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Adaptive Decision-making And Personalized Treatment for PTSD (ADAPT-PTSD)

Adaptive Decision-making And Personalized Treatment for PTSD (ADAPT-PTSD)

Recruiting
18 years and older
All
Phase N/A

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Overview

By doing this research project, the investigators hope to learn which strategies work best to help veterans who are not benefiting from their first PTSD treatment or not completing between-session homework assignments regularly that might improve treatment response. The investigators also want to learn how best to match the right type and amount of treatment to each individual veteran. By conducting this research project, they hope to:

  • See if trying a different treatment strategy for veterans not responding to their first PTSD treatment would be more helpful
  • See if sending text message prompts between sessions encourages more completion of between-session homework

Description

This study is designed to assist the investigators in answering the clinical question of how to address non-response to first line PTSD treatments. Utilizing an innovative Hybrid Experimental Design (HED), the proposed study involves multiple, sequential randomizations to both therapist-delivered and digital interventions operating on short and long timescales to determine the optimal combination and sequencing of evidence-based interventions to maximize response. This will result in actionable data and, consistent with a personalized medicine approach, an implementable, adaptive treatment regimen that optimizes clinical resource allocation. By recruiting and providing treatment in routine care settings serving veterans with PTSD, the study design maximizes generalizability, relevance to the VA mission, and implementation potential.

Eligibility

Inclusion Criteria:

  1. Veterans eligible for PE and CPT at the participating PTSD treatment-providing clinic who are
  2. At least 18 years or older
  3. Score ≥ 31 on the PCL-5 secondary to a Criterion A traumatic event
  4. Own a mobile device that can be used for the therapy companion mobile app (Prolonged Exposure (PE) coach or Cognitive Processing Therapy (CPT) coach).

Exclusion Criteria:

  1. Acute suicide risk requiring clinical intervention
  2. Need for detoxification
  3. Unmanaged psychosis or bipolar disorder
  4. Severe cognitive impairment that makes it unlikely that participants can adhere to the study regimen (as evidenced by confusion, inability to track discussion or answer questions, or other clear and significant indicators of cognitive impairment)
  5. Current or past 12-month engagement in PE or CPT.

Study details
    Posttraumatic Stress Disorder
    PTSD

NCT07176273

The University of Texas Health Science Center at San Antonio

15 October 2025

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FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

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Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

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The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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