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Research on the Application of Digital Therapeutics for Pulmonary Rehabilitation in Chronic Obstructive Pulmonary Disease-randomized controlled trial

Research on the Application of Digital Therapeutics for Pulmonary Rehabilitation in Chronic Obstructive Pulmonary Disease-randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124145
Enrollment
Unknown
Registered
2026-05-08
Start date
2026-05-13
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

Control group:Received intervention based on the traditional chronic obstructive pulmonary disease rehabilitation treatment model for 10 weeks
Experimental group:Received the intervention of the digital lung rehabilitation program for chronic obstructive pulmonary disease based on PDCA for 10 weeks

Sponsors

Beijing Chao-Yang Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Diagnosed with chronic obstructive pulmonary disease, with pulmonary function at GOLD 1-3 level; 2.Age ranging from 40 to 80 years old; 3.Possessing a smart phone and proficient in using apps; 4.Willing to undergo follow-up and having signed the informed consent form;

Exclusion criteria

Exclusion criteria: 1.Suffering from diseases such as tuberculosis-induced lung damage, thoracic deformity, extreme weakness, impaired vision or balance ability; 2.Suffering from malignant tumors, liver and kidney failure, bone and joint diseases, and other diseases causing limb movement disorders; 3.Having experienced unstable angina pectoris within the last month, acute myocardial infarction within half a year, severe arrhythmia, heart failure, and patients with hypertension whose blood pressure is not well controlled (systolic pressure > 140 mmHg and/or diastolic pressure > 90 mmHg); 4.Cognition impairment; 5.Combined respiratory failure; 6.Having participated in a pulmonary rehabilitation clinical trial within 6 months prior to enrollment; 7.Expected survival time of less than 1 year;

Design outcomes

Primary

MeasureTime frame
Change in CAT score before and after intervention;

Secondary

MeasureTime frame
The change of 6MWD, the improvement of lung function related indicators (FEV1, FEV1/FVC), and the improvement of average daily steps before and after intervention;Changes in mMRC grade, quality of life, anxiety and depression scale scores, and sleep quality (PSQI) before and after the intervention.;Adherence to pulmonary rehabilitation exercise, adherence to oral and/or inhaled medication, etc.;Types and proportions of adverse events;Incidence of acute exacerbations;

Countries

China

Contacts

Public ContactLiang Lirong

Beijing Chao-Yang Hospital, Capital Medical University

llrcruie@163.com+86 10 85231547

Outcome results

None listed

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