NCT07442266

Brief Summary

The goal of this clinical trial is to examine how repeated memory retrieval changes visual representations in the brain in healthy adult participants. Specifically, the study aims to determine whether repeated recall strengthens or transforms neural representations in visual cortex compared to a time-matched control condition. The main questions it aims to answer are: 1) Does repeated retrieval produce cumulative changes in visual cortical representations compared to a control condition matched for elapsed time? 2) Do these representational changes differ for simple spatial stimuli and complex natural images? Researchers will compare neural activity patterns during repeated retrieval to those during a control retrieval condition to determine whether repeated recall leads to systematic changes in representational structure beyond those attributable to the passage of time. Participants will: 1) complete two fMRI sessions. 2) Undergo a localizer session including anatomical imaging, population receptive field (pRF) mapping, and a visual category localizer task. 3) Study cue-stimulus pairs consisting of either simple spatial patterns or natural images. 4) Recall previously studied stimuli multiple times during repeated and control retrieval conditions while undergoing fMRI scanning. Brain activity patterns during study and recall will be compared to assess how repeated retrieval influences the structure and tuning of visual representations.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Feb 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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

Study Start

First participant enrolled

February 3, 2026

Completed
21 days until next milestone

First Submitted

Initial submission to the registry

February 24, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

March 2, 2026

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2026

Completed
Last Updated

March 2, 2026

Status Verified

February 1, 2026

Enrollment Period

6 months

First QC Date

February 24, 2026

Last Update Submit

February 27, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Representational Change in Visual Cortex

    Difference in multivoxel BOLD activity patterns in visual cortex between repeated and control retrieval conditions during fMRI.

    1 hour

Study Arms (1)

Experimental Memory Retrieval Task

EXPERIMENTAL

All participants will complete a visual memory encoding and retrieval task during fMRI scanning. The study uses a within-subject design in which each participant completes both a repeated retrieval condition and a time-matched control retrieval condition. This design allows comparison of neural representational changes associated with repeated retrieval while controlling for elapsed time.

Behavioral: Visual Memory Encoding and Retrieval Task During fMRI

Interventions

Participants will study cue-stimulus associations and subsequently retrieve the associated stimuli while undergoing fMRI scanning. Retrieval will occur under two conditions: (1) repeated retrieval, in which stimuli are recalled five times, and (2) control retrieval, in which stimuli are recalled twice with timing matched to the repeated condition. Neural activity patterns during study and recall will be measured using BOLD fMRI.

Experimental Memory Retrieval Task

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may not qualify if:

  • Under the age of 18 or over the age of 40
  • Does not live in the United States or is not a native speaker of English
  • Diagnosis of a neurological disorders, a history of head trauma, or diagnosis of psychiatric disorder
  • Imperfect and uncorrected visual acuity, color blindness, or imperfect hearing
  • Magnetically or mechanically activated implants or other untested metal implants
  • Claustrophobia

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Brown University Magnetic MRI Research Facility

Providence, Rhode Island, 02906, United States

RECRUITING

Central Study Contacts

Serra E Favila, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
SINGLE GROUP
Model Details: Within-subject experimental design in which all participants complete all conditions during fMRI.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 24, 2026

First Posted

March 2, 2026

Study Start

February 3, 2026

Primary Completion

August 1, 2026

Study Completion

August 1, 2026

Last Updated

March 2, 2026

Record last verified: 2026-02

Locations