Zapping the brain with precision electricity may supercharge hand rehab after spinal injury
NCT ID NCT05589415
First seen Jul 24, 2026 · Last updated Jul 24, 2026
Summary
This trial tests whether a focused form of brain stimulation called high-definition transcranial direct current stimulation (HD-tDCS) can improve arm and hand function in people with cervical spinal cord injury. Participants receive either HD-tDCS or conventional stimulation during rehabilitation sessions over four weeks. The study measures changes in strength, sensation, and hand dexterity to see if the more targeted electrical field leads to greater recovery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- high-definition transcranial direct current stimulation (HD-tDCS) delivered through a cap with five small electrodes
- What this could lead to
- If it works, this could point toward a more effective way to enhance rehabilitation and improve arm and hand function after spinal cord injury.
- What could go wrong
- This is a small, early-stage trial with only 24 participants, so results may not apply widely. The improvement from stimulation may be modest or absent.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 24 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2020
- Expected to finish
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May 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Provision of signed and dated informed consent form * Stated willingness to comply with all study procedures and availability for the duration of the study * Age between 18 and 75 years * Physician diagnosed cervical incomplete spinal cord injury or lesion (iSCI) * Classified by the American Spinal Cord Association (AIS) impairment scale as AIS C or D * iSCI occurred at least 18 months ago * Level of injury or lesion is between C2 and T1 * Bicep strength must be classified as ≥ 3 muscle grade as defined by the medical research council (MRC) scale * Tricep strength must be at least an MRC grade of 2 and be at least 1 muscle grade lower than bicep * Both the biceps and triceps will be required to elicit an active motor evoked potential \>200 uV with transcranial magnetic stimulation * Must maintain current medication regime * Must present with a weaker side of the body, as indicated by a Upper Extremity Motor Score (UEMS) score difference between the left and right side * UEMS \< 40 (50 max score) Exclusion Criteria: * Pacemaker or other implanted device * Metal in the skull * History of seizures * Pregnancy * First-degree relative with medication-resistant epilepsy * Current participation in upper limb rehabilitation therapies * Current use of illicit drugs, abusing alcohol, or have withdrawn from alcohol in the last 6 months * Other neurological impairment or condition * Pressure ulcers * Significant lower motor neuron loss at C7 as noted by a nerve conduction velocity \<50 m/s * History of traumatic brain injury, as documented by Rancho Scale Impairment of ≤ 5 * History of brain MRI documented focal cerebral cortex infarct (e.g. hydrocephalus) * Contractures at the elbow * Severe spasticity as noted by a Modified Ashworth Scale (MAS) \> 4. * Documented, non-sedated post-traumatic amnesia lasting more than 48 hours * Demonstrated present gains in motor recovery as noted by a \>10% change in triceps strength from pre-test #1 to pre-test #2 * A neuroactive medication that has the potential to lower the seizure threshold
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University of Texas Rio Grande Valley
Harlingen, Texas, 78550, United States
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Other studies related to the condition(s) this trial covers.
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