Enhancing Cognitive Processing Therapy for Posttraumatic Stress Disorder Via Stellate Ganglion Block Treatment: A Pilot Trial

Who can take part

• Are 18 years or older
• Are fluent in English
• Reside in Illinois
• Have safe transportation means other than driving themselves to Rush University Medical Center for two separate procedures (e.g., Uber, family or friend to drive them to study visits, etc.)
• Have experienced a Criterion A traumatic event during their lifetime
• Have a PTSD diagnosis verified via the Clinician Administered PTSD Scale for DSM-5
• Have not previously received stellate ganglion blocks
• Are willing and able to participate in daily Cognitive Processing Therapy over the course of one week
• Are willing and able to complete self-report measures and clinician-rated assessments at multiple time points over the course of the study

Who cannot take part

• They have not been on a stable dose of psychotropic medication for at least one month by the time of the baseline assessment or are planning to change their medications within 3 months of starting their participation in the study
• They have completed an evidence-based cognitive behavioral PTSD treatment (e.g., Cognitive Processing Therapy or Prolonged Exposure) in the past 12 months or are currently receiving an evidence-based PTSD treatment
• They are currently on any blood-thinning medications or have a coagulopathy
• They have an intellectual disability or significant cognitive impairment that would prevent them from engaging in CPT, as assessed via the Mini-Mental State Exam-Second Edition (MMSE-2)
• They have any of the following conditions: a recent myocardial infarction, glaucoma, a pre-existing contralateral nerve palsy, severe emphysema or a cardiac conduction blockade
• They are allergic to any of the medications injected (i.e., ropivacaine, lidocaine, propofol, medications)
• They have an active infection
• They have a serious or unstable medical illness or instability for which hospitalization may be likely within the next year
• They have a visual or auditory impairment that would prevent them from fully participating in study activities
• The traumatic event occurred in the past month
• They are currently suicidal or homicidal (i.e., plan and intent)
• They have unmanaged psychosis or mania
• They are involved with current legal actions related to the traumatic event that is anticipated to be targeted during treatment
• Subjects who, at the time of consent, appear to have extenuating life circumstances (e.g., unstable housing, no internet access, etc.) which, in the judgement of the Principal Investigator, could affect the ability to deliver the intervention with fidelity