Home robot aims to get stroke patients back on their feet
NCT ID NCT07250425
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests a new robotic walking trainer called Rise&Walk InHome that stroke survivors can use at home. Twenty adults who had a stroke 3 months to 5 years ago will either use the device for 30 minutes, 4 times a week plus usual care, or just usual care. The goal is to see if the device is safe, easy to use, and helps improve walking distance and speed.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Rise&Walk InHome robotic gait training device
- What this could lead to
- If successful, this could provide an affordable, home-based option to help stroke survivors improve walking ability and reduce fall risk.
- What could go wrong
- This is a small, early feasibility study with only 20 participants. The device may not be effective for everyone, and home use could pose safety or adherence challenges.
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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About 20 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2026
An estimate. End dates often move.
- 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 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age ≥ 18 years. * First-ever ischemic or hemorrhagic stroke confirmed by medical record. * 3 months to 5 years post-stroke at time of enrollment. * Presence of lower-extremity motor impairment limiting walking function. * Able to stand for at least 30 minutes with no more than minimal assistance (with or without a device). * Medically stable and cleared by a physician to participate in moderate-intensity ambulation exercise. * Living in a home environment that can safely accommodate device installation (e.g., adequate space, appropriate flooring, and power access) as determined by the study team. * Able to understand study procedures and provide informed consent (or have a legally authorized representative), with sufficient cognitive and communication skills to follow simple instructions. * If assistance is required for transfers or device set-up, availability of a caregiver or assistant willing to participate in training and device use. Exclusion Criteria: * Unstable cardiovascular, respiratory, or other medical conditions that contraindicate moderate- to high-intensity walking exercise (e.g., unstable angina, decompensated heart failure, uncontrolled arrhythmias). * Severe musculoskeletal or orthopedic conditions limiting safe participation in supported stepping (e.g., unstable fractures, severe contractures preventing positioning in the device). * Severe spasticity or movement disorders that would preclude safe use of the device, based on investigator judgment. * Severe cognitive impairment, aphasia, or behavioral disturbance that would prevent informed consent or safe participation. * Progressive neurological conditions (e.g., progressive neurodegenerative disease) expected to significantly worsen over the 12-week study period. * Current participation in another interventional trial targeting gait or lower-extremity function. * Any other condition that, in the opinion of the investigators, would make participation unsafe or interfere with study adherence or outcome interpretation.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Kessler Foundation
West Orange, New Jersey, 07052, United States
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Other studies related to the condition(s) this trial covers.
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