NCT07810374Enrolling by invitation
Evaluation of Effectiveness of an Interactive Dysphagia Education System for Patients With Stroke
Development and Evaluation of Effectiveness of an Interactive Dysphagia Education System for Patients With Stroke
Source: ClinicalTrials.gov · Last updated 9 Sept 2026
Brief summary (registry, in English)
The goal of this clinical trial is to learn if an interactive dysphagia education system can improve swallowing outcomes and quality of life in patients with post-stroke dysphagia. The main questions it aims to answer are: Does the interactive dysphagia education system improve swallowing outcomes? Does the interactive dysphagia education system improve quality of life? Researchers will compare the interactive dysphagia education system plus routine dysphagia education with routine dysphagia education alone to see if the interactive system provides additional benefits. Participants will: Receive either interactive dysphagia education plus routine education or routine education alone Use the interactive dysphagia education system at the bedside for 48 hours if assigned to the interactive education group Complete assessments of swallowing outcomes and quality of life
- Status (registry)
- Enrolling by invitation
- Study type
- Interventional
- Enrollment
- 100 (estimated)
- First submitted
- 3 Sept 2026
- Start date
- 1 Sept 2026
- Primary completion date
- 22 Jun 2027
- Lead sponsor
- Mei-Yu Lin
- Diseases
- Stroke
- NCT number
- NCT07810374
What you commit to
- Study type: Interventional
- Planned participants: 100
- From 1 Sept 2026 to the primary completion date, 22 Jun 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Impaired consciousness or clinically unstable condition.
Other
- Moderate to severe aphasia that prevents completion of the study procedures.
- Unable to understand the study information or complete the required assessments.
- Unable to complete all scheduled assessment time points.
Who the study is looking for
- Patients diagnosed with ischemic or hemorrhagic stroke and dysphagia.
- Aged 20-75 years.
- Clinically stable and within 48 hours of admission to the inpatient ward.
Age in the registry: 20 years to 75 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Hospital Coordinator of this site? Confirm its status | Yuli | Taiwan | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.