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Clinical study on the influence of Baduanjin on health outcome and behavior habits of patients with stable COPD

Clinical study on the influence of Baduanjin on health outcome and behavior habits of patients with stable COPD

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100049418
Enrollment
Unknown
Registered
2021-08-02
Start date
2021-07-23
Completion date
Unknown
Last updated
2022-04-19

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

Experimental group:Baduanjin + conventional treatment
control group:conventional treatment

Sponsors

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. In line with the diagnostic criteria of the 2017 GOLD guidelines, COPD is divided into groups A, B, and C (group A: low risk, few symptoms, group B: low risk, multiple symptoms, group C: high risk, few symptoms) ; 2. In the stable stage of COPD (the stable stage refers to the patients whose symptoms such as cough, expectoration and shortness of breath are stable or mild, and the condition basically returns to the state before the acute exacerbation); 3. Aged 40 to 85 years; 4. Able to complete various assessments required by the research; 5. Those who participated voluntarily and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Suffering from concomitant diseases that can interfere with evaluation, treatment and follow-up (epilepsy, unstable cardiovascular disease, active malignant tumor, severe lower extremity disease, severe neurological impairment, etc.); 2. Have undergone standard pulmonary rehabilitation exercise training or Baduanjin training before joining the group; 3. Those who cannot walk or have severe cognitive impairment; 4. Patients with high risk of falls and balance dysfunction.

Design outcomes

Primary

MeasureTime frame
maximal oxygen uptake;Moderate to high-intensity physical activity;anaerobic threshold;

Secondary

MeasureTime frame
breathlessness measurement using the modified British Medical Research Council;chronic obstructive pulmonary disease assessment test;Activities of daily living;Pulmonary function;Health Status Survey Short Form;resting oxygen uptake;

Countries

China

Contacts

Public ContactCai Qian

Guangdong Provincial Hospital of Chinese Medicine

13560114917@163.com+86 13560114917

Outcome results

None listed

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