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Application of flexible endoscopic video-assisted swallowing therapy in the rehabilitation of post-stroke dysphagia

Application of flexible endoscopic video-assisted swallowing therapy in the rehabilitation of post-stroke dysphagia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300074018
Enrollment
Unknown
Registered
2023-07-27
Start date
2023-07-28
Completion date
Unknown
Last updated
2023-10-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

post-stroke dysphagia

Interventions

control group:routine rehabilitation treatment of swallowing
video group:assisted swallowing therapy (real-time video)
non-video group:assisted swallowing therapy (non-video)

Sponsors

Jiangwan Hospital, Hongkou District of Shanghai
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Adult (18-80 years old) patients who meet the diagnostic criteria for hemorrhagic or ischemic stroke in the "Key Diagnostic Points for Various Major Cerebrovascular Diseases in China 2019" and have been diagnosed with stroke through CT or MRI examination; 2. Dysphagia was found by dysphagia screening and confirmed by flexible endoscopic evaluation of swallowing (FEES); 3. The patient's consciousness is clear and the vital signs are stable; 4. The patients agreed to participate in the study and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Subarachnoid hemorrhage, unabsorbed hematoma of cerebral hemorrhage, progressive stroke; 2. Patients with a history of epilepsy; 3. Patients with serious diseases of heart, liver, lung, kidney and other important organs or mental disorders who do not cooperate with examination and treatment; 4. Patients with other diseases of nervous system or otorhinolaryngology that affect swallowing function; 5. Patients with cognitive impairment: the total score of montreal cognitive assessment-basic(MoCA-B) was less than 24 points; 6. Patients with serious hearing comprehension disorders; 7. Patients with clinically significant visual or hearing impairments.

Design outcomes

Primary

MeasureTime frame
Standardized Swallowing Assessment (SSA) ;Fiberoptic Endoscopic Dysphagia Severity Scale (FEDSS);Penetration-Aspiration Scale (PAS);swallowing quality-of-life questionnaire (SWAL-QOL);

Countries

China

Contacts

Public ContactMa Huizhi

Jiangwan Hospital, Hongkou District of Shanghai

huizhi8011@163.com+86 158 0068 1719

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026