Modulation of Brain Oscillations Underlying Working Memory

Sponsor
Massachusetts General Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05923606
Collaborator
(none)
32
1
4
36
0.9

Study Details

Study Description

Brief Summary

This study will use novel transcranial alternating current stimulation (tACS) protocols and electroencephalography (EEG) to modulate and measure brain oscillations that underlie working memory. tACS is a noninvasive method used to modulate the timing and patterns of brain rhythms via weak electric currents passed through electrodes on the scalp.

Condition or Disease Intervention/Treatment Phase
  • Device: Active tACS
  • Device: Placebo tACS
N/A

Detailed Description

In this study, healthy adult individuals will perform a spatial working memory task as we record scalp EEG before and immediately after undergoing transcranial alternating current stimulation (tACS). Each participant will complete four tACS sessions in randomized order: 1) theta-nested gamma tACS applied during active task periods, 2) theta-nested gamma tACS applied during passive (rest) periods, 3) gamma stimulation applied in phase with ongoing theta oscillations, and 4) placebo tACS. The different stimulation protocols will take place on different days. Therefore, participants will be expected to attend 4 in-person study visits at the Martinos Center for Biomedical Imaging in Charlestown, Massachusetts.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
32 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Basic Science
Official Title:
State-dependent Modulation of Interactions of Theta and Gamma Rhythms in Working Memory
Anticipated Study Start Date :
Sep 1, 2023
Anticipated Primary Completion Date :
Aug 31, 2025
Anticipated Study Completion Date :
Aug 31, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: Theta-nested gamma tACS applied during passive task epochs

Participants will receive single-session administration of tACS during performance of a working memory task. tACS will be applied during fixation periods between consecutive task trials. EEG will be acquired before and immediately after the intervention.

Device: Active tACS
Active tACS will be administered over the left dorsolateral prefrontal cortex for approximately 25 minutes.

Experimental: Theta-nested gamma tACS applied during memory delays

Participants will receive single-session administration of tACS during performance of a working memory task. tACS will be applied during memory delays. EEG will be acquired before and immediately after the intervention.

Device: Active tACS
Active tACS will be administered over the left dorsolateral prefrontal cortex for approximately 25 minutes.

Experimental: Gamma tACS applied during memory delays

Participants will receive single-session administration of tACS during performance of a working memory task. tACS will be applied during memory delays. The stimulation will be phase locked to the peaks of ongoing theta rhythms of the participant. EEG will be acquired before and immediately after the intervention.

Device: Active tACS
Active tACS will be administered over the left dorsolateral prefrontal cortex for approximately 25 minutes.

Placebo Comparator: Placebo tACS applied during task performance

Participants will receive single-session administration of placebo tACS during performance of a working memory task. EEG will be acquired before and immediately after the intervention.

Device: Placebo tACS
Placebo tACS will be administered over the left dorsolateral prefrontal cortex for approximately 25 minutes.

Outcome Measures

Primary Outcome Measures

  1. Working memory accuracy [2 hours]

    Accuracy of working memory retrieval during a Delayed Match-to-Sample task will be assessed before and during tACS interventions

  2. Working memory accuracy under interference [2 hours]

    Accuracy of working memory retrieval during interference conditions of a Delayed Match-to-Sample task will be assessed before and during tACS interventions.

  3. Theta-gamma cross-frequency coupling [2 hours]

    Cross-frequency coupling between theta band phase and gamma band amplitude will be calculated using the EEG data collected while subjects perform the Delayed Match-to-Sample task before and after tACS interventions.

  4. Fronto-parietal theta phase synchronization [2 hours]

    Phase synchronization in the theta band between frontal and parietal brain regions will be calculated using the EEG data collected while subjects perform the Delayed Match-to-Sample task before and after the tACS interventions.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 35 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Able to provide informed consent

  • Fluent in English.

Exclusion Criteria:
  • History of a neurological/psychiatric disorder

  • Current use of psychotropic medications

  • Current use of substances and drugs that were shown to affect tES (transcranial electrical stimulation) efficacy (dopamine altering drugs, nicotine, NMDA (N-methyl-D-aspartate) antagonists/agonists, sodium/calcium channel blockers, norepinephrine reuptake inhibitors, GABAergic modulators and selective serotonin reuptake inhibitors)

  • Contraindications for tACS (e.g., history of seizures, metallic implants in the head or neck, implanted brain stimulators, vagus nerve stimulators, pacemakers, pregnancy)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Martinos Center for Biomedical Imaging Charlestown Massachusetts United States 02129

Sponsors and Collaborators

  • Massachusetts General Hospital

Investigators

  • Principal Investigator: Hamdi Eryilmaz, Ph.D., Massachusetts General Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hamdi Eryilmaz, PhD, Assistant Professor, Massachusetts General Hospital
ClinicalTrials.gov Identifier:
NCT05923606
Other Study ID Numbers:
  • 2023P001479
First Posted:
Jun 28, 2023
Last Update Posted:
Jun 28, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Keywords provided by Hamdi Eryilmaz, PhD, Assistant Professor, Massachusetts General Hospital

Study Results

No Results Posted as of Jun 28, 2023