None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ? Patients diagnosed with post-stroke dysphagia ? Patients who are capable of oral intake or are scheduled to initiate an oral diet ? Patients who understand the purpose and procedures of the study and voluntarily provide written informed consent
Exclusion criteria
Exclusion criteria: ? Patients with ongoing aspiration pneumonia or acute lung disease upon admission, or those for whom evaluation and protocol interventions are difficult due to decreased consciousness or systemic instability ? Patients with moderate-to-severe cognitive impairment (MMSE score of 18 or below) or severe communication barriers that make it difficult to understand the study explanation, complete assessment tools, or participate in protocol interventions ? Patients who are unable to take oral intake and have no plans to initiate an oral diet during the study period ? Patients for whom follow-up is difficult due to scheduled transfer, discharge, or changes in the treatment plan during the study period ? Patients judged to have difficulty completing the study procedures due to severe fatigue, general weakness, repeated medical procedures, or lack of cooperation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.GUSS (Gugging Swallowing Screen) 2.Protocol Feasibility | — |
Secondary
| Measure | Time frame |
|---|---|
| Dysphagia Symptoms (K-EAT-10) ;Protocol Content Validity and Applicability;Oral Assessment Tool(Revised Oral Assessment Guide) | — |
Countries
Korea, Republic of
Contacts
Gwangju 365 Rehabilitation Hospital