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 able to give informed consent and follow the instructions required by the study
- People who have been randomised into a specific related clinical trial titled "Combining Stellate Ganglion Block with Prolonged Exposure for PTSD: A Randomized Clinical Trial" (NCT05889741)
- People who are willing to wear a sleep monitoring device called the Sleep Profiler and complete self-report questionnaires
Who may not be able to join:
- People who have a pre-existing skin or soft tissue condition on their head that would prevent them from wearing the Sleep Profiler headband comfortably or safely
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: Kristi E Pruiksma, PhD, DBSM, The University of Texas Health Science Center at San Antonio
Phone: (210) 562-6700
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
Total Sleep Time; Wake time after sleep onset; Rapid Eye Movement (REM) sleep state
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.