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NCT Number: NCT04770584

Fear and Avoidance in PTSD Patients

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.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

UTHealth Houston

Houston, Texas, 77054, United States

Location status: Recruiting

Location contact

Mohammed R. Milad, PhD

CONTACT

[email protected]

About this study

This study aims to study the neural correlates of avoidance learning using a recently validated conditioning and active avoidance paradigm (CAAP). The overarching objective is to measure the neural correlates of active avoidance, and how fear extinction learning and monetary cost modulate these avoidance responses. Participants will include healthy controls (HC), trauma-exposed healthy controls (TEHC), and participants with post-traumatic stress disorder (PTSD). Avoidance is common and often hinders the progression and success of extinction-based exposure therapy in PTSD. The data to be gathered in this study will enable us to probe neural mechanisms of avoidance, extinction, and decision-making to avoid or not, in addition to understanding the impact of cost on avoidance decision-making. These data will provide a more integrated platform for the understanding of the mechanisms of avoidance in both trauma-exposed healthy controls and PTSD psychopathology, which has important implications for treatment.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 - 70 years of age
  • Female or Male
  • Inclusion Criteria: PTSD Subjects

a. Diagnosis of current PTSD

  • Inclusion Criteria: Trauma-exposed healthy controls (TEHC)
  • SCID diagnosis consistent with no current psychiatric disorders, and no current PTSD
  • History of trauma exposure
  • Inclusion Criteria: Healthy controls (HC)
  • SCID diagnosis consistent with no current psychiatric disorders ("Axis I" disorders).
  • No history of trauma exposure
  • Willing and able to provide informed consent.

Exclusion criteria

for ALL subjects:

  • History of neurologic disease (e.g. tic disorder)
  • Current significant suicidal ideation, plan or intent or suicidal behavior in past 6 months based on CSSRS or Self-injurious behavior that involves suicidal intent, requires medical attention, or occurs daily
  • History of seizure or significant head trauma
  • History of the serious/significant psychiatric diagnosis ("Axis I" disorders)
  • Use of neuroleptics within one year prior to study
  • Current substance use (assessed by urine toxicology; positive urine toxicology screen for any substance, with the exception of THC). Per PI judgement and approval: if urine toxicology is positive for a substance, participant may be eligible to proceed with study provided their urine toxicology (or saliva test for THC) is negative at experimental visit(s)
  • Pregnancy (to be ruled out by urine ß-HCG)
  • Metallic implants or devices contraindicating magnetic resonance imaging
  • High risk of adverse emotional or behavioral reaction, and/or an inability to understand study procedures or the informed consent process

Additional exclusion criteria for Trauma-exposed healthy controls (TEHC) group and Healthy controls (HC) group:

  • Current psychiatric diagnosis ("Axis I" diagnoses)

Treatment and study plan

Fear Conditioning

Behavioral

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.

Avoidance conditioning

Other

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.

Pavlovian fear extinction learning

Other

After avoidance conditioning, the CS+ associated with avoidance responding appears with no button to press and no shock is administered.

Willingness to pay to avoid shock

Other

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.

Primary outcomes

  1. Skin Conductance Response (SCR)

    Time frame: Experimental Day 1, Experimental Day 2

    Skin Conductance Response (SCR) assesses the stress/seat level, or level of anxiety in a particular moment, or in response to a specific cue. SCR will be reported in microsiemens.

  2. Functional MRI (fMRI) responses

    Time frame: Experimental Day 1, Experimental Day 2

    fMRI data, including blood-oxygen-level-dependent (BOLD) responses, is used in neuroimaging studies assess neural correlate activations and observe the increase/decrease in activation of a particular brain area in response to a specific cue.

Study contacts

Contact information is provided by the study sponsor or research team.

Mohammed Milad, PhD

CONTACT

[email protected]

713-486-2754

Sponsors and collaborators

Lead sponsor

The University of Texas Health Science Center, Houston

Other

Collaborators

  • National Institute of Mental Health (NIMH)

Registry information

Official study title

Neural Correlates of Active Avoidance Learning and Their Interactions With Fear Extinction Mechanisms in PTSD Patients

Important dates

Study start
2021
Primary completion
2028
Study completion
2028
First posted
Feb 25, 2021
Registry last updated
May 5, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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