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Effect of a 5G Smart Terminal-based Respiratory Muscle Load Training Combined with Diaphragmatic Sputum Drainage on Respiratory Function in Hospitalized COPD Patients: A Latent Class Growth Study

Effect of a 5G Smart Terminal-based Respiratory Muscle Load Training Combined with Diaphragmatic Sputum Drainage on Respiratory Function in Hospitalized COPD Patients: A Latent Class Growth Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123959
Enrollment
Unknown
Registered
2026-05-05
Start date
2026-05-06
Completion date
Unknown
Last updated
2026-05-11

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

Conditions

Chronic Obstructive Pulmonary Disease

Interventions

intervention group:All patients used the 5G intelligent respiratory rehabilitation terminal and received daily 1-2 sessions of respiratory muscle threshold load training combined with external diaphra

Sponsors

Guizhou University of Traditional Chinese Medicine/The Second Affiliated Hospital of Guizhou University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. COPD inpatients meeting the GOLD 2025 diagnostic criteria, with mMRC dyspnea score >= 2 at admission; 2. Age between 60 and 85 years old; 3. Expected hospital stay of 7 to 15 days; 4. Able to cooperate with daily rehabilitation training; 5. Possess basic equipment operation skills (for 5G smart terminal interaction); 6. Voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients requiring invasive or non-invasive mechanical ventilation; 2. Presence of pneumothorax, active hemoptysis, unstable angina, or acute myocardial infarction; 3. Coexisting severe neurological diseases (e.g., post-stroke dysphagia), musculoskeletal disorders, or malignant tumors that interfere with rehabilitation; 4. Cognitive impairment or psychiatric disorders preventing cooperation with training; 5. Participation in other respiratory rehabilitation clinical trials within one month prior to admission; 6. Inability to complete at least 7 days of inpatient rehabilitation.

Design outcomes

Primary

MeasureTime frame
Maximal Inspiratory Pressure (PImax);

Secondary

MeasureTime frame
24-hour sputum output;Maximum expiratory pressure;Percentage of FEV1 relative to the predicted value;

Countries

China

Contacts

Public ContactWang Mingzhen

Guizhou University of Traditional Chinese Medicine/The Second Affiliated Hospital of Guizhou University of Traditional Chinese Medicine

m_z_wang@foxmail.com+86 135 9500 8482

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 16, 2026