ClinicalTrials.gg
Enrolling by invitationNCT05092100Updated Aug 31, 2026

Neural Mechanisms for Reducing Interference During Episodic Memory Formation

An interventional study of Visual stimulus similarity and fMRI in Behavior, sponsored by University of Oregon. Enrolling by invitation at 1 site in United States. Open to participants aged 18 Years to 80 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-31.

Sponsored by University of Oregon · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
2,900
Allocation
Non-randomized
Ages
18 Years to 80 Years
Sex
All
01

Study summary

Healthy individuals from the University of Oregon and surrounding community will be recruited for participation in behavioral, fMRI and eye tracking experiments that investigate human memory. Recruitment will involve emails, flyers, and local advertisements. Individuals between the ages of 18-80 (or 18-35 for some studies) will be eligible.

The broad objective of the research is to understand how humans form distinct memories for similar experiences. Experimental sessions will involve studying and trying to remember various images (e.g., images of natural scenes). The intervention will involve manipulating the similarity and/or learning protocol for the studied images. Outcome measures will include (a) behavioral measures of memory, and/or (b) fMRI measures of hemodynamic activity, and/or (c) eye tracking measures of gaze direction. Experimental sessions will last approximately 1-3 hours.

Read the detailed description

Objective: The goal of the research studies is to understand how memories are formed for similar experiences such that interference (confusion) between these memories is minimized. Of particular interest is the role of the hippocampus (a brain region important for memory).

Participants: Healthy individuals from the University of Oregon and surrounding community will be recruited through fliers, emails, and advertisements. For some of the studies, individuals between 18-80 years of age will be recruited. For others, individuals between 18-35 will be recruited.

Design: All studies will involve studying and trying to remember various images (e.g., natural scenes) displayed on a computer screen. Memory decisions will be made and recorded using a computer keyboard or external button box. The similarity of images and/or the specific learning procedures (e.g., number of repetitions, order of study, etc.) will be manipulated. Experimental sessions will be conducted in behavioral testing rooms (with or without eye tracking equipment) and/or in an MRI scanner.

Outcomes: Measures of interest will include (a) behavioral responses, (b) fMRI measures of hemodynamic responses, and/or (c) gaze direction as measured by eye tracking equipment. Behavioral responses will consist of simple memory decisions, such as indicating whether or not an image has been seen before or trying to remember associations between images. fMRI data will be analyzed using multivariate pattern similarity analyses. Eye tracking data will be used to measure the specific spatial locations of images that participants fixate on.

02

Conditions studied

  • Behavior

Browse trials for

Keywords

  • behavior, memory
03

In context

Behavior

1,573 studies on the registry are indexed under Behavior; 313 are open to participants now.

This study's planned enrollment of 2,900 is above the median of 120 across 1,197 interventional studies indexed under Behavior.

Browse Behavior studies →

Lead sponsor

University of Oregon is the lead sponsor of 75 studies on the registry; 18 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Participants in behavioral studies must be:

  • healthy and between the ages of 18-35 years old
  • native English speakers
  • right-handed.

Participants in fMRI studies must be:

  • healthy and between the ages of 18-80 years old
  • native English speakers
  • right-handed.

Exclusion criteria

Exclusion Criteria:

For behavioral studies:

- Potential participants will be informed that use of psychoactive drugs, mental health disorders, and chronic or temporary sleep deficits (an average of less than 6 hours of sleep over the past month or less than 4 hours of sleep the night prior to the experimental session) are reasons for exclusion because of the potential influence on cognitive functioning.

For fMRI studies:

  • For some sub-studies, individuals older than age 35 will be excluded because of potential differences in cognitive and brain function across age groups that are beyond the scope of the proposed studies.
  • Individuals will be informed that use of psychoactive drugs, mental health disorders, and chronic or temporary sleep deficits (an average of less than 6 hours of sleep over the past month or less than 4 hours of sleep the night prior to the experimental session) are reasons for exclusion because of the potential influence on cognitive functioning.
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
2,900 participants (estimated)

Study arms

  • Experimental
    Behavioral

    This arm will use behavioral procedures to test memory for different visual stimulus conditions.

    Behavioral: Visual stimulus similarity

  • Experimental
    fMRI pattern similarity

    This arm will use fMRI and behavioral methods to test memory for different visual stimulus conditions.

    Behavioral: Visual stimulus similarity · Other: fMRI

  • Experimental
    eye tracking

    This arm will use eye tracking and behavioral methods to test memory for different visual stimulus conditions.

    Behavioral: Visual stimulus similarity · Behavioral: Eye tracking

Interventions

  • BehavioralVisual stimulus similarity

    Visual stimulus similarity will be varied in order to test for effects on memory. Learning protocol (the order and frequency with which stimuli are learned) will also be varied.

    Also known as: Learning protocol

  • OtherfMRI

    fMRI will be used to measure patterns of BOLD activity during learning.

  • BehavioralEye tracking

    Eye tracking will be used to measure patterns of eye movements when viewing images.

06

What researchers measure

Primary outcomes

  1. Behavior

    Behavioral responses will be recorded by keyboard or external button boxes. These responses will be used to assess the accuracy with which participants remember individual images. Accuracy will be averaged across stimuli within each learning condition to obtain measures of mean memory accuracy (i.e., the percentage of stimuli that were successfully remembered) per condition and participant.

    Time frame: Data will be collected over a 5 year period. Results from sub-studies will be analyzed within 6 months of the conclusion of data collection.

  2. fMRI pattern similarity

    fMRI will be used to measure hemodynamic (BOLD) responses as participants study images. Pattern similarity analyses will be applied to the fMRI data. Pattern similarity will be indexed by the correlation (r) between patterns of BOLD activity. Pattern similarity will be computed for images within and across different learning conditions.

    Time frame: Data will be collected over a 5 year period. Results from sub-studies will be analyzed within 6 months of the conclusion of data collection.

  3. eye tracking

    Eye tracking equipment will be used to measure gaze direction and fixations as participants study images. These data will be used to calculate variables such as the number of saccades (eye movements) made and the percentage of time (within each trial) spent looking at each portion of an image. Data from individual trials will be averaged across trials within each learning condition. This will yield mean values per condition and participant.

    Time frame: Data will be collected over a 5 year period. Results from sub-studies will be analyzed within 6 months of the conclusion of data collection.

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Yes — de-identified fMRI data will be shared via a public repository

Supporting information: Study protocol, Analytic code

Time frame: Data will be made available approximately at the time of (or before) manuscript publication. At the latest, data will be made available 1 year after manuscript publication.

Access criteria: Data will be publicly accessible.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 31, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05092100
Lead sponsor
University of Oregon
Responsible party
Sponsor
First posted
Oct 25, 2021
Start date
Sep 29, 2021
Primary completion
Dec 2026 (estimated)
Completion
Jan 2027 (estimated)
Last update
Aug 31, 2026

Study contacts

Brice A Kuhl, Ph.D.
principal investigator · University of Oregon

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

No contact was published for this record. The registry link below has the sponsor’s details.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion