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Research on the application of time-effective stimulation in pulmonary rehabilitation after intubation in AECOPD patients

Research on the application of time-effective stimulation in pulmonary rehabilitation after intubation in AECOPD patients

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116701
Enrollment
Unknown
Registered
2026-01-14
Start date
2026-01-20
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

Acute exacerbation of chronic obstructive pulmonary disease

Interventions

Trial group:Based on conventional pulmonary rehabilitation, add a time-sensitive motivational nursing intervention program. Emotional motivation: Use communication, psychological support, family vis
Control group:Conventional pulmonary rehabilitation includes passive and active training. Passive training: Passive joint range-of-motion exercises, positioning, inspiratory muscle training, airway

Sponsors

Northern Jiangsu People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients who meet the diagnostic criteria for AECOPD as per the "Guidelines for the Diagnosis and Treatment of Chronic Obstructive Pulmonary Disease", have undergone endotracheal intubation treatment, passed the SBT test, and meet the conditions for weaning and extubation; 2.Patients aged 18 years or older, with clear consciousness, normal comprehension ability, limb muscle strength of grade 3 or above, and the ability to independently or cooperatively perform pulmonary rehabilitation training; 3.Both the patients themselves and/or their families have been informed of the research content and voluntarily participate.

Exclusion criteria

Exclusion criteria: 1.Presence of other respiratory diseases; 2.History of pulmonary embolism, tuberculosis, hemoptysis, or pneumothorax; 3.Physical disability; 4.Comatose state; 5.Mental illness/disorder;

Design outcomes

Primary

MeasureTime frame
Compliance rate of pulmonary rehabilitation training in AECOPD patients after extubation;

Secondary

MeasureTime frame
Cough and Sputum Production Capacity;Pulmonary function assessment;The re-intubation rate within 48 hours after extubation in patients with AECOPD;Arterial Blood Gas Analysis;Degree of dyspnea;

Countries

China

Contacts

Public ContactZhang Biyuan

Northern Jiangsu People's Hospital

865842982@qq.com+86 514 87373183

Outcome results

None listed

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