[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT07216222":3,"trial-entities:NCT07216222":77,"trial-summary:NCT07216222":83},{"id":4,"nct_id":4,"org_study_id":5,"brief_title":6,"official_title":7,"overall_status":8,"completion_date":9,"status_verified_date":10,"last_update_date":11,"start_date":12,"sponsor_name":13,"lead_sponsor_class":14,"has_dmc":15,"brief_summary":16,"detailed_description":17,"conditions":18,"keywords":22,"study_type":23,"primary_purpose":24,"phases":25,"enrollment_info":27,"interventions":30,"primary_outcomes":37,"secondary_outcomes":47,"sex":48,"minimum_age":49,"maximum_age":50,"healthy_volunteers":15,"eligibility_criteria":51,"std_ages":60,"locations":63,"central_contacts":73,"overall_officials":74,"references":75,"see_also_links":76},"NCT07216222","IRB-24-6010","K08 VR Fear Conditioning","Intracranial Recording and Stimulation of the Human Hippocampal-Amygdala Circuit During Virtual Reality Fear Conditioning","ENROLLING_BY_INVITATION","2030-02-28","2025-10","2025-10-14","2025-03-01","University of California, Los Angeles","OTHER",true,"The goal of this clinical trial is to learn how people respond to fear-related experiences in a virtual reality (VR) environment. The study will also look at how brain activity and body responses are connected to learning and memory of fear. To do so, we recruit individuals who are already implanted with a Responsive Neurostimulator (RNS) device for the treatment of epilepsy. This research may help improve our understanding of anxiety disorders and how to better treat them in the future.\n\nThe main questions it aims to answer are: 1) How do people learn to associate certain cues in VR with feelings of fear or safety? 2) What brain and body responses happen during fear learning?\n\nParticipants will: 1) Wear a virtual reality headset and experience different environments and sounds, 2) Have their brain activity, heart rate, and sweating measured, and 3) Receive safe, mild electrical pulses through the RNS device during the study to help study fear learning. Participants will attend one or more study sessions, each lasting about 3-4 hours.",null,[19,20,21],"Anxiety and Fear","PTSD","Veteran",[],"INTERVENTIONAL","BASIC_SCIENCE",[26],"NA",{"count":28,"type":29},70,"ESTIMATED",[31],{"type":32,"name":33,"description":34,"armGroupLabels":35},"DEVICE","Deep Brain Stimulation","Deep brain stimulation via the Responsive Neurostimulator (RNS) device.",[36],"All RNS Participants",[38,42,45],{"measure":39,"description":40,"timeFrame":41},"Intracranial EEG activity","Power in the theta band (\\~3-12 Hz).","Baseline",{"measure":43,"description":44,"timeFrame":41},"Skin conductance activity","Electrodermal response during the fear conditioning experiment, as quantified by changes in electrical conductance between electrodes placed on the palm.",{"measure":46,"timeFrame":41},"Heart rate",[],"ALL","18 Years","70 Years",{"inclusion":52,"exclusion":58,"raw_text":59},[53,54,55,56,57],"Male","Female","Between 18 and 70 years of age","Adequate visual and auditory acuity to allow neuropsychological testing","Have undergone surgical placement of NeuroPace RNS System for the treatment of epilepsy or post-traumatic stress disorder",[],"Inclusion Criteria:\n\n* Male\n* Female\n* Between 18 and 70 years of age\n* Adequate visual and auditory acuity to allow neuropsychological testing\n* Have undergone surgical placement of NeuroPace RNS System for the treatment of epilepsy or post-traumatic stress disorder\n\nExclusion Criteria:\n\n\\- History of traumatic brain injury",[61,62],"ADULT","OLDER_ADULT",[64],{"facility":65,"city":66,"state":67,"zip":68,"country":69,"geoPoint":70},"UCLA Semel Institute for Neuroscience and Human Behavior","Los Angeles","California","90024","United States",{"lat":71,"lon":72},34.05223,-118.24368,[],[],[],[],{"nct_id":4,"conditions":78,"biomarkers":82},[79,80,81],"Anxiety Disorder","Post-Traumatic Stress Disorder","Seizure Disorder",[],{"nct_id":4,"found":84,"summary":17,"prompt_version":17},false]