RecruitingNot ApplicableNCT05553353

Dosing rTMS for Depression Post-SCI

Evaluating a Novel Method to Determine the rTMS Dose Needed for Treating Depression After Spinal Cord Injury


Sponsor

VA Office of Research and Development

Enrollment

24 participants

Start Date

Mar 31, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Depression is a leading cause of disability worldwide and is more commonly seen in individual's post-spinal cord injury (SCI) than in the general population. Depression post-SCI impacts an individuals' quality of life and recovery. It has been reported that among Veterans with an SCI, those without depression live longer than those with depression. Thus, depression must be treated appropriately. Repetitive transcranial magnetic stimulation (rTMS) is an FDA-approved treatment for depression, but dosing is based on a motor response or movement in the thumb. Over half of individuals with SCI have some degree of arm or hand impairment, so these individuals might not be eligible for rTMS, or they may receive the wrong dose. This study proposes clinical trial in individuals with depression post-SCI to assess the anti-depressant effect of a novel technique to dose rTMS that does not require a motor response in the thumb. By gaining a better understanding of the application of rTMS for depression post-SCI, the investigators aim to advance the rehabilitative care of Veterans.


Eligibility

Min Age: 18 YearsMax Age: 60 Years

Plain Language Summary

Simplified for easier understanding

This study is testing the best dosing of repetitive transcranial magnetic stimulation (rTMS) — a non-invasive brain stimulation technique — for treating depression in people who have had a spinal cord injury. **You may be eligible if:** - You had a cervical or thoracic spinal cord injury at least 6 months ago - You are between 18 and 60 years old - You have been diagnosed with major depression - Your depression score (Hamilton scale) is above 18 - You are not currently on antidepressants, or your medication dose has been stable for at least 4 weeks **You may NOT be eligible if:** - You have dementia or other neurological conditions - You have significant cognitive impairment - You have a history of psychosis or bipolar disorder - You have claustrophobia - You have metal implants in your head, a cochlear implant, or a pacemaker - You have a history of seizures or take anti-seizure medications - You are pregnant - You have had a suicide attempt in the last two years or have active suicidal thoughts Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICErepetitive transcranial magnetic stimulation--Active

Repetitive transcranial magnetic stimulation (rTMS) is a type of non-invasive brain stimulation. An active coil will be used to administer the active rTMS.

DEVICErepetitive transcranial magnetic stimulation--Sham

Repetitive transcranial magnetic stimulation (rTMS) is a type of non-invasive brain stimulation. A sham coil will be used to administer the sham rTMS.


Locations(1)

Ralph H. Johnson VA Medical Center, Charleston, SC

Charleston, South Carolina, United States

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NCT05553353


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