session for up to 30 min after the memory and metamemory task and during a filler task.

Group Type ACTIVE_COMPARATOR

HD-tDCS

Intervention Type DEVICE

Participants will complete a metamemory and memory task

Sham DLPFC during task

Sham HD-tDCS will be applied over the DLPFC at 2mA in a single session for up to 30 min during the memory and metamemory task

Group Type SHAM_COMPARATOR

HD-tDCS

Intervention Type DEVICE

Participants will complete a metamemory and memory task

Interventions

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HD-tDCS

Participants will complete a metamemory and memory task

Intervention Type DEVICE

Other Intervention Names

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Behavioral

Eligibility Criteria

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Inclusion Criteria

* Healthy, right-handed adults ages 18-35. English spoken since age 5. Normal or corrected-to-normal vision.

Exclusion Criteria

* Participants will be excluded if they have chronic skin disease or a medical skin condition, or an unhealed open wound on the scalp, face, neck, or forehead near the electrode location.
* Participants will be excluded if they self-report significant medical, neurological, or psychiatric illness and/or a history of substance abuse
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Institute of General Medical Sciences (NIGMS)

NIH

Sponsor Role collaborator

Brooklyn College of the City University of New York

OTHER

Sponsor Role lead

Responsible Party

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Elizabeth Chua

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Brooklyn College

Brooklyn, New York, United States

Site Status

Countries

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United States

Other Identifiers

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SC3GM121192

Identifier Type: NIH

Identifier Source: secondary_id

View Link

BrooklynC

Identifier Type: -

Identifier Source: org_study_id

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