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Study identifier: NCT05553353 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Dosing rTMS for Depression Post-SCI

Condition: Spinal Cord Injuries · Depression · Depressive Disorder, Major  ·  Sponsor: VA Office of Research and Development

PhaseNA
Planned participants24
Who can joinAll sexes, 18 Years to 60 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Catherine J VanDerwerker, PhD DPT PT  ·  (843) 792-5047  ·  catherine.vanderwerker@va.gov

Sarah A Jackson, BA MA  ·  (843) 789-6700  ·  sarah.jackson@va.gov

Always discuss trial participation with your own doctor first.

Locations (1)

Ralph H. Johnson VA Medical Center, Charleston, SCCharleston, South Carolina, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05553353