Robot suit aims to help stroke and spinal injury patients walk again
NCT ID NCT06805500
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested a new robotic device called REACTION that combines an exoskeleton and a gait trainer to help people with stroke or spinal cord injury improve walking and balance. Seven participants completed two sessions of walking and balance tasks, followed by an interview. The goal was to see if the device is feasible and to measure walking speed and balance.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- REACTION device (combination of exoskeleton and gait trainer)
- What this could lead to
- If successful, this could lead to a new rehabilitation tool that helps improve walking and balance in people with neurological conditions.
- What could go wrong
- This is a very small feasibility study with only 7 participants, so results may not apply to everyone. The device is still in early testing and may not improve walking speed significantly.
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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7 people
The number who actually took part.
- Started
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May 2025
- Finished
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Dec 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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16 years and older
- 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.
In order to be eligible to participate in this study, a participant must meet all of the following criteria: * Age \> 16 years * Able to give informed consent Stroke patients: * first-ever ischemic or haemorrhagic stroke * FAC score between 3 and 4 * (Sub)acute or chronic phase SCI patients: * Neurological injury levels ranging from C5 to T9 * Motor incomplete spinal cord injury (ASIA impairment score of C or D) * Able to walk independently (without physical support) Exclusion Criteria: A potential participant who meets any of the following criteria will be excluded from participation in this study: * Premorbid disability of lower extremity * Progressive neurological diseases like dementia or Parkinson * Skin lesions or severely impaired sensation at the hemiparetic leg * Contraindication for mobilization, like lower limb fracture * Insufficient knowledge of the Dutch language to understand the purpose or meth-ods of the study * Pregnancy
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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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Roessingh Research and Development
Enschede, Netherlands
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Sint Maartenskliniek
Ubbergen, Netherlands
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Other studies related to the condition(s) this trial covers.
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