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NCT03749967 · ClinicalTrials.gov registry record · Phase 1

rTMS for Emotional Difficulties in Verterans

A Phase 1 study, sponsored by VA Office of Research and Development.

Completed
Registry status
Phase 1
Development phase
21
Enrollment target

NCT03749967: Completed Phase 1 study, sponsored by VA Office of Research and Development.

NCT03749967 is a Phase 1 study that has completed, run by VA Office of Research and Development. The registered enrollment target is 21 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03749967, a Phase 1 study, has completed, sponsored by VA Office of Research and Development.

COMPLETED
Registry status
Phase 1
Development phase
21 participants
Enrollment target

Study Summary

Mental illness rarely occurs as a single, easily categorized condition. Instead, multiple disorders often co-occur. This complicates the treatment plan for many Veterans, especially those suffering the most severe dysfunction. This also means that clinical research aimed at one specific disorder may not be optimized to treat the realworld presentation of neuropsychiatric illness. The investigators propose in this study to develop a novel, non-invasive brain stimulation treatment that would promote rehabilitation for Veterans suffering a wide range of emotional difficulties. More specifically, the investigators propose to up-regulate the brain circuitry that supports flexible problem solving and contending with daily demands. Rather than focusing on reducing the symptoms of a specific disorder to reduce the intrusion into daily life, the investigators propose to augment those brain circuits that promote adaptive cognition and thus quality of life.

Interventions

  • DEVICE Repetitive Transcranial Magnetic Stimulation (rTMS)

Trial Details

FieldValue
Enrollment Target 21 participants
Start Date 2019-02-01
Est. Completion 2023-10-28
Phase Phase 1

Sponsor

VA Office of Research and Development

1,668 total trials

What the Registry Record Tells You About NCT03749967

The ClinicalTrials.gov registry entry for NCT03749967 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 21 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is VA Office of Research and Development, which has 1,668 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Repetitive Transcranial Magnetic Stimulation (rTMS) is the first listed.

NCT03749967 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03749967 about?

NCT03749967 is a clinical study titled "rTMS for Emotional Difficulties in Verterans". Mental illness rarely occurs as a single, easily categorized condition. Instead, multiple disorders often co-occur. This complicates the treatment plan for many Veterans, especially those suffering the most severe dysfunction. This also means that clinical research aimed at one specific disorder may...

What is the current status of trial NCT03749967?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 21 participants. The study started on 2019-02-01. Estimated completion is 2023-10-28.

What interventions are being tested in trial NCT03749967?

The interventions under investigation include: Repetitive Transcranial Magnetic Stimulation (rTMS) (DEVICE).

Who is sponsoring clinical trial NCT03749967?

This trial is sponsored by VA Office of Research and Development, which has 1,668 total clinical trials registered on ClinicalTrials.gov.

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, the data changelog, or report a data error.