Can a touch screen help stroke patients see better?
NCT ID NCT04930822
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether using a touch screen device (BITS) can improve visual field awareness in people recovering from a stroke or brain injury. 37 adults in inpatient rehab were assigned to either standard pen-and-paper vision exercises or exercises on the BITS touch screen. The goal was to see if the interactive technology leads to better outcomes for vision problems.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Bioness Integrated Therapy System (BITS) touch screen device
- What this could lead to
- If successful, this could offer a more engaging way to help people with vision problems after a stroke or brain injury regain some field awareness.
- What could go wrong
- This is a small, early study with only 37 participants, so results may not apply to everyone. The device is compared to standard exercises, and the improvement 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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37 people
The number who actually took part.
- Started
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Jan 2021
- Finished
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Sep 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: * Adults, 18 years or older who are able to provide consent or have Power of Attorney (POA) able to consent. * Must have an acute or subacute (diagnosed within the last 3 months) neurological diagnosis with a visual field deficit as verified by occupational therapist via confrontation testing. * Admitted for inpatient rehabilitation * Demonstrate the ability to follow 1 step directions * Demonstrate sufficient upper extremity strength (as deemed appropriate by occupational therapist) to utilize BITS touch screen technology * Ability to tolerate at least 30 minutes of intervention at a seated wheelchair level. Exclusion Criteria: * Severe cognitive impairments: Unable to follow one step directions, inability to communicate pain, or to stop intervention if needed * Quadriparesis * Previous significant visual impairment impacting visual fields or resulting in legal blindness in past medical history * Re-admitted to Acute Care and do not return within 1 week * Currently on a ventilator for respiratory support * Unstable vital signs or deemed inappropriate to participate in therapy per Medical Staff * Uncontrolled or new (within 24 hours) arrhythmias. * Unresolved or new (within 24 hours) deep vein thrombosis. * Concurrent severe neurological pathology/disease or stroke within 72 hours. * Any reason the physician may deem as harmful to the participant to enroll or continue in the study.
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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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Gaylord Hospital
Wallingford, Connecticut, 06492, United States
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Other studies related to the condition(s) this trial covers.
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