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

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Device, Behavioral, Diagnostic test
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 55
Healthy Volunteers: t
View:

• Age 18 years or older

• For Aims I and III: Diagnosis of focal epilepsy or temporal lobe lesion; patients undergoing evaluation for or having undergone epilepsy surgery

• For Aim II: Healthy adult participants

• Full-Scale IQ ≥ 70

• English proficiency sufficient to understand and complete the task

• For Aim I: Enrolled in or eligible for Emory University epilepsy surgery research registry

• For Aim III: Undergoing clinically indicated stereoelectroencephalography (SEEG) at UC Davis Medical Center

• Able to provide informed consent (or for Aim I retrospective component, prior consent in Emory registry)

Locations
United States
California
UC Davis Medical Center
RECRUITING
Sacramento
Georgia
Emory University Hospital
RECRUITING
Atlanta
Contact Information
Primary
Nigel P Pedersen, MD
nppedersen@health.ucdavis.edu
916-734-3251
Time Frame
Start Date: 2024-07-01
Estimated Completion Date: 2030-06-30
Participants
Target number of participants: 620
Treatments
Experimental: Aim I: Lesion-Symptom Mapping
Patients with temporal lobe lesions (n≈310) and healthy controls (n≈150) at Emory University. Retrospective cohort with existing surgical lesions plus prospectively enrolled new surgical patients (\~60 over 5 years).~Intervention(s): Behavioral: Virtual Tour Recognition Memory Task; Diagnostic: MRI neuroimaging and neuropsychological assessment
Experimental: Aim II: Scalp ERP Study
Healthy participants (n=80) recruited from UC Davis campus community. Intervention: Behavioral: Virtual Tour Recognition Memory Task (still-image version) during Scalp EEG/ERP recording and eye tracking
Experimental: Aim III: Intracranial EEG
Patients with epilepsy undergoing clinically indicated SEEG (n≈80) at UC Davis Medical Center.~Behavioral Intervention: Virtual Tour Recognition Memory Task; Other Intervention: Intracranial EEG recording via clinically placed electrodes, a minority of which have research microelectrodes (FDA-approved Dixi micro-macro or Behnke-Fried Ad-Tech electrodes)
Related Therapeutic Areas
Sponsors
Collaborators: Emory University
Leads: University of California, Davis

This content was sourced from clinicaltrials.gov