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Effect of Different Intensities of Inspiratory Muscle Training on Cardiac Function in Non-Ambulatory Stroke Patients: A Clinical Study

Effect of Different Intensities of Inspiratory Muscle Training on Cardiac Function in Non-Ambulatory Stroke Patients: A Clinical Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116974
Enrollment
Unknown
Registered
2026-01-18
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Stroke

Interventions

High-Intensity Inspiratory Muscle Training Group:Conventional training combined with High-intensity inspiratory muscle training
Moderate-intensity inspiratory muscle training group:Conventional training combined with moderate-intensity inspiratory muscle training

Sponsors

Shenzhen Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed with cerebral infarction or intracerebral hemorrhage according to the 2019 Chinese Guidelines for Diagnosis of Major Cerebrovascular Diseases, confirmed by cranial CT or MRI; 2. Age 40 17 for illiterate, >20 for primary school education, >24 for junior high school or higher; able to comply with treatment and assessments; 7. Willing to participate and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with unstable vital signs, consciousness, or laboratory indicators; 2. Acute myocardial infarction or acute heart failure, uncontrolled hypertension, arrhythmia, or unstable cardiovascular conditions; 3. Patients who have taken medications affecting the respiratory system within the past month; 4. Patients with respiratory diseases (such as chronic obstructive pulmonary disease, asthma, cystic fibrosis, etc.), heart failure, myasthenia gravis, or other conditions that may impair respiratory muscles; 5. Patients with nasogastric tubes, endotracheal intubation, or any situation that interferes with measurement or implementation of the research protocol; 6. Patients with House-Brackmann grade III or higher facial paralysis, making it impossible to ensure the effectiveness of respiratory training.

Design outcomes

Primary

MeasureTime frame
Stroke volume;

Secondary

MeasureTime frame
End-diastolic volume;Systemic vascular resistance;Heart rate;Long's Activities of Daily Living Assessment Scale;Blood oxygen saturation;Forced expiratory volume in one second;Forced vital capacity;Maximal inspiratory pressure;Cardiac output;

Countries

China

Contacts

Public ContactWang Yulong

Shenzhen Second People's Hospital

345399075@qq.com+86 755 83366388

Outcome results

None listed

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