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NCT05560113 · ClinicalTrials.gov registry record · NA

Disrupting Fear-based Memory Consolidation

A NA study of Post Traumatic Stress Disorder, sponsored by Emory University.

Recruiting
Registry status
NA
Development phase
66
Enrollment target
2
Study locations

NCT05560113 is a NA study of Post Traumatic Stress Disorder that is actively recruiting participants, run by Emory University. The registered enrollment target is 66 participants, below the 1,116-participant average among 144 other Post Traumatic Stress Disorder trials with a reported enrollment target (94% lower). The trial reports 2 study locations across 1 state.

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The verdict

NCT05560113, a NA study of Post Traumatic Stress Disorder, is actively recruiting participants, sponsored by Emory University.

RECRUITING
Registry status
NA
Development phase
66 participants
Enrollment target
2
Study locations

Study Summary

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.

Interventions

  • OTHER Continuous theta burst stimulation (cTBS)
  • OTHER Sham continuous theta burst stimulation (cTBS)

Study Locations (2)

Georgia

  • Emory Rehabilitation Hospital - Atlanta
  • Emory University Hospital - Atlanta

Trial Details

FieldValue
Enrollment Target 66 participants
Start Date 2022-11-28
Est. Completion 2028-12
Phase NA

Sponsor

Emory University

1,208 total trials

What the Registry Record Tells You About NCT05560113

The ClinicalTrials.gov registry entry for NCT05560113 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 66 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,116-participant average among 144 other Post Traumatic Stress Disorder trials with a reported enrollment target (94% lower). The listed sponsor is Emory University, which has 1,208 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Post Traumatic Stress Disorder appearing as the primary indexed condition, and to 2 interventions - of which Continuous theta burst stimulation (cTBS) is the first listed.

NCT05560113 reports 2 study locations spanning 1 distinct geographic area - top geographies include Georgia.

Frequently Asked Questions

What is clinical trial NCT05560113 about?

NCT05560113 is a clinical study titled "Disrupting Fear-based Memory Consolidation". 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 de...

What is the current status of trial NCT05560113?

This trial is currently recruiting. It is a NA study. The enrollment target is 66 participants. The study started on 2022-11-28. Estimated completion is 2028-12.

What conditions does trial NCT05560113 study?

This clinical trial studies the following conditions: Post Traumatic Stress Disorder.

What interventions are being tested in trial NCT05560113?

The interventions under investigation include: Continuous theta burst stimulation (cTBS) (OTHER), Sham continuous theta burst stimulation (cTBS) (OTHER).

Who is sponsoring clinical trial NCT05560113?

This trial is sponsored by Emory University, which has 1,208 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05560113 being conducted?

This trial has 2 study locations across Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.