Robotic glove may help stroke survivors regain hand control
NCT ID NCT07701577
First seen Jul 14, 2026 · Last updated Jul 15, 2026 · Updated 1 time
Summary
This study tests whether a robotic hand device can improve grip strength and fine motor skills in people who had a stroke at least six months ago. Participants use the HWARD exoskeleton, which assists hand opening and closing, during 45-minute sessions three times a week for 12 weeks. The goal is to see if robot-assisted training helps restore hand function better than standard therapy alone.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- robot-assisted training using the In motion robotic gym system (HWARD device)
- What this could lead to
- If effective, this robotic training could become a standard therapy to help stroke survivors regain hand function and independence.
- What could go wrong
- This is a small, early-stage study with 34 participants, so results may not apply to all stroke patients. The device may not outperform conventional therapy.
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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34 people
The number who actually took part.
- Started
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May 2025
- Finished
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May 2026
- 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 60 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 ranged from 40 to 60 years old. * Clinical diagnosis of ischemic stroke and diagnosis confirmed by CT or MRI with hand impairments. * Stroke started since six months (at chronic stage) * Mild to moderate upper limb functional limitation according to (Fugl-Meyer score: 85-99). * Ability to understand and follow instructions and to provide informed consent. Exclusion Criteria: * More than one stroke. * Other current significant impairment of the upper limb affected by stroke, e.g. fixed contracture, frozen shoulder, severe arthritis, recent fracture. * Diagnosis likely to interfere with rehabilitation or outcome assessments, e.g. registered blind. * Previous use of the InMotion robotic gym system or other arm rehabilitation robot. * Current participation in a rehabilitation trial evaluating upper limb rehabilitation after stroke
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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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Cairo University
Cairo, Cairo Governorate, 11432, Egypt
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Effects of transcranial direct current stimulation and pelvic proprioceptive neuromuscular facilitation on trunk control, balance and functional mobility in stroke patients
- Correlation of visual and motor deficits in stroke patients
- Pilot study on the effects induced by an electromyographic-controlled functional electrical stimulator (FitFES) for upper limb rehabilitation in post-stroke patients
- Brazilian version of a behavior change intervention to support healthy lifestyle adoption after stroke - iVIDAVC: protocol for a pilot randomized study
- Determination of efficacy of sustained motor contraction generated using StimWave peripheral nerve stimulator
- Safety and preliminary efficacy of NXL-001 in patients with ischemic stroke