Skip to content

Analysis of the Efficacy of Repetitive Peripheral Magnetic Stimulation (rPMS) Combined with Repetitive Transcranial Magnetic Stimulation (rTMS) on Swallowing Disorders in Stroke Patients

Analysis of the Efficacy of Repetitive Peripheral Magnetic Stimulation (rPMS) Combined with Repetitive Transcranial Magnetic Stimulation (rTMS) on Swallowing Disorders in Stroke Patients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091587
Enrollment
Unknown
Registered
2024-10-30
Start date
2024-10-30
Completion date
Unknown
Last updated
2024-11-04

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

Conditions

Dysphagia after stroke

Interventions

Sponsors

Department of Rehabilitation Medicine, Second Affiliated Hospital of Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1: Meets the stroke diagnosis criteria established by the 4th National Academic Conference on Cerebrovascular Diseases and confirmed by cranial CT or MRI scans. 2: First stroke, with a duration of illness between 7 days to 6 months. 3: Age between 40 and 85 years. 4: Conscious, stable vital signs. 5: Able to understand and follow the study-related instructions. 6: Positive result from the drinking water test, with swallowing difficulties confirmed by videofluoroscopic swallowing study (VFSS). 7: Right-handed. 8: Patient or family member consents to participate in this study and undergo videofluoroscopic swallowing study, signing an informed consent form before the study.

Exclusion criteria

Exclusion criteria: 1: Dysfunction of important organs such as the heart, lungs, and kidneys. 2: Recent epilepsy seizures. 3: Presence of swallowing difficulties caused by other neurological diseases or structural abnormalities or injuries in the head and neck. 4: Presence of contraindications for magnetic stimulation. 5: Other circumstances deemed unsuitable for inclusion by researchers.

Design outcomes

Primary

MeasureTime frame
PAS scale;DOSS scale;FOIS scale;parameters of VFSS;

Secondary

MeasureTime frame
swallowing quality of life;

Countries

China

Contacts

Public ContactQiaojun Zhang

Second Affiliated Hospital of Xi'an Jiaotong University, Department of Rehabilitation Medicine

zhangqj@mail.xjtu.edu.cn+86 138 9186 7155

Outcome results

None listed

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