Virtual reality or electrical stimulation: which boosts stroke arm recovery?
NCT ID NCT07666308
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether adding virtual reality-based mirror therapy or electrical stimulation-assisted cycling to standard rehab helps stroke survivors regain arm function better than rehab alone. Sixty adults who had a stroke within the past six months took part in a four-week program. Researchers measured arm movement, daily use, and quality of life before and after treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- virtual reality-based mirror therapy and functional electrical stimulation-assisted cycling
- What this could lead to
- If successful, this could point toward effective rehabilitation strategies to improve arm function and quality of life after stroke.
- What could go wrong
- This is a small, completed trial with 60 participants. Results may not apply to all stroke survivors, and the therapies may not outperform standard rehabilitation.
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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60 people
The number who actually took part.
- Started
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May 2021
- Finished
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Feb 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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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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age older than 18 years * First-ever stroke * Unilateral hemiplegia * Time since stroke onset ≤6 months * Upper extremity Brunnstrom recovery stage between 1 and 4 * Modified Ashworth Scale score \<3 in the affected upper extremity * Ability to maintain sufficient sitting balance Exclusion Criteria: * Visual impairment * Contraindication to electrical stimulation, including cardiac pacemaker implantation * Cognitive impairment (Mini-Mental State Examination score \<25) * Severe aphasia preventing completion of clinical assessments * Presence of additional neurological disorders, including Parkinson's disease, Alzheimer's disease, multiple sclerosis, neuromuscular junction disorders, motor neuron disease, or peripheral nerve lesions * Neglect syndrome * Orthopedic conditions affecting upper extremity function, including amputation or joint contracture * Severe cardiac disease * Uncontrolled hypertension * Epilepsy * Psychiatric disorders such as schizophrenia or bipolar disorder * Pregnancy or suspected pregnancy * Acute deep vein thrombosis or thrombophlebitis * Local infection at the treatment site
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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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Ankara Bilkent City Hospital, Physical Medicine and Rehabilitation Hospital
Ankara, Ankara, 06800, Turkey (Türkiye)
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