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RECRUITINGINTERVENTIONAL

Novel Multimodal Neural, Physiological, and Behavioral Sensing and Machine Learning for Mental States

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

In this program, the investigators will develop novel multimodal neural-behavioral-physiological monitoring tools (software and hardware), and machine learning models for mental states within social processes and beyond. The tools consist of a multimodal skin-like wearable sensor for physiological and biochemical sensing; a conversational virtual human platform to evoke naturalistic social processes; audiovisual affect recognition software; synchronization tools; and machine learning methods to model the multimodal data. The investigators will demonstrate the tools in healthy subjects without neural recordings and in patients with drug-resistant epilepsy who already have intracranial EEG (iEEG) electrodes implanted based on clinical criteria for standard monitoring to localize seizures, which is unrelated to our study.

Who May Be Eligible (Plain English)

For the healthy population, all subjects over the age of 18 who are able and willing to give willing to sign a consent form will be eligible. For the epilepsy population, inclusion criteria are: - Patients who suffer from drug-resistant epilepsy and already have intracranial EEG (iEEG) electrodes implanted based on clinical criteria for their standard seizure localization (unrelated to our study) will be eligible. Most patients are healthy adults outside of their epilepsy. - Subjects \>= 18 are only included in this study. - All patients with the above conditions and with already-implanted electrodes who are willing to participate and able to cooperate and follow research instructions will be recruited. Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
For the healthy population, all subjects over the age of 18 who are able and willing to give informed consent will be eligible. For the epilepsy population, inclusion criteria are: * Patients who suffer from drug-resistant epilepsy and already have intracranial EEG (iEEG) electrodes implanted based on clinical criteria for their standard seizure localization (unrelated to our study) will be eligible. Most patients are healthy adults outside of their epilepsy. * Subjects \>= 18 are only included in this study. * All patients with the above conditions and with already-implanted electrodes who are willing to participate and able to cooperate and follow research instructions will be recruited.

Treatments Being Tested

BEHAVIORAL

Virtual human social interaction

The participants will perform a social interaction with the virtual human agent platform to assess mental states.

BEHAVIORAL

Cold pressor test

Healthy participants will immerse one hand in cold water for less than 3 minutes, while physiological data will be collected by the new wearable sensor from the other hand.

Locations (2)

Rancho Los Amigos National Rehabilitation Center
Downey, California, United States
University of Southern California
Los Angeles, California, United States