Stroke rehabilitation with innovative extended reality (STRIVE): a feasibility study in clinical practice
NCT ID NCT07811440
First seen Sep 10, 2026 · Last updated Sep 10, 2026
Summary
After a stroke, many people experience difficulties with movement, balance, or everyday activities. Rehabilitation is an important part of recovery and can help people regain function and confidence in daily life. However, rehabilitation can sometimes become repetitive, tiring, or difficult to maintain over time. This research project studies the use of Mixed Reality (MR) in stroke rehabilitation. MR uses special glasses that project digital holograms into the real-world environment. This allows individuals to see and interact with virtual objects while remaining aware of and moving within their actual surroundings. Using MR, people can practice movements and functional activities in a safe, engaging, and interactive way. The holographic exercises can be repeated many times in a structured manner, which is important for recovery after stroke. At the same time, the training can be varied to reduce monotony and maintain motivation. The exercises can be individually adapted to each person's abilities, rehabilitation goals, and daily condition. The level of difficulty can be adjusted as the person progresses. MR systems can also provide immediate visual and auditory feedback, helping individuals understand their performance and encouraging active participation in their rehabilitation. The project also focuses on how patients experience this type of training and how it fits into everyday life.
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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 9 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2027
An estimate. Start dates often move.
- Expected to finish
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Sep 2028
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
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: * Adults (≥ 18 years) with a verified stroke diagnosis at least six months ago * Sufficient cognitive ability MMES (mini mental state examination) ≥ 23 * Continued need for rehabilitation * Ability to walk at least 10 meters, with or without aids * Be able to read, understand and express themselves in the Swedish language. Exclusion Criteria: * • Serious vision problems that would affect the use of XR equipment * Other progressive or serious illness such as multiple sclerosis, Parkinson's disease, dementia or cancer * People with epilepsy or pacemakers
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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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Rehabilitation Unit, Torsby Hospital
Torsby, Värmland County, Sweden
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Health, functioning, work, and experiences of social and health services of persons with stroke
- Insights into impaired arm motor control on bilateral and unilateral functional activities after injury: a kinematic study
- Emergency stroke unit for acute cerebrovascular events: a prospective, single-arm trial with a historical control group
- 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