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A Study on the Application of Respiratory Muscle Resistance Training in Post-Stroke Patients with Dysphagia

A Study on the Application of Respiratory Muscle Resistance Training in Post-Stroke Patients with Dysphagia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104698
Enrollment
Unknown
Registered
2025-06-20
Start date
2025-06-30
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Dysphagia after stroke

Interventions

control group:Control group: Routine neurosurgical nursing care + swallowing function training Referring to the "Chinese Guidelines for the Prevention and Treatment of Cerebrovascular Disease," the cl
Respirator

Sponsors

Huzhou First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria of the 2014 Chinese Guidelines for the Diagnosis and Treatment of Acute Stroke, confirmed by cranial CT or MRI. 2.A score of Grade 3 or above on the Water Swallowing Test, with swallowing dysfunction demonstrated by videofluoroscopic swallowing study (VFSS) 3. Age between 18 and 65 years old. 4. First-time onset of stroke, with stable condition after 48 hours. 5. There are no cognitive impairments, such as aphasia, auditory comprehension disorders, attention impairments, and perceptual impairments. 6. Conscious and cooperative patients without impaired consciousness. 7. Consent obtained from the patient and their family, with signed informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients exhibiting disease progression with radiologically confirmed new cerebral infarction or hemorrhagic lesions; (2) Individuals with a history of prior respiratory muscle training; (3) Presence of severe primary cardiac, hepatic, pulmonary, renal, or hematological diseases, or other life-threatening comorbidities; (4) Patients with documented psychiatric history or psychoactive substance abuse disorders; (5) Subjects unwilling to comply with trial protocols and voluntarily refusing to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
swallowing function;

Secondary

MeasureTime frame
Respiratory Muscle Function;Pulmonary Function;incidence of aspiration pneumonia;

Countries

China

Contacts

Public ContactLiying Dong

The First People’s Hospital of Huzhou, Zhejiang, China

zhongxingming@126.com+86 138 6728 6288

Outcome results

None listed

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