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PTSD - Post Traumatic Stress DisorderASCENTNCT07707102

Advancing Skills Through Consultation, Education, and Novel Technologies

A study testing Live workshop, AI-enhanced Web-based training and Consultation video calls in people with PTSD - Post Traumatic Stress Disorder, run by The University of Texas Health Science Center at San Antonio at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

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). Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
Conditions the study is for
PTSD - Post Traumatic Stress Disorder
What is being tested?
Live workshop, AI-enhanced Web-based training and Consultation video calls
Could I receive a placebo?
No, everyone receives an active treatment
How many people
300 participants
Where
1 siteUnited States
Study dates
20 Aug 2026to 31 Aug 2028
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

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

Who cannot join

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

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Stefanie Losavio, PhD contact

(210) 562-6714

ASCENT@uthscsa.edu

United States1 site, 1 recruiting
  • University of Texas Health Science Center at San Antonio

    San Antonio, Texas, 78229

    Stefanie LoSavio, PhD, 210-562-6714, losavio@uthscsa.edu

    Recruiting

Other trials in United States

About this study

Official title: Increasing the Reach of Evidence-Based PTSD Treatment: Development and Clinical Trial of Artificial Intelligence (AI)-Facilitated, Web-Based Written Exposure Therapy Training

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.

Read the detailed description

This study will enroll behavioral health providers (i.e., professional therapists) and test a training program for Written Exposure Therapy that includes

  1. an enhanced, web-based foundational training (web-based training plus integrated TherapyTrainer components) and
  2. an AI training support tool for competency development (TherapyTrainer).

This randomized clinical trial will compare web/AI training, among providers who serve Veterans and Service Members, to standard Written Exposure Therapy training (i.e., human-delivered live workshop and consultation calls) on provider, patient, and cost-effectiveness outcomes. There is no cross-over of conditions. Providers in both conditions will be eligible to earn continuing education credits and approval as Written Exposure Therapy Providers who have completed competency based training and two training cases.

Being tested
Live workshop, AI-enhanced Web-based training, Consultation video calls, TherapyTrainer
Keywords
Written Exposure Therapy, AI-facilitated training
Medical subject headings
Combat Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Live workshopBehavioural

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

  • AI-enhanced Web-based trainingBehavioural

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

  • Consultation video callsBehavioural

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

  • TherapyTrainerBehavioural

    Also called AI Training Tool

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

Study groups in NCT07707102
Study groupRoleWhat they receive
Workshop + Consultation CallsActive comparator10-hour, live workshop over 2 days with a live trainer via video conferencing. There will also be twelve 1 hour calls with a live therapy consultant .
Receives: Behavioral: Live workshop; Behavioral: Consultation video calls
Workshop + TherapyTrainerActive comparator10-hour, live workshop over 2 days with a live trainer via video conferencing.There will also be approximately 12 hours of engagement with the AI training support tool (TherapyTrainer)
Receives: Behavioral: Live workshop; Behavioral: TherapyTrainer
Web-Based Training + Consultation CallsActive comparatorAI enhanced Web-based training with no live meetings, but approximately 8-10 hours of asynchronous, self-paced training. There will also be twelve 1 hour calls with a live therapy consultant .
Receives: Behavioral: AI-enhanced Web-based training; Behavioral: Consultation video calls
Web-based Training + TherapyTrainerActive comparatorAI enhanced Web-based training with no live meetings, but approximately 8-10 hours of asynchronous, self-paced training. There will also be approximately 12 hours of engagement with the AI training support tool (TherapyTrainer)
Receives: Behavioral: AI-enhanced Web-based training; Behavioral: TherapyTrainer

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Provider WET Competency

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

    Measured: Baseline to 7 months

Secondary outcomes (2)
  1. Completion of Practice Cases

    Number of participants that complete practice cases

    Measured: 4 months

  2. Time to complete Practice Cases

    Number of days to complete two training cases (real or simulated)

    Measured: 4 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Jul 2026
  2. Study start20 Aug 2026
  3. Primary completion31 Aug 2028 (estimated)
  4. Study completion31 Aug 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Model description
Three hundred providers will be randomized at a 1:1 ratio to a foundational learning condition and a competency development condition (2 x 2 design).
Masking
None (open label)
Enrolment
300 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07707102
Sponsor's protocol ID
STUDY00002482
Other IDs
HT9425-25-1-0585
Acronym
ASCENT
Status last verified
Aug 2026
First submitted
10 Jul 2026
Last updated
24 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: The PI will ensure all mechanisms used to share data will include proper plans and safeguards for the protection of privacy, confidentiality, and security for data dissemination and reuse (e.g., all data will be de-identified and will not be traceable to a specific study participant).

Questions about this trial

What is this clinical trial studying?

A study testing Live workshop, AI-enhanced Web-based training and Consultation video calls in people with PTSD - Post Traumatic Stress Disorder, run by The University of Texas Health Science Center at San Antonio at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 24 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Stefanie Losavio, PhD ((210) 562-6714, ASCENT@uthscsa.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Provider WET Competency (time frame: Baseline to 7 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Aug 2026.

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