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Efficacy of Precise Magnetoelectric Regulation Based on Motor Evoked Potentials for Dysphagia in Children with Brain Injury

Efficacy of Precise Magnetoelectric Regulation Based on Motor Evoked Potentials for Dysphagia in Children with Brain Injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124216
Enrollment
Unknown
Registered
2026-05-08
Start date
2026-05-25
Completion date
Unknown
Last updated
2026-05-11

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

Conditions

Dysphagia in children after brain injury

Interventions

Experimental group 2:Swallowing training+rTMS targeted by MEP+Vitalstim electrical stimulation
Experimental group 1:Swallowing training+rTMS targeted by MEP

Sponsors

Shanghai Yangzhi rehabilitation hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 16 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for brain injury (diagnostic criteria refer to Liu Zhenhuan's edited book 'Atlas of Rehabilitation Training for Children with Motor Development Delay'): (1) Presence of high-risk factors such as jaundice, hypoxic-ischemic cerebral injury, or brain injury; (2) Infants and young children with a developmental quotient (DQ) < 85; (3) Reduced or increased muscle tone; (4) Delay in developmental milestones; 2. Age between 3 and 16 years; 3. First diagnosis of brain injury with dysphagia, disease course 2~8 weeks, conscious, and stable vital signs; 4. Swallowing imaging indicates dysphagia; 5. No history of epilepsy, severe neurological diseases, or other psychiatric history; 6. No exposure to other neuromodulation treatments in the past 30 days; 7. Informed consent obtained from the patient and family.

Exclusion criteria

Exclusion criteria: 1. Dysphagia caused by previous or comorbid diseases 2. People with a history of epilepsy, intracranial metal implants, pacemakers, or coronary stents; those with skull defects; patients with heart failure or severe liver and kidney dysfunction; patients with mental illnesses; patients who cannot cooperate due to severe aphasia or dementia; patients with cricopharyngeal muscle relaxation disorders. 3. Those who do not cooperate with treatment; 4. Others whom the researchers judge to be unsuitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
The change in Functional Oral Intake Scale (FOIS) score from baseline;

Secondary

MeasureTime frame
Change in PAS score from baseline;Amplitude changes in suprahyoid/tongue surface electromyography (sEMG);

Countries

China

Contacts

Public ContactWu Yanqiu

Shanghai Yangzhi rehabilitation hospital

13661854517@163.com+86 21 3773001

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 16, 2026