The goal of this clinical trial is to evaluate whether low-intensity focused ultrasound (LIFU) of the ventral anterior cingulate cortex (vACC) can normalize dysfunctional brain activation patterns and behaviors in frontline healthcare workers with post-traumatic stress disorder. The main questions it aims to answer are: * Does LIFU of the vACC effect activity and connectivity of the vACC and amygdala? * Does LIFU of the vACC reduce post-traumatic stress symptoms? Researchers will compare LIFU to sham modulation to see if LIFU modulates activity of vACC-amygdala circuitry and affects threat sensitivity and emotion regulation. Participants will: * Complete two fMRI sessions (before and after LIFU) * Receive a single session of LIFU or sham modulation of the vACC * Wear a wearable device that tracks sleep and heart rate metrics
The study employs a double-blind, randomized, sham-controlled design to evaluate whether low-intensity focused ultrasound (LIFU) targeting the ventral anterior cingulate cortex (vACC) can normalize fronto-limbic circuitry and reduce post-traumatic stress symptomatology in frontline healthcare workers. Sixty-six frontline healthcare professionals aged 18-65 (PCL-5 ≥ 33 or at least partial PTSD on the MINI) will complete baseline assessments that include structural MRI, resting-state fMRI, and two task-based scans. Concurrently, participants initiate continuous Oura Ring wearable monitoring and daily ecological momentary assessment (EMA) surveys. Subjects will return for active or sham LIFU neuromodulation of the vACC. Before and after LIFU, identical MRI and questionnaire batteries quantify acute neural and behavioral change.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
TRIPLE
Enrollment
66
Low intensity focused ultrasound neuromodulation of the ventral anterior cingulate cortex
Low intensity focused ultrasound with a Sorbothane membrane cover to prevent acoustic energy transmission
Laureate Institute for Brain Research
Tulsa, Oklahoma, United States
RECRUITINGLIFU target engagement
Percent BOLD signal change in vACC and amygdala regions of interest
Time frame: Study day 1 to day 7 (plus or minus 3 days)
Behavioral changes
Change in reaction time (ms) and error rate (percentage of correct answers) on emotional conflict task; difference between optimal and observed flight initiation distance.
Time frame: Day 0 to Day 7 (plus or minus 3 days)
LIFU effects on physiology
Change in heart rate variability (ms), change in resting heart rate (beats per minute), change in %REM sleep (minutes), change in %deep sleep (minutes) as measured by Oura Ring
Time frame: Day 0 to day 14 (plus or minus 6 days)
LIFU effects on PTSD symptoms
Change in PCL-5 score
Time frame: Dy 0 to day 14 (plus or minus 6)
fMRI-heart rate variability correlation
Correlations between vACC/amygdala BOLD signal extracted beta-weights and heart rate variability (ms) as measured by Oura Ring
Time frame: Day 0 to day 14 (plus or minus 6)
fMRI-resting heart rate correlation
Correlations between vACC/amygdala BOLD signal extracted beta-weights and resting heart rate (beats per minute) as measured by Oura ring
Time frame: Day 0 to day 14 (plus or minus 6)
fMRI-REM sleep correlation
Correlations between vACC/amygdala BOLD signal extracted beta-weights and %REM sleep (minutes) as measured by Oura ring
Time frame: Day 0 to day 14 (plus or minus 6)
fMRI-deep sleep correlation
Correlations between vACC/amygdala BOLD signal extracted beta-weights and %deep sleep (minutes) as measured by Oura ring
Time frame: Day 0 to day 14 (plus or minus 6)
fMRI-PTSD Symptom Correlation
Correlations between vACC/amygdala BOLD signal extracted beta-weights and PCL-5 score.
Time frame: Day 0 to day 14 (plus or minus 6)
fMRI-Emotion Regulation Correlation
Correlations between vACC/amygdala BOLD signal extracted beta-weights and Cognitive-Emotion Regulation Questionnaire Score.
Time frame: Day 0 to day 14 (plus or minus 6)
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