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NCT07707102 · The University of Texas Health Science Center at San Antonio

Advancing Skills Through Consultation, Education, and Novel Technologies

(ASCENT)

What this study is about

This research study tests strategies to train behavioral health providers in Written Exposure Therapy (WET), an evidence-based treatment for posttraumatic stress disorder (PTSD). There are a number of evidence-based treatments for posttraumatic stress disorder (PTSD).

View original scientific description

This research study tests strategies to train behavioral health providers in Written Exposure Therapy (WET), an evidence-based treatment for posttraumatic stress disorder (PTSD). There are a number of evidence-based treatments for posttraumatic stress disorder (PTSD). However, most behavioral health providers have not received training in these PTSD treatments and do not offer them regularly to their patients. The researchers hope to learn about the optimal way to train behavioral providers in this type of treatment. This study is designed to determine the comparative effectiveness of different training strategies on key outcomes such as how much competency providers develop in the therapy and to how many patients they deliver the therapy. This study will help the researchers understand if we can help more providers learn to competently delivery Written Exposure Therapy by using strategies that are more convenient and cost less money, including web-based and AI-facilitated training supports. This study will also help us learn which training strategies work best for which providers so that in the future we can make personalized training recommendations.

Interventions

BEHAVIORAL

Live workshop

Approximately 10 hours (excluding breaks) over 2 days with a live trainer via video conferencing (e.g., Zoom)

BEHAVIORAL

AI-enhanced Web-based training

No live meetings, but approximately 8-10 hours of asynchronous training at the learner's pace over about 1 month.

BEHAVIORAL

Consultation video calls

Twelve 1-hour calls with a live therapy consultant via videoconferencing (e.g., Zoom)

BEHAVIORAL

TherapyTrainer

No live meetings, but approximately 12 hours of engaging with the AI training support tool (TherapyTrainer)

Primary outcome measures

Provider WET Competency

Time frame: Baseline to 7 months

A 20-item multiple choice treatment knowledge assessment. Higher scores indicate greater knowledge of WET.

Who can participate

This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.

Inclusion criteria

  • mental health provider;
  • serves veterans and/or service members with PTSD (by self-report);
  • willing to participate in either live or web-based training.

Exclusion criteria

  • 1\. has already completed formal training in Written Exposure Therapy

Where

  • San Antonio, Texas

Collaborators

Stanford University, Medical University of South Carolina, Boston University, Rush University Medical Center

Related conditions & keywords

PTSD - Post Traumatic Stress DisorderWritten Exposure TherapyAI-facilitated training

Frequently asked questions

What is a clinical trial?

A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.

Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.

Will I be compensated?

Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.

Will I receive a placebo instead of treatment?

When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.

Can I leave a trial if I change my mind?

Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.

How long does a clinical trial last?

Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.

Data: ClinicalTrials.gov · synced Aug 24, 2026 · Source of record for eligibility and locations

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1 of 300 participants interested
0% interest

See if this study fits

A short prescreen based on this study's listed criteria. A coordinator confirms eligibility — this is not a medical assessment.

Preparing your pre-screening questions…

Study locations

Choose your preferred location, or select flexible during enrollment.

RECRUITING

San Antonio

Texas

Location available

Express your interest

Share your contact details and a study coordinator can follow up about screening.

Secure & Confidential

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

What participation can include

  • Study-related care provided by the research team
  • Close monitoring by medical professionals
  • Possible compensation for time and travel*
  • The option to withdraw at any time
  • Contributing to medical research that may help future patients

*Compensation varies by study. Confirm details with coordinator.

Typical next steps

  1. 1.Submit this form
  2. 2.Phone screening
  3. 3.In-person assessment if eligible
  4. 4.Begin participation

Find More PTSD Trials by City

Browse all ptsd clinical trials in these cities — not just this study.

Looking for PTSD - Post Traumatic Stress Disorder Treatment in San Antonio?

Join others in Texas exploring innovative treatment options through clinical research

PTSD - Post Traumatic Stress Disorder Treatment Options in San Antonio, Texas

If you're searching for PTSD - Post Traumatic Stress Disorder treatment in San Antonio, participating in a clinical research study may provide access to innovative approaches under expert medical supervision. This study is actively recruiting participants in San Antonio and surrounding areas.

Clinical trials offer participants the opportunity to receive cutting-edge treatments while contributing to medical research that may help future patients with PTSD - Post Traumatic Stress Disorder. All study-related care is provided at no cost to participants.

Local Sites
1 locations in Texas
Now Enrolling
Up to 300 participants
Quick Start
Screening available now

Why Consider a Clinical Trial for PTSD - Post Traumatic Stress Disorder?

Potential Benefits

  • Access to new treatment approaches before public availability
  • Close monitoring by experienced medical professionals
  • Study-related care provided at no cost
  • Contribute to medical research for PTSD - Post Traumatic Stress Disorder

What to Expect

  • Initial screening to determine eligibility
  • Regular check-ups and monitoring visits
  • Possible compensation for time and travel
  • You can withdraw at any time

Frequently Asked Questions About This PTSD - Post Traumatic Stress Disorder Study

Important Clinical Trial Information

This information is provided for educational purposes and does not constitute medical advice. Clinical trial participation involves potential risks and benefits. Eligibility requirements apply and will be assessed during the screening process.

Study identifier: NCT07707102. For complete study details, visit ClinicalTrials.gov. Always consult with your healthcare provider before making decisions about your medical care or participating in clinical research.