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The effect of repetitive transcranial magnetic stimulation combined with peripheral magnetic stimulation on post-stroke dysphagia

The effect of repetitive transcranial magnetic stimulation combined with peripheral magnetic stimulation on post-stroke dysphagia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105062
Enrollment
Unknown
Registered
2025-06-27
Start date
2025-06-30
Completion date
Unknown
Last updated
2025-06-30

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

Conditions

Dysphagia after stroke

Interventions

Peripheral magnetic stimulation treatment group:Conventional swallowing rehabilitation training + high-frequency rPMS of the infrahyoid muscles
Transcranial magnetic stimulation treatment group:Conventional swallowing rehabilitation training + high-frequency rTMS of the orolingual cortex
Transcranial Magnetic Stimulation-Peripheral Magnetic Stimulation Combined Treatment Group:Conventional swallowing rehabilitation training + high-frequency rPMS of the infrahyoid muscles+high-frequenc

Sponsors

The Affiliated Rehabilitation Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Meet the diagnostic criteria for stroke as established by the 4th National Cerebrovascular Disease Academic Conference and confirmed by cranial CT or MRI scans; 2.The stroke is the first onset, and the course of the disease is within half a year; 3.Adults (18-80 years old) with dysphagia after stroke; 4.Conscious with stable vital signs; 5.Able to understand and execute physician's instructions; 6.The Kubota Water Swallowing Test was positive, and a GUSS swallowing function assessment was conducted. A fiberoptic endoscopic evaluation of swallowing (FEES) confirmed the presence of swallowing dysfunction; 7.The patient or their family members agreed to participate in this study and undergo a laryngeal endoscopy swallowing evaluation. Informed consent was obtained prior to the study;

Exclusion criteria

Exclusion criteria: 1.Refuse to cooperate with the inspection; 2.Insufficient function of vital organs such as the heart, lungs, and kidneys; 3.Severe brain hemorrhage, brain trauma, tumors, infections, and other diseases that may trigger epilepsy. 4.Acute large-area cerebral infarction, multiple intracranial aneurysms; 5.Severe or recent heart attack; 6.High-frequency and high-intensity transcranial magnetic stimulation (TMS) is contraindicated in individuals with a history of epilepsy or those showing epileptiform abnormalities on EEG; 7.Contraindications for magnetic stimulation therapy include (but are not limited to): implanted electronic devices/intracranial metal devices; history of head and neck cancer or oral cancer surgery, or other structural lesions in the head and neck region; 8.glaucoma, retinal detachment; 9.Suffering from other serious diseases that affect swallowing (such as cancer, chronic respiratory diseases, etc.); 10.pregnant woman;

Design outcomes

Primary

MeasureTime frame
Electromyographic (EMG) signals from the suprahyoid muscles;Assessment of bolus transit during swallowing and detection of any residual food retention.;

Secondary

MeasureTime frame
Grading of laryngeal penetration/aspiration;Ability for oral alimentation;

Countries

China

Contacts

Public ContactLiu Chang

The Affiliated Rehabilitation Hospital of Chongqing Medical University

351745691@qq.com+86 18623012626

Outcome results

None listed

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