Shock to the system: brain stimulation may boost stroke rehab
NCT ID NCT03666533
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tested whether adding a mild electrical brain stimulation called tDCS to physical therapy could improve walking in people who had a stroke. 44 participants who were at least 6 months post-stroke received either real or fake tDCS while doing gait exercises in a virtual reality setting. The goal was to see if the brain boost could lead to faster, safer walking.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- transcranial Direct Current Stimulation (tDCS)
- What this could lead to
- If it works, this could offer a simple, low-cost way to boost walking recovery after stroke when added to standard physical therapy.
- What could go wrong
- This was a small, early-stage study (44 people) with no phase designation, so results may not apply widely. tDCS effects can be subtle and inconsistent.
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
-
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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44 people
The number who actually took part.
- Started
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Sep 2018
- Finished
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Mar 2024
- Lead sponsor
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A government agency
The lead sponsor is a US federal agency other than the NIH.
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 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Medically and psychologically stable and at least 6 months after first ever unilateral stroke * Cognition sufficiently intact to give valid informed consent to participate * FMLE score \>15; and ability to actively dorsiflex the paretic ankle in synergy (FMLE item II Flexor synergy-ankle dorsiflexion score 1). * Sufficient endurance to participate in the study Exclusion Criteria: * Activity tolerance is insufficient to complete treadmill training * Inability to produce a trace contraction of ankle dorsiflexors in synergy * Normal ankle dorsiflexion/knee flexion on FMLE standing items (FMLE item IV score=4) * Stroke affecting both sides * Contraindications for rTMS according to the most recent TMS-use guidelines * Contraindications for MRI * Inability to understand English
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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
-
Louis Stokes VA Medical Center, Cleveland, OH
Cleveland, Ohio, 44106-1702, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Robot could let stroke patients rehab their hands at home without a therapist
- Moving patterns may help stroke survivors read faster
- Vibrating wearables put stroke walking to the test
- Robot plus electrical stimulation aims to rebuild arm movement after stroke
- Can a checklist and heart monitor stop repeat strokes?
- Heart hole or stroke trigger? global registry tracks who gets closure and what happens next