Mind-Controlled hand therapy shows promise for spinal cord injury recovery
NCT ID NCT05637775
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tested whether a brain-computer interface (BCI) training program could improve hand and arm function in people with recent spinal cord injuries. Thirty participants used a system that reads brain signals during hand motor imagery exercises. The goal was to see if this approach could boost brain plasticity and recovery better than standard motor imagery alone.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Brain-computer interface (BCI) training with motor imagery
- What this could lead to
- If successful, this approach could offer a new rehabilitation tool to improve hand and arm function after spinal cord injury.
- What could go wrong
- This is a small, early-stage study (30 participants) with no blinding, so results may not apply widely. The intervention is complex and requires specialized equipment.
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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30 people
The number who actually took part.
- Started
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Nov 2022
- Finished
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Jun 2025
- 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 70 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.
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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: * subacute cervical SCI (30-90 days from event) * classification according to ISNCSCI AIS A-D, lesion level C1-T1 * Upper Extremity Motor Score (UEMS) \< 40 Exclusion Criteria: * other conditions (present or previous) potentially affecting sensorimotor upper limb function * inability to give informed consent and understand the requirements for the training
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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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Neurorehabilitation Units- Fondazione Santa Lucia, IRCCS
Rome, Italy, 00179, Italy
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Breathing brief Low-Oxygen bursts may boost sleep apnea treatment
- Pure oxygen tested as a switch for dormant nerves after spinal cord injury
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