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Can a touch screen help stroke patients see better?

NCT ID NCT04930822

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

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

37 people

The number who actually took part.

Started

Jan 2021

Finished

Sep 2024

Lead sponsor

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

18 years and older

Sex

Anyone

Healthy volunteers

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

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

  • Gaylord Hospital

    Wallingford, Connecticut, 06492, United States

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