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NCT02131129 · ClinicalTrials.gov registry record · NA

rTMS in First Episode Psychosis

A NA study, sponsored by Indiana University.

Completed
Registry status
NA
Development phase
20
Enrollment target

NCT02131129 is a NA study that has completed, run by Indiana University. The registered enrollment target is 20 participants.

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The verdict

NCT02131129, a NA study, has completed, sponsored by Indiana University.

COMPLETED
Registry status
NA
Development phase
20 participants
Enrollment target

Study Summary

This study proposes to examine the application of rTMS for the treatment of cognitive dysfunction in FEP. This is an important population for study because if effective, rTMS may represent a preventative treatment for the development of social and vocational impairment that is associated with cognitive dysfunction in schizophrenia. This study will also seek to refine the understanding of the brain circuitry that mediates the potential pro-cognitive effects of rTMS through the use of functional magnetic resonance imaging (fMRI) at baseline and following the course of rTMS administration.

Interventions

  • DEVICE Sham Comparator
  • DEVICE rTMS

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2014-04-30
Est. Completion 2016-12
Phase NA

Sponsor

Indiana University

890 total trials

What the Registry Record Tells You About NCT02131129

The ClinicalTrials.gov registry entry for NCT02131129 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Indiana University, which has 890 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Sham Comparator is the first listed.

NCT02131129 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02131129 about?

NCT02131129 is a clinical study titled "rTMS in First Episode Psychosis". This study proposes to examine the application of rTMS for the treatment of cognitive dysfunction in FEP. This is an important population for study because if effective, rTMS may represent a preventative treatment for the development of social and vocational impairment that is associated with cognit...

What is the current status of trial NCT02131129?

This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2014-04-30. Estimated completion is 2016-12.

What interventions are being tested in trial NCT02131129?

The interventions under investigation include: Sham Comparator (DEVICE), rTMS (DEVICE).

Who is sponsoring clinical trial NCT02131129?

This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.

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.