← Eichor
Study identifier: NCT05560113 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Disrupting Fear-based Memory Consolidation

Condition: Post-Traumatic Stress Disorder  ·  Sponsor: Emory University

PhaseNA
Planned participants66
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

This project represents a unique collaborative opportunity to pursue the essential proof-of-principle demonstration that non-invasive interference of sensory cortical memory consolidation shortly after an emotional experience can attenuate the cued fear response and potentially reduce the risk of developing post-traumatic stress disorder (PTSD). If successful, the study results would anchor a potential advance in the treatment of patients after a traumatic event and seed future animal and clinical studies of emotional sensory cortical memory consolidation to reduce the prevalence and negative sequelae of PTSD.

This description comes directly from the study's public registry record.

Talk to the study team

Michael Borich, PhD  ·  404-712-5512  ·  michael.borich@emory.edu

Jennifer Stevens, PhD  ·  404-778-1698  ·  jswils4@emory.edu

Always discuss trial participation with your own doctor first.

Locations (2)

Emory Rehabilitation HospitalAtlanta, Georgia, United StatesRecruiting
Emory University HospitalAtlanta, Georgia, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT05560113