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Bedside touchscreen aims to help stroke patients swallow safely

NCT ID NCT07810374

Symptom relief Sponsor: Mei-Yu Lin Source: ClinicalTrials.gov ↗

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 This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Sep 09, 2026 · Last updated Sep 10, 2026 · Updated 1 time

Summary

Researchers are testing whether an interactive bedside education system helps stroke patients with dysphagia, or trouble swallowing, improve their swallowing and quality of life. The trial enrolls 100 adults aged 20 to 75 who are clinically stable within 48 hours of hospital admission for ischemic or hemorrhagic stroke. Participants receive either the interactive system plus routine dysphagia education or routine education alone, and those in the interactive group can use the bedside system for 48 hours. The study measures changes in swallowing difficulty using a 10-item patient questionnaire and tracks quality of life.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
an interactive bedside dysphagia education system
What this could lead to
If it works, this could give stroke patients with swallowing trouble a simple bedside tool that adds to standard education and may help them swallow better and feel better day to day.
What could go wrong
This is a small, single-center study of 100 people, and an education tool may not change swallowing biology. Any gains could come from extra attention rather than the system itself, and results may not hold for patients with severe aphasia or unstable stroke.

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

About 100 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Jun 2027

An estimate. End dates often move.

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

20 to 75 years

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: 1. Patients diagnosed with ischemic or hemorrhagic stroke and dysphagia. 2. Aged 20-75 years. 3. Clinically stable and within 48 hours of admission to the inpatient ward. Exclusion Criteria: 1. Impaired consciousness or clinically unstable condition. 2. Moderate to severe aphasia that prevents completion of the study procedures. 3. Unable to understand the study information or complete the required assessments. 4. Unable to complete all scheduled assessment time points.

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Conditions

The condition(s) this trial relates to.

Deglutition Disorders

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Dysphagia following cerebrovascular accident

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  3. 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

  • Hospital

    Yuli, Yilan County, 265, Taiwan

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