Robot or mirror? new study tests best way to recover arm use after stroke
NCT ID NCT07435688
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested two methods to help people regain arm movement after a stroke: looking at a mirror to trick the brain, or using a robotic hand glove that mimics the healthy arm. Thirty adults who had a stroke within the past year took part. Both groups also received standard physical therapy for six weeks. The goal was to see which approach works better for improving motor function 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
- mirror therapy and robotic hand device
- What this could lead to
- If successful, this could show that robotic mirror therapy is more effective than standard mirror therapy for regaining arm and hand function after a stroke.
- What could go wrong
- This is a small, completed trial with only 30 participants, so results may not apply to all stroke survivors. The interventions are for symptom improvement, not a cure.
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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30 people
The number who actually took part.
- Started
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Jan 2024
- Finished
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Dec 2024
- 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: * Having a ischemic/hemorrhagic stroke diagnosis through MRI and/or CT * Volunteering to enter the study * First ever stroke or no sequeale (mRS 0) * Being in subacute/chronic phase of stroke (between 1st week to 1 year) * Having a adequate sitting balance or able to maintain upright sitting position for 30 minutes * Having a motor deficit in the hand (Brunnstrom hand motor recovery stages 1-4 ) * Having a full range of motion in hand Exclusion Criteria: * Severe Pain (VAS ≥ 8) * Having a neurological or orthopedic problem in hand * Severe spatial hemineglect (NIHSS 11th subscale\> 1) * Spasticity (mAS ≥ 2) * Apraxia * Visual/auditory loss that affects treatment * Unstable Vital Signs
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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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Alkent 2000, 34500 Büyükçekmece/İstanbul
Istanbul, Istanbul, 34500, Turkey (Türkiye)
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Istanbul University- Cerrahpasa
Istanbul, Büyükcekmece, 34500, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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- 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
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