RECRUITING

Intracranial Neurophysiological Signatures of Fear and Anxiety in Humans

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Intracranial Neurophysiological Signatures of Fear and Anxiety in Humans

Quick Facts

Study Start:2021-10-01
Study Completion:2026-06-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05120635

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 70 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * 18 years of age or older
  2. * Has undergone acute depth or chronic responsive neurostimulation (RNS) electrode placement
  3. * Willing to provide informed consent and participate in the study
  4. * Ability to read and write English fluently
  1. * Unwilling to provide informed consent
  2. * Has not undergone acute depth or chronic responsive neurostimulation (RNS) electrode placement
  3. * Pregnant women
  4. * Participants with active psychosis
  5. * Participants with suicidal ideation
  6. * Participants with substance abuse issues

Contacts and Locations

Study Contact

Gabriela Vilchez
CONTACT
9196812577
suthanalab@duke.edu

Principal Investigator

Nanthia Suthana, PhD
PRINCIPAL_INVESTIGATOR
Duke Health

Study Locations (Sites)

University of California Los Angeles
Los Angeles, California, 90024
United States
Duke University Health System
Durham, North Carolina, 27705
United States

Collaborators and Investigators

Sponsor: Duke University

  • Nanthia Suthana, PhD, PRINCIPAL_INVESTIGATOR, Duke Health

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2021-10-01
Study Completion Date2026-06-30

Study Record Updates

Study Start Date2021-10-01
Study Completion Date2026-06-30

Terms related to this study

Additional Relevant MeSH Terms

  • Fear
  • GAD
  • Emotional Memory
  • PTSD