Causal Role of Brain Networks in Episodic Memory
1 other identifier
interventional
41
1 country
1
Brief Summary
The goal of this study is to understand the basic brain mechanisms supporting episodic memory in healthy young adults. Transcranial magnetic stimulation will be used to influence brain activity in regions thought to be important for episodic memory. Behavioral testing and MRI will be used to measure the effects of stimulation on memory and on changes in brain network interactions, allowing us to draw causal inferences regarding the role of specific brain regions in memory processes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Oct 2023
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 29, 2022
CompletedFirst Posted
Study publicly available on registry
May 16, 2022
CompletedStudy Start
First participant enrolled
October 6, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2025
CompletedFebruary 25, 2026
February 1, 2026
2.2 years
April 29, 2022
February 24, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Accuracy on tests of episodic memory
Participants will complete tasks where they encode and retrieve events. Episodic memory quality will be assessed as the accuracy with which they can recall scene details associated with each event.
Tasks will be completed during the hour following stimulation.
Task-related functional connectivity among posterior medial brain regions
Psychophysiological interaction analyses will be used to assess task-related functional connectivity while participants complete the memory retrieval task. This will identify interactions among brain regions that are associated with successful memory retrieval.
Functional connectivity will be assessed during the hour following stimulation.
Study Arms (1)
All participants
OTHERAll participants will complete all experimental conditions, which include transcranial magnetic stimulation (continuous theta-burst stimulation) to a brain region of experimental interest and to a control brain region.
Interventions
Transcranial magnetic stimulation will be used to stimulate brain activity in a brain region of experimental interest (lateral parietal cortex) and in a control brain region (vertex). All participants will experience both forms of stimulation, in separate sessions. Stimulation will be applied as a probe to understand the basic phenomenon of how brain processes support episodic memory.
Eligibility Criteria
You may qualify if:
- Ages 18 to 35 years old
- Fluent in English
- Free of major neurological or psychiatric illness
- Right-handed
- Normal or corrected to normal vision
You may not qualify if:
- History of a psychiatric illness within the past two years
- History of a learning disorder (e.g., attention deficit disorder, dyslexia)
- History of neurological disorder or brain injury, including family history of epilepsy, convulsions or seizures, stroke; vascular, traumatic, tumoral, infectious, or metabolic lesion of the brain, even without a history of seizure, and without anticonvulsant medication, and any unexplained lifetime loss of consciousness/syncope
- Use of medications that reduce seizure threshold (e.g., tricyclic antidepressants, neuroleptic agents)
- History of neurosurgery
- History of heart disease
- Recreational drug use in the past two months
- Uncontrollable shaking, or inability to sit/lie still for one hour
- Evidence of neurological disorders or structural abnormalities, based on MRI
- Pregnancy
- Prior surgeries, conditions, and/or implants that are not MRI-safe, including: pacemaker, pacemaker wires, artificial heart valve, brain aneurysm surgery, middle ear implant, non-removable hearing aids, braces, or extensive dental work, implanted mechanical or electrical device, artificial limb or joint
- Foreign metallic objects in the body, such as bullets, BBs, shrapnel, or metalwork fragments
- History of metal work or ocular metallic foreign bodies
- History of uncontrolled migraines or susceptibility to headaches
- Use of centrally-acting medications and drugs, with the exception of caffeine, within the last 12 hours
- +5 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Boston Collegelead
Study Sites (1)
Boston College
Chestnut Hill, Massachusetts, 02467, United States
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 29, 2022
First Posted
May 16, 2022
Study Start
October 6, 2023
Primary Completion
December 31, 2025
Study Completion
December 31, 2025
Last Updated
February 25, 2026
Record last verified: 2026-02