Actively Recruiting

Phase Not Applicable
Age: 18Years - 55Years
All Genders
Healthy Volunteers
ID07580183

Investigations of Spatial Recognition Memory to Improve Cognitive Outcomes in Epilepsy Surgery

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

620

Participants Needed

2

Research Sites

N/A

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

Researchers are studying how the brain recognizes and remembers spatial scenes in people with temporal lobe epilepsy and lesions in the temporal lobe. Standard memory tests often miss important memory problems these patients face, especially with spatial and scene memory. The study aims to better understand how different brain areas contribute to familiarity-based recognition and recall using a virtual tour task and brain recording techniques. The goal is to improve predicting and preventing memory problems after epilepsy surgery. The study includes three main parts: First, around 310 patients with temporal lobe lesions and 150 healthy controls at Emory University complete a virtual tour memory task along with brain scans and neuropsychological assessments. Second, 80 healthy adults at UC Davis perform a similar task while undergoing scalp EEG and eye tracking to study brain activity patterns. Third, about 80 epilepsy surgery patients at UC Davis with implanted brain electrodes complete the task during intracranial EEG monitoring to record detailed brain signals. The study uses FDA-approved research electrodes and MRI imaging. Participants undergo the virtual tour task where they view and recall spatial scenes, with assessments scheduled over weeks or during hospital stays. The study measures accuracy in scene recognition and recall, brain activity patterns related to memory, and lesion-location correlations. Additional tests include neuropsychological batteries and visual imagery questionnaires. Follow-up testing occurs up to one year after surgery for some. Overall, the study combines behavioral tests, brain imaging, and electrophysiology to reveal how memory circuits function in epilepsy.

CONDITIONS

Brief 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 undergone epilepsy surgery for Aims I and III
  • Healthy adult participants for Aim II
  • Full-Scale IQ of 70 or higher
  • Sufficient English proficiency to understand and complete the tasks
  • Enrollment in or eligibility for Emory University epilepsy surgery research registry for Aim I
  • Undergoing clinically indicated stereoelectroencephalography (SEEG) at UC Davis Medical Center for Aim III
  • Ability to provide informed consent (or prior consent in Emory registry for Aim I retrospective component)
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 specified by the study protocol

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Behavioral Assessment

Duration - Up to 8 weeks from enrollment

Participants complete the Virtual Tour Recognition Memory Task consisting of study and test phases to assess spatial scene familiarity and recall.

1 to 2 visits depending on study arm

Intracranial EEG Monitoring

Duration - Typically 1 to 2 weeks hospital stay

Patients undergoing intracranial EEG with clinically placed electrodes, some including FDA-approved research electrodes, are monitored during the Virtual Tour task and resting state recordings.

Continuous monitoring during hospital stay

MRI Neuroimaging and Neuropsychological Assessment

Duration - Pre-surgery plus 6 months and 1 year post-surgery assessments

Participants undergo pre- and post-surgical MRI scans and extensive neuropsychological testing to assess cognitive function related to epilepsy surgery.

3 visits: pre-surgery, 6 months post-surgery, and 1 year post-surgery

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

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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