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Efficacy of Repetitive Transcranial Magnetic Stimulation Combined with Virtual Reality Scenario Training in Patients with Post-Stroke Dysphagia

Efficacy of Repetitive Transcranial Magnetic Stimulation Combined with Virtual Reality Scenario Training in Patients with Post-Stroke Dysphagia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120665
Enrollment
Unknown
Registered
2026-03-18
Start date
2025-06-20
Completion date
Unknown
Last updated
2026-03-23

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

Conditions

Post-stroke dysphagia (PSD)

Interventions

Group A:On the basis of conventional therapy (including active/passive orofacial muscle training, ice stimulation training, acupuncture, and low-frequency electrical stimulation for swallowing), patie
Group B:On the basis of conventional therapy (including active/passive orofacial muscle training, ice stimulation training, acupuncture, and low-frequency electrical stimulation for swallowing), patie
Group C:On the basis of conventional therapy (including active/passive orofacial muscle training, ice stimulation training, acupuncture, and low-frequency electrical stimulation for swallowing), patie

Sponsors

Affiliated Hospital of Hebei University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
38 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients with post-stroke dysphagia, disease duration of 1–2 months, aged between 38 and 80 years, with a Kubota Water Swallowing Test grade of 4–5; confirmed by cranial CT or MRI without skull defect; and an expected length of hospital stay of >=28 days.

Exclusion criteria

Exclusion criteria: Dysphagia caused by other conditions (such as traumatic brain injury, stroke, etc.); presence of metal implants in the body; structural abnormalities of the swallowing organs; severe diseases of vital organs (e.g., heart, liver, lungs) or malignant tumors; and history of epileptic seizures.

Design outcomes

Primary

MeasureTime frame
Videofluoroscopic Swallowing Study,VFSS;Surface electromyography,sEMG;Resting-state functional Magnetic Resonance Imaging, rs-fMRI;

Secondary

MeasureTime frame
Water Swallowing Test;Volume-Viscosity Swallow Test Assessment;

Countries

China

Contacts

Public ContactLiang Qin

Affiliated Hospital of Hebei University

ygt1907@126.com+86 150 3022 8082

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 3, 2026