← Eichor
Study identifier: NCT06214208 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Influence of Spinal Stimulation Frequency on Spasticity, Motor Control, and Pain After Spinal Cord Injury

Condition: Spinal Cord Injuries  ·  Sponsor: Shepherd Center, Atlanta GA

PhaseNA
Planned participants36
Who can joinAll sexes, 16 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this study is to identify the effect of different types of noninvasive spinal stimulation on spasticity (involuntary muscle activity), muscle strength, and pain in people with spinal cord injury. The spinal stimulation consists of electrical stimulation applied through one electrode over the skin of the lower back and two electrodes over the stomach. Testing will include participating in measurements before the intervention, during intervention, and immediately after the intervention. This study requires participants to come into Shepherd Center 4 consecutive days a week for 2-3 hours per day across 2-3 weeks.

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

Talk to the study team

Jaclyn Miller, PT, DPT  ·  404-350-7638  ·  jaclyn.miller@shepherd.org

Evan Sandler, PT, DPT  ·  404-603-4175  ·  evan.sandler@shepherd.org

Always discuss trial participation with your own doctor first.

Locations (1)

Shepherd Center, Inc.Atlanta, Georgia, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06214208