None listed
Conditions
Interventions
Medical Device : The subjects of the study are divided into two groups by a random number table, and the control group and the experimental group are tested without electrical stimulation during the s
Sponsors
Seoul National University Bundang Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients with confirmed oropharyngeal dysphagia on VFSS Patients who clinically need to apply electrical stimulation therapy for dysphagia due to oropharyngeal dysphagia caused by central nervous system disease Patients over 19 years of age regardless of gender A person who voluntarily agrees to the clinical trial and is able to visit for the next observation Patients with dysphagia within six months of developing dysphagia (including patients with dysphagia caused by stroke, traumatic brain injury, cervical injury, etc.)
Exclusion criteria
Exclusion criteria: Refusing to inspect If you don't agree Where it is impossible to perform instructions due to mental illness, etc A person who has dysphagia caused by respiratory failure, cervical surgery, head and neck surgery, chemical and radiotherapy of the neck, etc Pregnant women and nursing mothers Pre-interviews are conducted only for women of childbearing age to determine whether they are pregnant and breastfeeding. If the pregnancy status is confirmed through a photo interview, it is excluded from the test. If the pregnancy status is uncertain or suspected, it is confirmed through a urine test, and participation in the study only when pregnancy is excluded. Patients who fail to apply electrical stimulation therapy due to allergies, hypersensitivity reactions, etc Other persons who have comorbidities (e.g., malignant tumors, severe renal/liver/lung disease, blood clotting abnormalities, etc.) that are not suitable for participation in the clinical trial as judged by the researcher A person equipped with a pacemaker and other electrical stimulators in the body A person who is participating in another clinical trial at the time of screening Other persons deemed unsuitable for this clinical trial by the researcher
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of VDS total change after two weeks of intervention with the results of the video-toothed swallowing test between the experimental group and the control group | — |
Secondary
| Measure | Time frame |
|---|---|
| ? Comparison of the change amount of the VDS (oral score) using the results of the video projection swallowing test ? Comparison of the change amount of the pharyngeal score (VDS) using the results of the video projection swallowing test ? Comparison of the change value of the penetration aspiration scale (PAS) using the results of the video projection swallowing test between the experimental group and the control group ? Comparison of the change value of the functional intake scale (FOIS) between the experimental group and the control group ? Comparison of the change value of the quality of life (M.D. and person dysphagia inventory) after application of the four-channel electrical stimulation therapy between the experimental group and the control group ? Comparison of the change value of the electrical stimulation satisfaction, ease of swallowing, and discomfort after application of the four-channel electrical stimulation therapy group ? Comparison of the change value of the Tongue Strength through the IOPI Comparison ? of the change value of the body composition through the Bioelectric Impedance Analysis Analysis (BIA) Comparison of the MNA-SF and the change value of the body composition through the MNA-SF in dysphagia patients with dysphagia (InBody) Comparison of the variation values of oral intake | — |
Countries
Korea, Republic of
Contacts
Public ContactRyu juseok
Seoul National University Bundang Hospital
Outcome results
None listed