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NCT03932773 · ClinicalTrials.gov registry record · NA

Multi-site Confirmatory Efficacy Treatment Trial of Combat-related PTSD

A NA study of Post Traumatic Stress Disorder, sponsored by The University of Texas at Dallas.

Recruiting
Registry status
NA
Development phase
330
Enrollment target
3
Study locations

NCT03932773 is a NA study of Post Traumatic Stress Disorder that is actively recruiting participants, run by The University of Texas at Dallas. The registered enrollment target is 330 participants, below the 1,115-participant average among 144 other Post Traumatic Stress Disorder trials with a reported enrollment target (70% lower). The trial reports 3 study locations across 2 states.

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The verdict

NCT03932773, a NA study of Post Traumatic Stress Disorder, is actively recruiting participants, sponsored by The University of Texas at Dallas.

RECRUITING
Registry status
NA
Development phase
330 participants
Enrollment target
3
Study locations

Study Summary

The purpose of this study is to examine the benefits of combining repetitive Transcranial Magnetic Stimulation (rTMS) coupled with Cognitive Processing Therapy (CPT) in treating combat-related Posttraumatic Stress Disorder (PTSD) symptoms. The study will also examine change in depression, psychosocial functioning, and neurophysiological (i.e., electroencephalography and magnetic resonance images) measures.

Interventions

  • BEHAVIORAL Cognitive Processing Therapy
  • DEVICE Active rTMS
  • DEVICE Sham rTMS

Study Locations (3)

Texas

  • Metrocare Services of Dallas - Addison
  • The University of Texas at Dallas - Dallas

Florida

  • Florida State University College of Medicine - Tallahassee

Trial Details

FieldValue
Enrollment Target 330 participants
Start Date 2019-05-01
Est. Completion 2026-07-31
Phase NA

Sponsor

The University of Texas at Dallas

50 total trials

What the Registry Record Tells You About NCT03932773

The ClinicalTrials.gov registry entry for NCT03932773 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 330 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,115-participant average among 144 other Post Traumatic Stress Disorder trials with a reported enrollment target (70% lower). The listed sponsor is The University of Texas at Dallas, which has 50 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 3 interventions - of which Cognitive Processing Therapy is the first listed.

NCT03932773 reports 3 study locations spanning 2 distinct geographic areas - top geographies include Texas, Florida.

Frequently Asked Questions

What is clinical trial NCT03932773 about?

NCT03932773 is a clinical study titled "Multi-site Confirmatory Efficacy Treatment Trial of Combat-related PTSD". The purpose of this study is to examine the benefits of combining repetitive Transcranial Magnetic Stimulation (rTMS) coupled with Cognitive Processing Therapy (CPT) in treating combat-related Posttraumatic Stress Disorder (PTSD) symptoms. The study will also examine change in depression, psychosoci...

What is the current status of trial NCT03932773?

This trial is currently recruiting. It is a NA study. The enrollment target is 330 participants. The study started on 2019-05-01. Estimated completion is 2026-07-31.

What conditions does trial NCT03932773 study?

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

What interventions are being tested in trial NCT03932773?

The interventions under investigation include: Cognitive Processing Therapy (BEHAVIORAL), Active rTMS (DEVICE), Sham rTMS (DEVICE).

Who is sponsoring clinical trial NCT03932773?

This trial is sponsored by The University of Texas at Dallas, which has 50 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03932773 being conducted?

This trial has 3 study locations across Florida, Texas. 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 Editorial

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.