Actively Recruiting

Phase Not Applicable
Age: 18Years - 55Years
All Genders
Healthy Volunteers
NCT07580183

Spatial Scene Recognition Memory in Epilepsy Surgery

Led by University of California, Davis · Updated on 2026-05-12

620

Participants Needed

2

Research Sites

312 weeks

Total Duration

On this page

Sponsors

U

University of California, Davis

Lead Sponsor

E

Emory University

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study investigates the anatomical and physiological basis of spatial scene recognition memory in patients with temporal lobe epilepsy and temporal lobe lesions. Standard neuropsychological tests are insensitive to important memory deficits experienced by patients, particularly in spatial/scene memory, recollective experience, and familiarity processing. Using a validated virtual tour paradigm, the study examines how familiarity-based recognition and recall of spatial scenes relate to specific brain structures. In Aim I, a large cohort of patients with varied temporal lobe lesions at Emory University undergoes the virtual tour task with voxel-based lesion-symptom mapping to localize necessary brain regions. In Aim II, scalp event-related potentials and eye tracking in healthy participants at UC Davis characterize the temporal dynamics and lateralization of scene recognition. In Aim III, intracranial EEG recordings (including local field potentials and single-unit activity) in epilepsy surgery patients at UC Davis determine the precise network dynamics underlying spatial scene familiarity and recall. The long-term goal is to improve the prediction and prevention of cognitive morbidity from epilepsy surgery by providing a more complete model of spatial recognition memory circuits.

CONDITIONS

Official Title

Spatial Scene Recognition Memory in Epilepsy Surgery

Who Can Participate

Age: 18Years - 55Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Diagnosis of focal epilepsy or temporal lobe lesion for Aims I and III; patients undergoing evaluation for or having had epilepsy surgery
  • Healthy adult participants for Aim II
  • Full-Scale IQ of 70 or higher
  • Sufficient English proficiency to understand and complete tasks
  • Enrolled in or eligible for Emory University epilepsy surgery research registry for Aim I
  • Undergoing clinically indicated stereoelectroencephalography (SEEG) at UC Davis Medical Center for Aim III
  • Able to provide informed consent (or prior consent for Aim I retrospective participants)
Not Eligible

You will not qualify if you...

  • Full-Scale IQ below 70
  • Inability to provide informed consent
  • Age over 55 years for Aim III
  • History of neurological or psychiatric disorder for Aim II as per protocol

AI-Screening

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Trial Site Locations

Total: 2 locations

1

UC Davis Medical Center

Sacramento, California, United States, 95817

Actively Recruiting

2

Emory University Hospital

Atlanta, Georgia, United States, 30322

Actively Recruiting

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Research Team

N

Nigel P Pedersen, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

3

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