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Robotic glove and virtual reality team up to rehabilitate Stroke-Affected hands
NCT ID NCT07706621
First seen Jul 16, 2026 · Last updated Jul 17, 2026 · Updated 1 time
Summary
This pilot study tests whether a program called GRIP—which combines a soft robotic glove with a virtual reality system—can help adults recovering from a recent stroke improve hand and arm function. About 20 participants in inpatient rehabilitation will be randomly assigned to receive either the GRIP program or a different therapy, in addition to their usual care. The study measures motor improvement, safety, and how well patients accept the therapy over about six weeks.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a soft robotic glove with virtual-reality training (GRIP program)
- What this could lead to
- If successful, this approach could offer a new, engaging way to improve hand and arm function during stroke rehabilitation.
- What could go wrong
- This is a small pilot study with only 20 participants, so results may not apply to everyone. The therapy may not lead to significant improvements over standard care.
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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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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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: * First unilateral stroke (\<6-month post-stroke at enrollment) * ≥18 years old * Hand sensorimotor impairments * Able to understand and follow a two-step instruction * Admitted to the rehabilitation center and participating in the stroke program Exclusion Criteria: * Severe spasticity (score ≥3 on the Modified Ashworth Scale) * Unilateral spatial neglect * Moderate to severe hand pain * Significant motor impairment of the fingers (active finger flexion/extension less than 10°) * Any medical condition that may interfere with participation
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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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Institut de réadaptation Gingras-Lindsay-de-Montréal
Montreal, Quebec, H3S 2J4, Canada
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
- Can a PET tracer reveal hidden brain inflammation?