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NCT03819608 · ClinicalTrials.gov registry record · NA

Neuromodulation and Neurorehabilitation for mTBI

A NA study of Post Traumatic Stress Disorder and Mild Traumatic Brain Injury, sponsored by Northwestern University.

Recruiting
Registry status
NA
Development phase
200
Enrollment target
2
Study locations

NCT03819608 is a NA study of Post Traumatic Stress Disorder and Mild Traumatic Brain Injury that is actively recruiting participants, run by Northwestern University. The registered enrollment target is 200 participants, below the 1,115-participant average among 144 other Post Traumatic Stress Disorder trials with a reported enrollment target (82% lower). The trial reports 2 study locations across 2 states.

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The verdict

NCT03819608, a NA study of Post Traumatic Stress Disorder and Mild Traumatic Brain Injury, is actively recruiting participants, sponsored by Northwestern University.

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

Study Summary

This study will determine (i) the magnitude of immediate and sustained effects of a current clinical standard interactive computer attention processing training (APT) when combined with intermittent theta burst stimulation (iTBS), a type of repetitive transcranial magnetic stimulation and (ii) determine how APT + iTBS changes the neurocognitive system of attention in individuals with persistent attention deficits related to mTBI +/- PTSD.

Conditions Studied

Post Traumatic Stress Disorder Mild Traumatic Brain Injury

Interventions

  • DEVICE real iTBS
  • BEHAVIORAL real APT
  • BEHAVIORAL placebo APT
  • DEVICE placebo iTBS

Study Locations (2)

Illinois

  • Northwestern University - Chicago

Texas

  • Moody Neurorehabilitation Institute - Houston

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2021-04-01
Est. Completion 2025-12
Phase NA

Sponsor

Northwestern University

1,209 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03819608

The ClinicalTrials.gov registry entry for NCT03819608 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 200 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 (82% lower). The listed sponsor is Northwestern University, which has 1,209 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Post Traumatic Stress Disorder appearing as the primary indexed condition, and to 4 interventions - of which real iTBS is the first listed.

NCT03819608 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Illinois, Texas.

Frequently Asked Questions

What is clinical trial NCT03819608 about?

NCT03819608 is a clinical study titled "Neuromodulation and Neurorehabilitation for mTBI". This study will determine (i) the magnitude of immediate and sustained effects of a current clinical standard interactive computer attention processing training (APT) when combined with intermittent theta burst stimulation (iTBS), a type of repetitive transcranial magnetic stimulation and (ii) deter...

What is the current status of trial NCT03819608?

This trial is currently recruiting. It is a NA study. The enrollment target is 200 participants. The study started on 2021-04-01. Estimated completion is 2025-12.

What conditions does trial NCT03819608 study?

This clinical trial studies the following conditions: Post Traumatic Stress Disorder, Mild Traumatic Brain Injury.

What interventions are being tested in trial NCT03819608?

The interventions under investigation include: real iTBS (DEVICE), real APT (BEHAVIORAL), placebo APT (BEHAVIORAL), placebo iTBS (DEVICE).

Who is sponsoring clinical trial NCT03819608?

This trial is sponsored by Northwestern University, which has 1,209 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03819608 being conducted?

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

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