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Advanced Wireless Augmented Reality-Enhanced Exposure Therapy for Posttraumatic Stress Disorder

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Secondary endpoints: 23 to 24v8
  2. Secondary endpoints: details revised at 8 of 23 entriesv7
  3. Secondary endpoints: details revised at 8 of 23 entriesv6
  4. Trial status: Not Yet Recruiting to Recruitingv5 Show 6 more changesShow less
    • Primary endpoints revised (9)
    • Study sites: 0 to 1
    • Start date changed from estimate of Aug 15, 2025 to Sep 1, 2025
    • Interventions: Traditional Exposure Therapy (ET) Treatment (Behavioral), Traditional Exposure Therapy (ET) Treatment with addition of Augmented Reality… to Stepwise Augmented Reality (AR) Component with Traditional Exposure Treatment for Nonresponders (Behavioral), Traditional Exposure Therapy…
    • Secondary endpoints: 15 to 23
    • Study description expanded, about 124 words
  5. Primary endpoints revised (9)
    • Secondary endpoints: 12 to 15
    • Study description revised
    v4
Show 2 earlier versionsHide 2 earlier versions
  1. Start date: Jun 1, 2025 to Aug 15, 2025v3
  2. Interventions: ARET + Traditional ET Treatment (Behavioral), Traditional ET Treatment (Behavioral) to Traditional Exposure Therapy (ET) Treatment (Behavioral), Traditional Exposure Therapy (ET) Treatment with addition of Augmented Reality…
    • Collaborators revised (2)
    • Study description expanded, about 2 words
    v2
  1. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Wayne State University
48 trials monitored
See 1 trial at risk
PTSD
889 trials monitored
See 54 trials at risk
The goal of this trial is to test how augmented reality exposure therapy (ARET) may potentiate the effects of traditional exposure therapy administered to U.S. military personnel diagnosed with PTSD. 40 adult males and females over the age of 18 that have served, or are currently serving, in the U.S. military, with a current diagnosis of PTSD, will be recruited. Participants will be randomized into two groups: 20 participants will receive ARET + traditional ET, with the remaining 20 to receive traditional ET only. The main questions this trial aims to answer are: * what are the different clinical and psychosocial functioning outcomes between veterans/active-duty personnel with PTSD who receive ARET + traditional ET versus traditional ET only * what are the differences in acceptance and satisfaction of treatment, between ARET + traditional ET and the traditional ET-only group
Trial Details
NCT Number NCT06740487
Lead Sponsor Wayne State University
Collaborators: Ralph H. Johnson VA Medical Center, United States Department of Defense
Conditions
(from sponsor)		 PTSD, Post Traumatic Stress Disorder
Related terms Stress Disorders, Post-Traumatic
Enrollment 40 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov