Viewing Study NCT02367521



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Last Modification Date: 2024-10-26 @ 11:38 AM
Study NCT ID: NCT02367521
Status: COMPLETED
Last Update Posted: 2018-08-31
First Post: 2015-02-09

Brief Title: Repetitive Transcranial Magnetic Stimulation rTMS for the Treatment of Depression Other Neuropsychiatric Symptoms After Traumatic Brain Injury TBI
Sponsor: Johns Hopkins University
Organization: Johns Hopkins University

Study Overview

Official Title: Repetitive Transcranial Magnetic Stimulation rTMS for the Treatment of Depression Other Neuropsychiatric Symptoms After Traumatic Brain Injury TBI
Status: COMPLETED
Status Verified Date: 2018-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: rTMS TBI
Brief Summary: Traumatic brain injury TBI is frequently complicated by depression and other problems such as post traumatic stress disorder PTSD sleep disturbance cognitive deficits and behavioral problems Untreated depression can lead to reduced productivity and poor global outcome There is no Food and Drug Administration FDA approved drug for the treatment of TBI-related depression The overarching goal of this small study is to determine the effectiveness of low frequency right LFR rTMS for the treatment of post-TBI depression and co-occurring psychiatric symptoms Repetitive transcranial magnetic stimulation rTMS is a brain stimulation technique It involves generating a brief magnetic field in a coil that is placed on the scalp The magnetic field passes through the skull and induces a weak electrical current in the brain that briefly activates neural circuits at the stimulation site Adults aged 18 and older with a history of head injury of mild or moderate severity who are currently experiencing symptoms of clinical depression may join the study
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: True
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None