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Research on Integrated Rehabilitation for Chronic Obstructive Pulmonary Disease (COPD) Based on the Convergence of Medical and Rehabilitative Care

Research on Integrated Rehabilitation for Chronic Obstructive Pulmonary Disease (COPD) Based on the Convergence of Medical and Rehabilitative Care

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500109689
Enrollment
Unknown
Registered
2025-09-24
Start date
2025-10-31
Completion date
Unknown
Last updated
2025-09-29

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

Conditions

Chronic Obstructive Pulmonary Disease (COPD)

Interventions

Intelligent Rehabilitation group:1. Treatment decision system
2. Intelligent evaluation home care platform
3. Resource scheduling platform
Conventional Rehabilitation group:1. Manual assessment
2. Empirical treatment
3. Traditional consultation model

Sponsors

The First Affiliated Hospital of Xinxiang Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Meets the diagnostic criteria for severe COPD in the "Global Initiative for Chronic Obstructive Lung Disease (2025 edition)"; 2. Exercise function: Six-minute walk test 150-450 meters; 3. Ability to operate smart devices; 4. Aged 40-85 years, able to sign or authorize signing of the informed consent form; 5. Vital signs stable, medication controlling blood pressure < 180/100 mmHg.

Exclusion criteria

Exclusion criteria: 1. Merge with other patients with moderate to severe underlying diseases; 2. Severe cognitive impairment, MMSE < 10 points or unable to cooperate with assessment; 3. Implantation of electronic medical devices such as pacemakers, spinal cord stimulators, etc.; 4. Patients with acute infections; 5. Those who cannot perform standardized exercises due to combined neuromuscular system disorders or bone joint diseases, or are unsuitable for rehabilitation exercises due to combined issues like fractures or injuries; 6. Pregnant or breastfeeding women; 7. Individuals currently participating in other clinical trials for rehabilitation interventions; 8. Unable to use smart devices;9. Those deemed unsuitable for participation in this study based on comprehensive analysis by the researchers.

Design outcomes

Primary

MeasureTime frame
Efficiency of Rehabilitation Evaluation;Utilization Rate of Rehabilitation Resources;Rehabilitation expenditure as a percentage of total medical spending;Rehabilitation Intervention Rate;—

Secondary

MeasureTime frame
Total hospitalization costs (?);Satisfaction Assessment;Adverse Event Incidence Rate;Inpatient Stay Duration (days);—

Countries

China

Contacts

Public ContactHe Jiaojie

The First Affiliated Hospital of Xinxiang Medical University

843780412@qq.com+86 18236179501

Outcome results

None listed

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