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NCT Number: NCT07617506

Neural Basis of Human Working Memory

This ClinicalTrials.gov entry corresponds to the Neural Basis of Human Working Memory protocol approved under Vanderbilt University Medical Center IRB #251231.

This study investigates the neural activity underlying human working memory, via local field potential changes (macro level) and/or single neuronal spiking changes (micro level) from depth electrodes placed for invasive seizure monitoring. Subjects will complete neurocognitive tasks while neural recordings are collected. Some patients will complete neurocognitive tasks while stimulation is applied via depth electrodes. Further understanding the neural activity changes underlying normal and impaired working memory may help to identify novel diagnostic methods and treatments for impaired working memory and may support the use of stimulation for treatment of memory disorders.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Undergoing SEEG monitoring at Vanderbilt University Medical Center
  • Age >18
  • English speaking

Exclusion criteria

  • Age <18
  • Not able to complete questionnaires (unable to comprehend instructions or follow directions)

Treatment and study plan

Primary outcomes

  1. Local field potential changes in response to working memory tasks

    Time frame: During patient's epilepsy monitoring stay, approximately 20-30 minutes

    Local field potential changes are from intracranial neural recordings taken while patients complete spatial working memory tasks. In the manual remember 1 remember 2 task, patients are instructed to hold down a cursor on a central location box colored one color or another on screen, while two boxes in locations sequentially flash on screen. Depending on the central location box color, the patient will drag their cursor to the first or second location box shown, after the central box has disappeared from screen. In the retro remember 1 remember 2 task, the color of the central box color is not shown until both location boxes have flashed onscreen. In the manual version, the central location box color is constant throughout the trial.

  2. Single unit neuronal spiking changes in response to memory tasks

    Time frame: During patient's epilepsy monitoring stay, approximately 20-30 minutes

    Single neuron spiking activity is recorded through SEEG micro neural recordings while patients complete working memory tasks.

  3. Behavioral performance changes with simulation

    Time frame: During patient's epilepsy monitoring stay, approximately 20-30 minutes

    Bipolar stimulation through pre-selected SEEG electrodes in the prefrontal cortex and surrounding areas will occur during the remember 1 remember 2 working memory tasks. Stimulation will be performed via the Ripple Neuromed Summit system. Stimulation will be tested with each patient prior to task to determine safety and tolerability, while patient is monitored by a neurosurgeon or neurologist.

Study contacts

Contact information is provided by the study sponsor or research team.

Christos Constantinidis, PhD

CONTACT

[email protected]

+1 (615) 936-2020

Lucas Chang, BS

CONTACT

[email protected]

615-421-3046

Sponsors and collaborators

Lead sponsor

Vanderbilt University Medical Center

Other

Collaborators

  • National Institute of Mental Health (NIMH)

Registry information

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Jun 1, 2026
Registry last updated
Jun 11, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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