None listed
Conditions
Interventions
Medical Device : Patients who agree to participate in the study are randomly assigned to either the NMMS group or the NMES group. Once assigned to each group, subjects will receive total ten of 30-min
of the intensity at which the patient begins to experience local pain
Duration : 2 sec stimulation, 28 sec rest, for 10 min duration (total 1200 pulse)
Stimulation site : suprahyoid muscle gro
Sponsors
Chungnam National University Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Adult patients over 19 years old 2. Diagnosis of stroke by neurologist or neurosurgery using radiologic tools like CT or MRI 3. Airway aspiration of liquid diet confirmed by videofluoroscopic swallowing study (VFSS) within a month after stroke onset 4. Over 1-step cooperation is possible 5. Neck control and sitting is possible 6. No problems with swallowing before stroke onset
Exclusion criteria
Exclusion criteria: 1. History of stroke with a transient ischemic attack or existing clinical symptoms 2. Progressive or unstable stroke 3. Existing serious neurogenic disease 4. Existing severe liver, kidney, heart and respiratory disease 5. Lifespan less than 1 year, because of medical illness
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| American speech-language-hearing association national outcome measurement system swallowing level scale (ASHA-NOMS) | — |
Secondary
| Measure | Time frame |
|---|---|
| Functional dysphagia scale (FDS);Penetration-aspiration scale (PAS);Mylohyoid motor evoked potential (MH-MEP);The Koeran Swallowing-Quality of Life Questionnaire (K-SWAL-QOL) | — |
Countries
Korea, Republic of
Contacts
Public ContactYeong Wook Kim
Chungnam National University Hospital
Outcome results
None listed