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RECRUITINGINTERVENTIONAL

Intracranial Neurophysiological Signatures of Fear and Anxiety in Humans

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

About This Trial

Anxiety disorders such as post-traumatic stress disorder (PTSD) and generalized anxiety disorder (GAD) affect a large number of individuals with a significant portion of patients failing to improve with current treatments. The purpose of this study is to understand the brain mechanisms that produce fear and anxiety in humans. To accomplish this goal, we will measure the brain activity along with the heart rate and skin perspiration of patients while they are completing tasks on a computer. Some of the tasks will also use a virtual reality headset and transport the patient in a video game-like environment. These tasks will expose the participants to various levels of fear-provoking images. Participants with responsive neurostimulation (RNS) implants will be enrolled under Pro00117931 at Duke, but their results for fear and anxiety tasks will be reported under NCT05120635.

Who May Be Eligible (Plain English)

Who May Qualify: - 18 years of age or older - Has undergone acute depth or chronic responsive neurostimulation (RNS) electrode placement - Willing to provide willing to sign a consent form and participate in the study - Ability to read and write English fluently Who Should NOT Join This Trial: - Unwilling to provide willing to sign a consent form - Has not undergone acute depth or chronic responsive neurostimulation (RNS) electrode placement - Pregnant women - Participants with active psychosis - Participants with suicidal ideation - Participants with substance abuse issues Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * 18 years of age or older * Has undergone acute depth or chronic responsive neurostimulation (RNS) electrode placement * Willing to provide informed consent and participate in the study * Ability to read and write English fluently Exclusion Criteria: * Unwilling to provide informed consent * Has not undergone acute depth or chronic responsive neurostimulation (RNS) electrode placement * Pregnant women * Participants with active psychosis * Participants with suicidal ideation * Participants with substance abuse issues

Treatments Being Tested

DEVICE

Deep Brain Stimulation

Deep brain stimulation will be used

BEHAVIORAL

Virtual and augmented reality tasks

Virtual and augmented reality tasks will be used.

Locations (2)

University of California Los Angeles
Los Angeles, California, United States
Duke University Health System
Durham, North Carolina, United States