Actively Recruiting
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
Eligibility Criteria
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)
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
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
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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