Stroke survivors try VR games at home to regain arm control and balance
NCT ID NCT06409598
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether stroke survivors could use non-immersive virtual reality exercises at home to improve arm function and balance. Twenty-seven people with chronic stroke (more than 6 months since their stroke) participated in an 8-week program. The exercises were designed as games to make rehabilitation more engaging. The study focused on whether the program was feasible and acceptable, and also measured changes in arm movement and balance.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Non-immersive virtual reality home-based exercise program
- What this could lead to
- If successful, this could offer a convenient, engaging way for stroke survivors to continue rehabilitation at home, potentially improving arm movement and balance.
- What could go wrong
- This is a small pilot study with only 27 participants, so results may not apply to everyone. The exercises are designed for symptom ease, not a cure, and benefits may be modest.
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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27 people
The number who actually took part.
- Started
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Jul 2024
- Finished
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Apr 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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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: * Age \> 18 years old. * Having stroke for more than 6 months (early or late chronic stage). * Not participating in any other rehabilitation study. * Able to read in English. * Has good internet connection at home, or can the investigator give them a sim card. * Score ≤2 on the Modified Ashworth Scale. * Any degree of upper limb impairment due to stroke (Fugl-Meyer Assessment (FMA)-UE score \<57). * Having sufficient space at home. * The participant should have a laptop, computer at their home, if they don't have any of that, the investigator can loan them a laptop. Exclusion Criteria: * Having severe arm, leg, or spine contractures, or deformities (MAS 3 or 4). * Having any medical contraindications (seizure disorders, symptomatic shoulder subluxation, artificial cardiac pacemaker device, persistent shoulder pain (\> 5 on VAS scale as an average). * To ensure patients had sufficient cognitive abilities to participate in training and evaluation and to provide informed consent, the investigators will exclude patients diagnosed with - serious aphasia (cannot read the instructions) or cognitive dysfunction (inability to understand and follow two-stage instructions given by the investigators. * To avoid potential confounding effects associated with other treatments, patients with any history of virtual reality upper-limb training or who received a botulinum toxin injection within 16 weeks before enrolment will be excluded. * Insufficient motor control to move the avatar on the screen. * Concurrent enrolment in another investigational study. * Pregnancy (self reported).
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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 of Exeter
Exeter, EX1 2LU, United Kingdom
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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