Fear and Avoidance in PTSD Patients
NCT04770584 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 300
Last updated 2026-05-05
Summary
The purpose of this research study is to study how the brain learns to avoid certain stimuli or situations using an experimental paradigm. The big goal is to measure brain responses and subject's feelings and expectations when they are learning to actively avoid experimental stimuli, and how fear extinction learning and monetary cost can change how and when subjects are to avoid.
Conditions
- Post Traumatic Stress Disorder
Interventions
- BEHAVIORAL
-
Fear Conditioning
Participants will be administered increasing intensities of mild electric shock via electrodes connected to the foot. New Biopac stimulators that can deliver higher shock intensity, provided participants agreement will be used to assure adequate conditioning levels. Stimulation is measures in milliamps (mA), and each delivered stimulation will be 0.5 seconds long (500 milliseconds). To colored (blue, red, \& yellow) light stimuli (CS). The light stimulus is followed by a shock or no shock depending on color.
- OTHER
-
Avoidance conditioning
Via button pressing. Only one stimulus-CS will enable control over experiencing the shock: the participant can press the button during the first 2 seconds of the light presentation to avoid the shock.
- OTHER
-
Pavlovian fear extinction learning
After avoidance conditioning, the CS+ associated with avoidance responding appears with no button to press and no shock is administered.
- OTHER
-
Willingness to pay to avoid shock
On the next day, participants receive a monetary stipend to use to pay to guarantee that they are not to receive any shocks if they press a button from the CS+. This and all previously described experimental phases noted above will occur inside of the fMRI scanner.
Sponsors & Collaborators
-
National Institute of Mental Health (NIMH)
collaborator NIH -
The University of Texas Health Science Center, Houston
lead OTHER
Principal Investigators
-
Mohammed Milad, PhD · The University of Texas Health Science Center at Houston (UTHealth Houston)
Study Design
- Allocation
- NA
- Purpose
- BASIC_SCIENCE
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2021-09-09
- Primary Completion
- 2028-01-31
- Completion
- 2028-01-31
Countries
- United States
Study Locations
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