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The effect of extracorporeal counterpulsation technology combined with inspiratory muscle training on the cardiac and pulmonary functions of stroke patients

The effect of extracorporeal counterpulsation technology combined with inspiratory muscle training on the cardiac and pulmonary functions of stroke patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119351
Enrollment
Unknown
Registered
2026-02-26
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Stroke

Interventions

EECP plus IMT Group (Combined Group):Conventional stroke medication, respiratory training, and limb function rehabilitation + IMT (POWERbreathe K5 inspiratory muscle trainer, intensity 30%-50% MIP) +
once daily, 5 times per week for 4 weeks
IMT Group:Conventional stroke medication, respiratory training, and limb function rehabilitation + IMT (POWERbreathe K5 inspiratory muscle trainer, intensity 30%-50% MIP)
Control Group:Conventional stroke medication, respiratory training, and limb function rehabilitation

Sponsors

Beijing Xiaotangshan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. The patient's diagnosis meets the criteria for stroke. The results of head CT or MRI examinations can clearly confirm that the selected subjects are patients with ischemic stroke. The patient must have been diagnosed for the first time and the duration of the disease should be no more than 6 months. 2. Age: 40 - 75 years old. 3. Stable vital signs, without speech or cognitive function disorders. 4. Able to cooperate with the completion of respiratory training. 5. The patient's clinical data is complete and the informed consent form has been signed.

Exclusion criteria

Exclusion criteria: 1. History of lung and thoracic-abdominal diseases; 2. Complicated with myasthenia gravis or diaphragmatic nerve paralysis; 3. Having a history of malignant tumors or serious diseases of important organs such as the heart, liver, and kidneys; 4. The patient has brainstem infarction; 5. There is a cardiac pacemaker or other metal implants in the body; 6. Pregnant or lactating women; 7. Patients with a history of epilepsy; 8. Those whose conditions prevent them from cooperating with treatment for other reasons.

Design outcomes

Primary

MeasureTime frame
Six-Minute Walk Test (6MWT);Safety Outcomes (including adverse events, serious adverse events, new lesions, deterioration of existing symptoms or signs, worsening of concomitant diseases, lower limb edema, muscle soreness, bruising, blood pressure fluctuations, etc.);

Secondary

MeasureTime frame
Left Ventricular Ejection Fraction (LVEF);Left Ventricular End-Systolic Diameter (LVESD);Left Ventricular End-Diastolic Diameter (LVEDD);Forced Vital Capacity (FVC);Forced Expiratory Volume in the First Second (FEV1);Maximum Voluntary Ventilation (MVV);Maximal Inspiratory Pressure (MIP);Peak Expiratory Flow (PEF);

Countries

China

Contacts

Public ContactLiu Mingyue

Beijing Xiaotangshan Hospital

lmyxts0508@163.com+86 152 1005 0860

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026