dysphagia
Conditions
Interventions
Experimental group:Pharyngeal sensory electrical stimulation
Control group:False pharyngeal sensory electrical stimulation
Sponsors
The Third Affiliated Hospital of Sun Yat-Sen University
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Patients aged 18 to 80 years who are hospitalized with central nervous system diseases such as cerebral infarction, cerebral hemorrhage, and traumatic brain injury; 2. FOIS score 1-2; 3. The vital signs are stable, and there is no serious heart or lung disease; 4. There was no significant improvement in swallowing function after 1 month of routine swallowing rehabilitation; 5. There is no hearing comprehension disorder, and the treatment can be cooperated; 6. The patient or legal representative signed the informed consent.
Exclusion criteria
Exclusion criteria: 1. Severe cognitive impairment (MMSE <13 points), severe aphasia; 2. Vocal cord tremor, spasm, and significantly limited abduction; 3. Pacemaker or implantable cardiac defibrillator, unstable cardiopulmonary status, severe arrhythmia, etc.; 4. Oropharyngeal anatomical structure distortion, head and neck tumors; 5. Combined with esophageal perforation, esophageal stenosis, esophageal diverticulum, gastric ulcer bleeding, esophageal varices; 6. Patients who cannot cooperate with the evaluation of FEES, HRM, VFSS, fNIRs, etc.; 7. Women who are pregnant, planning to become pregnant or breastfeeding.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| functional oral food intake scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| Leakage Aspiration Score;Murry secretion scale;Yale residue classification scale;Hypopharyngeal peak pressure; | — |
Countries
China
Contacts
Public ContactWen Hongmei
The Third Affiliated Hospital of Sun Yat-Sen University
Outcome results
None listed