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Effects of inspiratory muscle training on patients with dysphagia and aspiration after ischemic stroke

Effects of inspiratory muscle training on patients with dysphagia and aspiration after stroke

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088228
Enrollment
Unknown
Registered
2024-08-13
Start date
2023-01-13
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Dysphagia and aspiration

Interventions

Treatment group:Conventional swallowing training combined with inspiratory muscle training
Control group:Routine swallowing function training: oral sensory training and oral motor organ training, airway safety protection training, Mendelsohn maneuver and neuromuscular electrical stimulation

Sponsors

Nanping First Hospital Affiliated to Fujian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
33 Years to 76 Years

Inclusion criteria

Inclusion criteria: (1) meet the diagnostic criteria of stroke in the "Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke 2018" and combined with swallowing dysfunction; (2) The first onset, the course of disease was 48 hours or 1 month after the condition was stable; (3) The preliminary screening test of Kubota drinking water was above grade 3; (4) aged 18-80 years old; Patients who are able to cooperate; (5) Penetration-aspiration scale (PAS) = 6; (6) Patients or their family members agreed to accept the study and swallow radiography and other examinations, and signed informed consent before the study.

Exclusion criteria

Exclusion criteria: (1) age > 80 or < 18 years old; (2) those with severe mental disorders; (3) patients with a history of cerebral infarction and dysphagia; (4) patients with severe liver and kidney diseases; (5) patients with chronic obstructive pulmonary disease; (6) unstable myocardial infarction, arrhythmia, coronary heart disease and other heart diseases; (7) Grand mal seizures requiring drug therapy; (8) patients with aortic aneurysm; (9) the elderly, frail patients, patients who cannot use neuromuscular electrical stimulation, such as bleeding tendency, acute inflammation, local skin ulceration, local metal implantation, cardiac pacemaker installation, and patients with severe heart disease; (10) Unable to complete the study or withdrawing from the study due to various reasons. This study was approved by the Medical Ethics Committee of our hospital.

Design outcomes

Primary

MeasureTime frame
penetration-aspiration scale (PAS) based on Video fluoroscopic swallowing study (VFSS);

Secondary

MeasureTime frame
Functional Dysphagia Scale (FDS) and Functional Oral Intake Scale (FOIS) based on Video Fluoroscopic Swallowing Study (VFSS);Maximal peak expiratory flow rate (PEF), Forced vital capacity (FVC);

Countries

China

Contacts

Public Contactliu shan

Nanping First Hospital Affiliated to Fujian Medical University

421002703@qq.com+86 183 9658 7187

Outcome results

None listed

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