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Visual Stimuli and Brain Imaging for Memory Behavior

N/A
Waitlist Available
Led By Brice A Kuhl, Ph.D.
Research Sponsored by University of Oregon
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Must not have
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
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
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 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.
Awards & highlights
No Placebo-Only Group

Summary

This trial is recruiting healthy individuals from the University of Oregon and surrounding community to participate in behavioral, fMRI and eye tracking experiments that investigate human memory.

Who is the study for?
This trial is for healthy, right-handed native English speakers from the University of Oregon area. For behavioral studies, participants must be aged 18-35. For fMRI studies, they can be between 18-80 years old. People with mental health disorders, drug use or sleep deficits are excluded.
What is being tested?
The study investigates memory formation by having participants remember images while their brain activity and eye movements are tracked using fMRI and eye tracking technology. The similarity of images and learning methods will vary to see how it affects memory.
What are the potential side effects?
There may not be direct side effects from participating in this study since it involves non-invasive procedures like remembering images, fMRI scanning, and eye tracking which typically do not cause harm.

Eligibility Criteria

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
Select...
I am under 35, don't use psychoactive drugs, have no mental health disorders, and sleep well.
Select...
I don't use psychoactive drugs, have mental health disorders, or suffer from chronic sleep deficits.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~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.
This trial's timeline: 3 weeks for screening, Varies for treatment, and 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. for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Behavior
eye tracking
fMRI pattern similarity

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

3Treatment groups
Experimental Treatment
Group I: fMRI pattern similarityExperimental Treatment2 Interventions
This arm will use fMRI and behavioral methods to test memory for different visual stimulus conditions.
Group II: eye trackingExperimental Treatment2 Interventions
This arm will use eye tracking and behavioral methods to test memory for different visual stimulus conditions.
Group III: BehavioralExperimental Treatment1 Intervention
This arm will use behavioral procedures to test memory for different visual stimulus conditions.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Eye tracking
2023
N/A
~50

Find a Location

Who is running the clinical trial?

University of OregonLead Sponsor
85 Previous Clinical Trials
43,501 Total Patients Enrolled
Brice A Kuhl, Ph.D.Principal InvestigatorUniversity of Oregon

Media Library

fMRI Clinical Trial Eligibility Overview. Trial Name: NCT05092100 — N/A
Behavior Research Study Groups: eye tracking, Behavioral, fMRI pattern similarity
Behavior Clinical Trial 2023: fMRI Highlights & Side Effects. Trial Name: NCT05092100 — N/A
fMRI 2023 Treatment Timeline for Medical Study. Trial Name: NCT05092100 — N/A
~177 spots leftby Dec 2025