Virtual reality rehab aims to bring stroke therapy home
NCT ID NCT04620707
First seen Sep 03, 2026 · Last updated Sep 04, 2026 · Updated 1 time
Summary
This trial tests a virtual reality system called RGS that guides stroke survivors through reaching, grasping, and placing virtual objects to aid motor and cognitive recovery. The study enrolls adults who have had a first stroke with mild to moderate arm weakness. Participants use the system in the clinic and then at home for three months, with monitoring via a wearable device. Researchers measure changes in daily functioning and arm movement over a year to see if this approach can extend rehabilitation beyond the clinic.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Rehabilitation Gaming System (RGS), a virtual reality-based training and monitoring device for motor and cognitive rehabilitation
- What this could lead to
- If it works, this could make intensive, personalized rehabilitation available at home for stroke survivors, potentially speeding recovery and improving quality of life.
- What could go wrong
- This is a small early-stage study, and the technology may not prove more effective than standard rehab or may be difficult for some patients to use at home.
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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52 people
The number who actually took part.
- Started
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Nov 2020
- Finished
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Aug 2023
- 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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20 to 85 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: * Patients presenting a first-ever ischemic or intracerebral hemorrhagic stroke. * A CT SCAN and/or MRI had exclude other pathologies. * Lesion localization by clinical symptoms/signs. * Moderate to mild proximal upper limb motor impairment (MRC≥2). * Age 20-85 years old. * Able to sit on a chair or a wheelchair interacting with the RGS during a full session, and be capable and willing to participate in RGS therapy. Exclusion criteria: * Presence of a condition or abnormality that in the opinion of the investigator would compromise the safety of the patient or the quality of the data. * Severe cognitive capabilities that prevent the execution of the experiment (MoCA \< 19). This cut-off score is based on pilot study (Maier, M. et al, 2019). * Arteriovenous malformation or lesions not related with a stroke. * Severe associated impairment such as spasticity, communication disabilities (sensorial, Wernicke aphasia or apraxia), major pain or other neuromuscular impairments or orthopedic devices that would interfere with the correct execution of the experiment (Modified Ashworth Scale \< 3). * Unable to use the RGS independently according to the therapist's observations and lacking support from a caregiver to use the RGS. * Refusal to sign the consent form. * Pre-stroke history of upper limb motor disability.
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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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University Miguel Hernandez - Specs Lab
Elche, Alicante, 03202, Spain
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- 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