New wearable device aims to improve walking after stroke
NCT ID NCT06269367
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested a low-cost wearable device called NewGait to see if it can help stroke survivors walk better. Twenty chronic stroke survivors tried the device and a similar one, while researchers measured their walking speed and muscle activity. The goal is to create an affordable, easy-to-use tool for home rehabilitation.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- NewGait wearable limb orthotic device
- What this could lead to
- If it works, this could provide an affordable, easy-to-use device for stroke survivors to improve walking at home.
- What could go wrong
- This is a very small, early study (20 people) testing short-term effects only. It may not lead to lasting improvements or work for all stroke survivors.
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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20 people
The number who actually took part.
- Started
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Apr 2024
- Finished
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Dec 2024
- 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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40 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.
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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: * Unilateral cortical or subcortical stroke * Chronic stroke (≥ 6 months) At least 6 months following their first unilateral stroke * Able to walk independently with/without assistive devices for 5-10 mins (\~150m) * No significant cognitive deficits as determined by the Mini Mental State Examination (MMSE) score (score≥ 22) Exclusion Criteria: * Cerebellar stroke * Traumatic or vascular brain injury * History of unstable heart condition, uncontrolled diabetes/hypertension * History of a recent lower-extremity trauma or fracture * History of a recent significant orthopedic or neurological conditions that could limit walking ability (e.g., multiple sclerosis, total knee replacement) * Documented history of significant spatial neglect * ankle joint contractures or significant spasticity in the lower limbs * History of a recent Botulinum Toxin (Botox) injection to the lower-extremity muscles (≤ 3 months) * Pregnant or actively planning to become pregnant (self-reported)- Inability to communicate or unable to consent
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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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Physical Medicine & Rehabilitation 325 E Eisenhower Pkwy Suite 3011
Ann Arbor, Michigan, 48108, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- 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