Robot-Assisted walking program shows promise for brain injury recovery
NCT ID NCT05934773
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a personalized walking and balance training program using a KineAssist robotic treadmill for people recovering from traumatic brain injury, stroke, or other acquired brain injuries. The goal was to safely challenge and improve walking speed, balance, strength, and endurance. Only 5 participants were enrolled before the study was terminated, so the results are not conclusive.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- KineAssist robotic treadmill
- What this could lead to
- If successful, this program could offer a new way to help people with brain injuries improve their walking and balance during rehab.
- What could go wrong
- The trial was terminated early with only 5 participants, so results are very limited. It is unclear if the program works better than standard care.
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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5 people
The number who actually took part.
- Started
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Aug 2022
- Finished
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Apr 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 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.
Inclusion Criteria: * Adults ages 18 years and older * All demographic groups will be invited to participate and would have equal access * Post-TBI individuals currently enrolled at the Moody Neurorehabilitation Institute * Ambulatory with or without assistive devices * Subjects with expressive aphasia in the case of a caregiver able to provide assistance when needed * English-speaking or have a certified interpreter that is English-speaking who will be present for interpretation during the study * Medically stable (controlled hypertension, no arrhythmia, stable cardiovascular status) * Able to provide written informed consent Exclusion Criteria: * Subjects with loss of lower limb * History of serious cardiac disease (e.g., myocardial infarction) * Uncontrolled blood pressure (systolic pressure \>140 mmHg, diastolic blood pressure \>90 mmHg) * Subjects with receptive aphasia * Presence of cerebellar and brainstem deficits * Severe cognitive disorder * Uncontrolled respiratory or metabolic disorders * Major or acute musculoskeletal problems * Spasticity management that included phenol block injections within 12 months or botulinum toxin injections within 4 months of the study * Body weight greater than 250 pounds (due to robotic device weight restrictions)
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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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Moody Neurorehabilitation Institute
Galveston, Texas, 77550, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a checklist and heart monitor stop repeat strokes?