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Effect of repeated transcranial magnetic stimulation on dysphagia after stroke

Effect of repeated transcranial magnetic stimulation on dysphagia after stroke

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081740
Enrollment
Unknown
Registered
2024-03-11
Start date
2024-03-11
Completion date
Unknown
Last updated
2024-03-18

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

Conditions

Dysphagia after stroke

Interventions

Pre-stimulation group:Pre-stimulation + high-frequency stimulation + conventional swallowing training
Control group:False pre-stimulation + high-frequency stimulation + conventional swallowing training

Sponsors

Shijiazhuang People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Patients who meet the diagnostic criteria revised in the 4th National Conference on Cerebrovascular Diseases, and are confirmed to be stroke patients by head CT or MRI (2) The first onset, aged 25 ~ 60 years old, is a unilateral hemisphere lesion (3) 14 days= course of illness = 6 months (4) The water swallow test (WST) was = grade 2 and met the diagnostic criteria for dysphagia (5) Conscious at the time of admission, with stable vital signs, choking on drinking water, and difficulty swallowing (6) All subjects were approved by patients and their families before enrollment, and informed consent forms were signed

Exclusion criteria

Exclusion criteria: (1) Swallowing disorders caused by other non-stroke diseases, such as head trauma, Parkinson's disease, etc (2) Inability to perform swallowing imaging examination (3) Those with unstable vital signs, serious underlying diseases, and critical condition (4) Coma, severe cognitive dysfunction, severe aphasia, communication disorder, unable to cooperate with assessment and treatment (5) There are contraindications to transcranial magnetic stimulation treatment, such as intracranial metal implants, cardiac pacemakers, epilepsy patients, etc

Design outcomes

Primary

MeasureTime frame
Standard Swallowing Assessment (SSA);

Secondary

MeasureTime frame
Functional Oral Intake Scale (FOIS);Rosenbek Penetration-Aspiration Scale (PAS);Surface electromyography indicators;

Countries

China

Contacts

Public ContactMa Jiang

Shijiazhuang People's Hospital Jianhua District

majiangtutor@sina.com+86 198 3112 5831

Outcome results

None listed

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