Wearable hip robot could bring stroke rehab home
NCT ID NCT07716475
First seen Jul 21, 2026 · Last updated Jul 22, 2026 · Updated 1 time
Summary
This trial tests whether a hip-assisted wearable robot can help stroke survivors improve their walking through at-home training sessions. Eight adults who have had a stroke and walk with a spastic hemiplegic gait will use the robot during four 30-minute sessions over two weeks, guided by a visiting therapist. Researchers will measure usability and walking improvements to see if this approach is practical and effective.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a hip-assisted wearable robot that assists hip movement during walking, used at home with a therapist
- What this could lead to
- If successful, this approach could offer a convenient, home-based rehabilitation option to improve walking after a stroke.
- What could go wrong
- This is a very small, early exploratory trial with only 8 participants, so results may not apply broadly. The device requires a visiting therapist, which may limit practicality.
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 8 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2026
- Expected to finish
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Jul 2027
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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19 to 80 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: 1. Adults aged 19 years or older and under 80 years 2. Persons diagnosed with cerebral infarction or intracerebral hemorrhage confirmed by magnetic resonance imaging or computed tomography 3. Persons for whom at least 1 month has elapsed since the diagnosis of stroke 4. Persons showing a spastic hemiplegic gait pattern due to stroke 5. Patients with a Functional Ambulatory Category score below 4 6. Persons who can sit without assistance at the edge of a bed and can stand for 10 seconds with or without assistance 7. Persons with sufficient cognitive ability to follow simple instructions and understand the content and purpose of the study (Mini-Mental State Examination score \>= 20) Exclusion Criteria: 1. Persons with contraindications to lower-extremity weight bearing, such as severe lower-extremity joint contracture or an untreated fracture 2. Persons for whom wearing the device is difficult due to skin disease or open wounds 3. Persons with a severe difference in the length of the two lower extremities 4. Persons with severe deformity or joint contracture in the lower extremities 5. Persons unable to maintain a sitting posture or a standing posture on their own 6. Persons with severe lower-extremity spasticity (Modified Ashworth Scale (MAS) grade 2 or higher) 7. Persons who cannot cooperate with gait therapy using the robot-assisted orthopedic exercise device due to severe cognitive decline (Mini-Mental State Examination score \< 20), delirium, or severe language function impairment 8. Persons who cannot maintain prolonged standing or walking due to underlying conditions such as orthostatic hypotension or reduced cardiopulmonary function 9. Persons with other concomitant conditions affecting gait, such as peripheral neuropathy or parkinsonism due to alcoholism or severe diabetes 10. Pregnant women or patients with the possibility of pregnancy 11. Persons currently participating in another clinical trial 12. Persons at high risk in the event of a fall or bleeding due to a coagulation disorder or the like 13. Persons with a height less than 140 cm or greater than 190 cm 14. Persons for whom wearing the robot is not possible 15. Persons with clinically significant findings that, in the medical judgment of the principal investigator or a sub-investigator, are considered inappropriate for this study other than the above
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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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Yongin Severance Hospital
RECRUITINGYongin-si, Gyeonggi-do, 16995, South Korea
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Robot could let stroke patients rehab their hands at home without a therapist
- 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