PTSD Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who are current or former members of the US Military (Veterans or active Service Members)
- People who have been assessed with PTSD, shown by a score above 33 on a standard PTSD checklist (PCL-5)
- People who have experienced combat trauma or served in a location that qualified for imminent danger pay
- People who are fluent in English
- People who are able to read, understand, and sign a consent form agreeing to the study's requirements
- People who have access to a smartphone or tablet, to use a mobile health app or join a virtual classroom
- People who are willing to complete psychological questionnaires and ongoing assessments throughout the study
- People who are able to complete all assessments independently, are willing to follow all study procedures, and are available for the full duration of the study
Who may not be able to join:
- People who are currently experiencing active thoughts of suicide, as identified by the study investigator at screening or at any point during the study
- People with a significant history of psychotic disorder, bipolar disorder, or a brain/memory-related condition such as dementia, as determined by the study investigator
- People with serious, active substance misuse — including an alcohol use score above 15 on a standard screening tool, or reported use of illicit substances other than cannabis, or cannabis use three or more times per week (confirm with trial site)
- People who are currently receiving another form of treatment more than twice a month, other than general supportive therapy
- People who are currently engaged in specific trauma-focused therapies, including Cognitive Processing Therapy (CPT), Prolonged Exposure (PE), or Eye Movement Desensitization and Reprocessing (EMDR)
- People where the study investigator believes participation could affect the person's safety or the quality of the study results
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Sarah Jackson, PhD, The University of Texas Health Science Center, Houston
Phone: (281) 825-9923
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Reduced symptoms of PTSD as assessed by the Posttraumatic Stress Disorder Checklist for Diagnostic and Statistical Manual of Mental Disorders (DSM-5) (PCL-5); Increasing resilience as assessed by The Connor-Davidson Resilience Scale-10 (CD-RISC-10)4; Satisfaction with care as assessed by the Client Satisfaction Questionnaire-8-item (CSQ-8); Satisfaction with care as assessed by the Client Satisfaction Questionnaire-8 item ( CSQ-8); Satisfaction with care as assessed by the Client Satisfaction Questionnaire (8-item; CSQ-8); Change in average heart rate as assessed by the emWave Inner Balance pe...
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.