Fear Conditioning Using Computer-Generated Virtual Reality
2 other identifiers
observational
202
1 country
1
Brief Summary
The purpose of this study is to use a computer-generated virtual reality environment to study fear conditioning. Fear conditioning is used to explore the causes and persistence of anxiety and anxiety disorders. When confronted with fearful or unpleasant events, people can develop fear of specific cues that were associated with these events as well as to the environmental context in which the events occurred via a process called classical or aversive conditioning. Advances in computer-generated visual stimulations could facilitate the design of new aversive conditioning studies. This study will develop a virtual reality environment to examine human contextual fear conditioning in the laboratory. During the procedure, moderately painful stimuli will be administered. Participants in this study will be screened with a medical history, physical examination, psychiatric evaluation, and hearing test. Participants will wear headphones and special goggles that will enable them to view a virtual reality environment. Measures will be taken during the study to see how the brain adapts to environmental stimuli.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2001
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 22, 2001
CompletedFirst Submitted
Initial submission to the registry
October 26, 2001
CompletedFirst Posted
Study publicly available on registry
October 29, 2001
CompletedStudy Completion
Last participant's last visit for all outcomes
April 10, 2012
CompletedJuly 2, 2017
April 10, 2012
October 26, 2001
June 30, 2017
Conditions
Keywords
Eligibility Criteria
You may qualify if:
- Subjects will be healthy volunteers ages 7-50 recruited through advertisements in the local media.
- Subjects will be free of current or past psychotic disorder and organic central nervous system disorders.
- All children will be screened for lifetime history of psychiatric disorders using the K-SADS Interview. The interview will be administered by a trained clinician (at least master level) supervised by Dr. Pine.
- The children/adolescents will be able to give assent and parents will give consent.
- They will have an IQ greater than 70 based on WASI.
You may not qualify if:
- Ongoing medical illness that could interfere with the study
- Current psychiatric or neurological disorder (including seizure)
- Past psychotic disorder
- Current substance abuse
- Current psychotropic medication
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Institutes of Health Clinical Center, 9000 Rockville Pike
Bethesda, Maryland, 20892, United States
Related Publications (3)
Grillon C, Davis M. Fear-potentiated startle conditioning in humans: explicit and contextual cue conditioning following paired versus unpaired training. Psychophysiology. 1997 Jul;34(4):451-8. doi: 10.1111/j.1469-8986.1997.tb02389.x.
PMID: 9260498BACKGROUNDGrillon C, Ameli R, Woods SW, Merikangas K, Davis M. Fear-potentiated startle in humans: effects of anticipatory anxiety on the acoustic blink reflex. Psychophysiology. 1991 Sep;28(5):588-95. doi: 10.1111/j.1469-8986.1991.tb01999.x.
PMID: 1758934BACKGROUNDGrillon C, Ameli R, Goddard A, Woods SW, Davis M. Baseline and fear-potentiated startle in panic disorder patients. Biol Psychiatry. 1994 Apr 1;35(7):431-9. doi: 10.1016/0006-3223(94)90040-x.
PMID: 8018793BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Thomas C Quinn, M.D.
National Institute of Allergy and Infectious Diseases (NIAID)
Study Design
- Study Type
- observational
- Sponsor Type
- NIH
Study Record Dates
First Submitted
October 26, 2001
First Posted
October 29, 2001
Study Start
October 22, 2001
Study Completion
April 10, 2012
Last Updated
July 2, 2017
Record last verified: 2012-04-10