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Therapeutic Efficacy of Combined Action Observation Therapy and Electromyographic Biofeedback Therapy in Post-Stroke Dysphagia Patients

Therapeutic Efficacy of Combined Action Observation Therapy and Electromyographic Biofeedback Therapy in Post-Stroke Dysphagia Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106969
Enrollment
Unknown
Registered
2025-08-01
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Interventions

Control Group:Basic Swallowing Training + Sham Action Observation Therapy (AOT) + Sham Electromyographic Biofeedback (EMG-BFB)
Observation Group 1 (Control Intervention Group):Basic Swallowing Training + Sham Action Observation Therapy (AOT) + Active Electromyographic Biofeedback (EMG-BFB)
Observation Group 2 (Active AOT Control Group):Basic Swallowing Training + Active Action Observation Therapy (AOT) + Sham Electromyographic Biofeedback (EMG-BFB)
Observation Group 3 (Combined Intervention Group):Basic Swallowing Training + Active Action Observation Therapy (AOT) + Active Electromyographic Biofeedback (EMG-BFB)

Sponsors

Affiliated Hospital of Chengdu University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Clinical diagnosis of cerebral infarction or cerebral hemorrhage, confirmed by head CT or MRI; 2. Surface electromyography test confirmed the presence of swallowing disorders; 3. Initial onset, 2 weeks ~ 6 months of disease, lesion in cerebral hemisphere; 4. Clear consciousness and stable condition; 5. Drinking water test in depression >=3 level; 6. Patients with good cognition, who can understand and cooperate with instructions; 7. No obvious abnormalities in hearing and vision (or corrected vision); 8. Patients and their families are informed of the study and agree to participate in the study in writing.

Exclusion criteria

Exclusion criteria: 1. Those who have a history of other serious physical diseases and various mental illnesses and cannot cooperate with various examinations; 2. Patients with malignant tumors (cranial lesions caused by cranial malignant tumors, metastases, etc.); 3. Those with severe cognitive impairment and aphasia; 4. Those who have poor compliance and cannot cooperate with examination and treatment; 5. The lesion is located in the brainstem; 6. History of laryngeal neck surgery or metal internal fixation.

Design outcomes

Primary

MeasureTime frame
Surface EMG test;Standard Swallowing Function Rating Scale score;

Secondary

MeasureTime frame
Drinking water test in low-lying areas;Swallowing-specific quality of life scale score;Functional Oral Feeding Scale score;

Countries

China

Contacts

Public ContactYang He

Affiliated Hospital of Chengdu University of Traditional Chinese Medicine

971274159@qq.com+86 136 4808 5638

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026