Actively Recruiting

Phase Not Applicable
Age: 13Years - 25Years
All Genders
Healthy Volunteers
NCT07199907

Hippocampal and Frontoparietal Development and Inference

Led by University of Texas at Austin · Updated on 2025-09-30

142

Participants Needed

1

Research Sites

231 weeks

Total Duration

On this page

Sponsors

U

University of Texas at Austin

Lead Sponsor

N

National Institute of Mental Health (NIMH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to test if an intervention used to manipulate memory and inference can improve our understanding of how brain development supports these abilities in healthy adolescent and adult volunteers. The main questions it aims to answer are: (1) Do hippocampus and ventromedial prefrontal cortex shift from forming simple memories for singular experiences to more complex memories that link numerous experiences together?; (2) Does an improved ability to retrieve prior memories in parietal cortex during new learning have consequences for how those memories are organized at different ages?; and (3) Does the emerging memory control supported by ventromedial prefrontal cortex development facilitate the formation of optimally-organized memory representations? Adolescent participants (13-18 years) will perform two experimental tasks during functional magnetic resonance imaging (fMRI) scanning at three timepoints (T1-T3), spaced 1.5 years apart. Researchers will compare behavioral and neuroimaging data to a separate group of adults (19-25 years) who will perform the task at a single timepoint (T1). The tasks and comparison groups will allow us to isolate the neural processes that support memory and inference behavior, and how these processes change with age.

CONDITIONS

Official Title

Hippocampal and Frontoparietal Development and Inference

Who Can Participate

Age: 13Years - 25Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Right-handed
  • Normal or corrected to normal vision
  • Normal hearing
  • No contraindications for MRI
  • No history of neurological or psychiatric disorders at initial intake
  • Normal intelligence
  • Native or fluent English speaker
Not Eligible

You will not qualify if you...

  • Major medical illness or neurological disorder, including significant head trauma (loss of consciousness > 5 minutes)
  • Current or past psychiatric disorder or prior psychiatric hospitalizations
  • Intelligence scores more than 1 standard deviation below the mean on the WASI-II
  • History of special education placement
  • Non-native English speaker
  • Prior use of psychotropic medication (except antidepressants) longer than 1 month
  • History of moderate to severe cannabis use disorder
  • MRI exclusions such as claustrophobia, tattoos above the shoulders, permanent eyeliner, permanent retainer or spacer, artificial eyebrows, cardiac pacemaker, metal fragments in eye or body, heart valve replacement, brain clips, various prosthetic devices, metal implants, or suspected pregnancy

AI-Screening

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Trial Site Locations

Total: 1 location

1

The University of Texas at Austin

Austin, Texas, United States, 78712

Actively Recruiting

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Research Team

A

Alison R Preston, PhD

CONTACT

N

Nicole L Varga, Ph.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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