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Robot therapy helps stroke patients regain arm movement
NCT ID NCT06870682
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This pilot study tested a new robot-based therapy program to improve arm function in 10 people who had a stroke at least 6 months ago. The program combined robot-assisted training, practice with daily activities, and home exercises over 4 weeks. The goal was to see if the approach is feasible and potentially helpful for improving movement and sensation in the affected arm.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- robot-based upper limb rehabilitation program
- What this could lead to
- If this approach works, it could point toward a new therapy to improve arm and hand function in people who have had a stroke.
- What could go wrong
- This is a very small pilot study with only 10 participants, so results may not apply to everyone. The therapy is intensive and requires frequent visits, which may not be feasible 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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10 people
The number who actually took part.
- Started
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Feb 2025
- Finished
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Oct 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.
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. Written informed consent must be obtained prior to any screening procedures 2. A first-ever unilateral, supra-tentorial stroke, as defined by WHO (rapidly developing clinical signs of focal (or global) disturbance of cerebral function, with symptoms lasting 24 hours or longer or leading to death, with no apparent cause other than vascular origin) 3. ≥18 years old 4. Being in the chronic phase after stroke, i.e. \> 6 months post stroke 5. Motor impairment in the upper limb, defined as Fugl-Meyer score \>22 out of 66 to demonstrate moderate to full upper limb motor function (patients scoring \<23 out of 66 will not be able to comply with the KINARM protocol) 6. Residual sensory upper limb impairment, defined as Tactile Discrimination Test score \<24 out of 25 7. Impaired functionality, defined as Action Research Arm Test score \<52 out of 57 8. Manageable spasticity for KINARM tasks Exclusion Criteria: 1. Having musculoskeletal and/or other neurological disorders impacting care or prognosis 2. Having severe communication or cognitive deficits that interfere with the protocol 3. Any disorder, which in the investigator's opinion might jeopardise participant's safety or compliance with the CIP 4. Contraindications for robot-based therapy (e.g., uncontrolled epilepsy) 5. Participation in another clinical investigation 6. Having uncontrolled head movements (e.g. tremor), only relevant if participant is willing to receive the additional fNIRS assessments 7. Having any contra-indications for MRI, only relevant if participant is willing to receive the additional MRI assessments: * Pacemaker * Implantable Cardioverter Defibrillator (ICD) * Cochlear implant * Internal Insulin-pump * Deep brain stimulation * Any other metal device in body * Claustrophobia * Having a history of a neuropsychiatric or neurologic disorder before the diagnosis of stroke (e.g., depression, traumatic brain injury) * Use of psychoactive medication before the diagnosis of stroke (e.g., anti-depressive medication) * Use (or history of use) of drugs/alcohol * Being pregnant
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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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KU Leuven
Leuven, 3001, Belgium
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
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- Heart hole or stroke trigger? global registry tracks who gets closure and what happens next