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Application of intelligent pulmonary rehabilitation system in patients with stable chronic obstructive pulmonary disease

Application of intelligent pulmonary rehabilitation system in patients with stable chronic obstructive pulmonary disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101076
Enrollment
Unknown
Registered
2025-04-18
Start date
2025-04-27
Completion date
Unknown
Last updated
2025-04-21

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

Conditions

COPD

Interventions

Routine exercise training group:Pulmonary-based Qigong exercise. The intervention time was 3 days/week, 1 time/day, 60min/ time for 8 weeks
AI respiratory rehabilitation team:AI respiratory rehabilitation. The intervention time was 3 days/week, 1 time/day, 60min/ time for 8 weeks

Sponsors

Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic criteria for COPD; (2) The severity is in the GOLD 1-3 level; (3) Stable 4 weeks before randomization (no acute exacerbations and related drug changes); (4) Age <= 40 years old <= 80 years old, gender is not limited; (5) Understand and agree to participate in this study and sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) COPD combined with lung cancer, asthma and other respiratory diseases, COPD combined with other cardiovascular, endocrine, liver and other major diseases, unable to perform acupuncture and exercise; (2) suffering from heart disease and unable to perform exercise endurance tests; Those with musculoskeletal disease or open injury are not suitable for limb muscle strength assessment; (3) severe speech, attention, hearing, vision, intellectual, mental, or cognitive impairment that cannot be treated and evaluated; (4) Participating in other clinical intervention or drug trials; (5) Women of childbearing age are pregnant or lactating, have a birth plan within six months, have a positive pregnancy test, and cannot take effective contraceptive measures during the test; (6) Participate in various forms of regular exercise (60min/ time > 2 times per week) for 6 months before the test; (7) Participants considered unsuitable for clinical trials.

Design outcomes

Primary

MeasureTime frame
6min walking test;30s sit-to-stand test;

Secondary

MeasureTime frame
Lung pulmonary;Diaphragm ultrasound;Respiratory muscle strength;30s elbow flexion test;Modified Medical Research Council Dyspnea Scale;St. George's Respiratory Questionnaire;COPD Assessment Test;Hamilton Anxiety Scale;Hamilton Depression Scale;

Countries

China

Contacts

Public ContactHe Yuchen

Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine

519122134@qq.com+86 137 6111 2395

Outcome results

None listed

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