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Assessment of bilateral diaphragmatic excursion in stroke hemiplegia rehabilitation patients: comparison of multiple ultrasound measurement indicators

Assessment of bilateral diaphragmatic excursion in stroke hemiplegia rehabilitation patients: comparison of multiple ultrasound measurement indicators

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600118547
Enrollment
Unknown
Registered
2026-02-06
Start date
2026-02-20
Completion date
Unknown
Last updated
2026-02-09

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

Conditions

Stroke with hemiplegia

Interventions

Observation group:None
Control group:None

Sponsors

Hebei General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1 Observation group: 1) Age >= 18 years old; 2) History of stroke, currently in the recovery phase; 3) Stroke resulting in hemiplegia or weakened muscle strength on one side of the limb, and hospitalization for treatment in the rehabilitation department; 4) No obvious abnormal lung diseases were found through pulmonary CT, chest X-ray or pulmonary ultrasound examination; 5) Regularly undergo ultrasound examination and voluntarily participate in the study, cooperate with the examiner to complete diaphragmatic ultrasound examination, and obtain informed consent. 2 Control group: 1) Age >= 18 years old; 2) Good limb muscle strength and motor function; 3) Healthy individuals with heart, lung, and diaphragm related diseases; 4) Voluntarily participate in the study and cooperate with the examiner to complete the diaphragmatic ultrasound examination, and obtain informed consent.

Exclusion criteria

Exclusion criteria: 1 Observation group: 1) Diaphragmatic trauma, intra-abdominal hypertension, and diaphragm dysfunction from other non-stroke etiologies; 2) History of lung, mediastinal, or abdominal surgery; 3) Lung, mediastinal or diaphragmatic tumors; 4) Pregnant women, spinal or chest wall deformities, etc; 5) Moderate to large amounts of pleural and peritoneal effusion; 6) Unable to obtain clear ultrasound images or other factors unsuitable for inclusion in the study; 7) Current participation in another interventional clinical trial. 2 Control group: 1) Patients with chest, lung, mediastinal, or respiratory center related diseases; 2) The subjects are unable to cooperate in completing the study, unable to obtain clear ultrasound images, or other factors that are not suitable for inclusion in the study; 3) Current participation in another interventional clinical trial.

Design outcomes

Primary

MeasureTime frame
Diaphragm excursion;Alternative position of diaphragm excursion;

Secondary

MeasureTime frame
Splenic excursion;Pleural sliding displacement;Liver excursion;Renal excursion;

Countries

China

Contacts

Public ContactZhao Haotian

Hebei General Hospital

1011192637@qq.com+86 151 0018 5988

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026