Post-stroke dysarthria
Conditions
Interventions
Control group:Pseudo-ASP-articulation task (10min) + conventional dysarthria rehabilitation training
Experimental group:ASP - articulation task (10min) + regular dysarthria rehabilitation training
Sponsors
Tongji Hospital Affiliated to Tongji Medical College, Huazhong University of Science and Technology
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: 1. Age from 18 to 80 years old, male or female; 2. Patients who met the diagnostic criteria of stroke (first stroke confirmed by clinical CT or MRI) were conscious, with stable vital signs, and the course of stroke was from 2 weeks to 6 months. 3. Mild to moderate dysarthria was assessed by Frenchay rating scale. 4. Native speaker of Chinese, can communicate in putonghua in daily life before onset, primary school or above diploma 5. No history of hearing impairment and good tolerance to sudden sound stimulation at 114 dB. 6. Sign the informed consent, voluntarily participate in the trial, and be able to complete the trial. 7. The head was intact and no craniotomy and/or skull repair was performed.
Exclusion criteria
Exclusion criteria: Exclusion criteria: 1. The subjects were pregnant, dizzy, poor mental state, epileptic seizures, psychiatric history, and/or complicated with serious cardiovascular, liver and kidney diseases within the past year. 2. A history of other conditions affecting swallowing, speech and/or language, such as dementia, Parkinson's disease or oral cancer; 3. Patients below grade 3 on the BDAE aphasia severity assessment. 4. Patients with severe cognitive impairment assessed by MMSE (MMSE score < 20) 5. Patients with vocal cord paralysis, hearing impairment, and visual impairment were excluded. 6. Exclude those with damage or lesions in organs or muscles involved in articulation. 7. Patients with upper respiratory tract infection, such as cough, hoarseness and other patients who affect voice, were excluded. 8. Patients with skull defects, such as those who underwent surgical treatment such as decompressive craniectomy after stroke, were excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Clinical Scale evaluation; | — |
Secondary
| Measure | Time frame |
|---|---|
| Analysis of acoustic properties;Functional near-infrared spectroscopy; | — |
Countries
China
Contacts
Public ContactLu Min
Tongji Hospital Affiliated to Tongji Medical College, Huazhong University of Science and Technology
Outcome results
None listed