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RECRUITING NA

A Study of a Novel EEG Neurofeedback System for PTSD Treatment

NCT06770998 · View on ClinicalTrials.gov ↗

Study Summary

The goal of this clinical trial is to learn if training with the Prism system can reduce PTSD symptoms in US military Veterans and civilians with PTSD. Prism is a form of neurofeedback training that uses EEG signals to promote self-regulation of brain function. The main question this study aims to answer is: Does Prism training lead to decreased PTSD symptoms in US Veterans and civilians when used in addition to usual PTSD treatment? Researchers will compare Prism training to a sham training (a look-alike training that does not provide real feedback on brain activity) to see if Prism training decreases PTSD symptoms. Participants will: * Complete two one-hour in-person training sessions a week for about 8 weeks (15 sessions) * Complete two booster training sessions one month and two months after finishing the main training course * Participate in three detailed interviews: one before training, a second after nine weeks of training, and a third one month after the last booster training session (about 20 weeks after the initial visit)

Interventions

  • DEVICE EEG-neurofeedback training
  • DEVICE Sham training

Study Locations (6)

New York

  • New York University Grossman School of Medicine — New York
  • University of Rochester Medical Center (URMC) — Rochester

Alabama

  • Birmingham VA Medical Center — Birmingham

Georgia

  • Atlanta VA Medical Center — Decatur

Massachusetts

  • Boston VA Healthcare System — Boston

South Carolina

  • Charleston VA Medical Center — Charleston

Trial Details

FieldValue
Enrollment Target 250 participants
Start Date 2025-05-14
Est. Completion 2027-08
Phase NA

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06770998

The ClinicalTrials.gov registry entry for NCT06770998 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 250 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Foundation for Atlanta Veterans Education and Research, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Stress Disorders, Post-Traumatic appearing as the primary indexed condition, and to 2 interventions — of which EEG-neurofeedback training is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06770998 reports 6 study locations spanning 5 distinct geographic areas — top geographies include New York, Alabama, Georgia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06770998 about?

NCT06770998 is a clinical study titled "A Study of a Novel EEG Neurofeedback System for PTSD Treatment". The goal of this clinical trial is to learn if training with the Prism system can reduce PTSD symptoms in US military Veterans and civilians with PTSD. Prism is a form of neurofeedback training that uses EEG signals to promote self-regulation of brain function. The main question this study aims to a...

What is the current status of trial NCT06770998?

This trial is currently recruiting. It is a NA study. The enrollment target is 250 participants. The study started on 2025-05-14. Estimated completion is 2027-08.

What conditions does trial NCT06770998 study?

This clinical trial studies the following conditions: Stress Disorders, Post-Traumatic. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06770998?

The interventions under investigation include: EEG-neurofeedback training (DEVICE), Sham training (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06770998?

This trial is sponsored by Foundation for Atlanta Veterans Education and Research, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06770998 being conducted?

This trial has 6 study locations across Alabama, Georgia, Massachusetts, New York, South Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial