Houston, TXNCT04770584Now EnrollingIRB Ready

Post Traumatic Stress Disorder Clinical Trial in Houston, TX

Access cutting-edge post traumatic stress disorder treatment through this clinical trial at a research site in Houston. Study-provided care at no cost to qualified participants.

Sponsored by The University of Texas Health Science Center, Houston

Quick Self-Assessment

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Expert Care in Houston

Access post traumatic stress disorder specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related post traumatic stress disorder treatment provided free

Apply for This Houston Location

Check if you qualify for this post traumatic stress disorder clinical trial in Houston, TX

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Houston

    Convenient for TX residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Houston site if eligible
  4. 4Begin participation

About This Post Traumatic Stress Disorder Study in Houston

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.

Sponsor: The University of Texas Health Science Center, Houston

Who Can Participate

Inclusion Criteria

18 - 70 years of age
Female or Male
SCID diagnosis consistent with no current psychiatric disorders, and no current PTSD
History of trauma exposure
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)

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Houston?

Yes, this clinical trial (NCT04770584) has an active research site in Houston, TX that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Post Traumatic Stress Disorder Treatment Options in Houston, TX

If you're searching for post traumatic stress disorder treatment options in Houston, TX, this clinical trial (NCT04770584) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Houston research site is actively enrolling participants for this clinical trial. You'll receive care from experienced post traumatic stress disorder specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all post traumatic stress disorder clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Houston, TX