Ancient chinese exercise tested to protect lungs from COPD
NCT ID NCT05940480
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This pilot study tests whether TCM Daoyin, a traditional Chinese movement and breathing therapy, can improve lung function and exercise ability in 60 adults aged 40-75 who are at risk for early chronic obstructive pulmonary disease (COPD). Participants will be randomly assigned to receive Daoyin training or standard care, and researchers will measure changes in lung function, walking distance, and immune markers. The goal is to see if this gentle practice can help slow or prevent lung decline.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2023
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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40 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Subject at-risk for COPD (Chronic obstructive pulmonary disease screening questionnaire (COPD-SQ) score≥16; and pre-bronchodilator FEV1/FVC ≥ 0.70, or pre-bronchodilator FEV1/FVC\<0.70 but post-bronchodilator FEV1/FVC ≥ 0.70). * Aged 40 to 75, male or female. * Subject has a clear mind and the ability to lead an independent life. * Subject agrees to perform a blood-test. * Subject agrees to participate in this study and sign to the informed consent. Exclusion Criteria: * Subject with acute exacerbation of COPD. * Subject with respiratory infectious disease (e.g., tuberculosis, influenza, etc.) within 1 month. * Subject with serious current unstable physical illness and mental illness. * Subject with definite clinical diagnosis of Alzheimer's disease, or severe cognitive impairment. * Subject is pregnant or lactating women.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Changzheng Community Health Service Center of Putuo District, Shanghai
Shanghai, Shanghai Municipality, 200333, China
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Shanghai Qigong Research Institute
Shanghai, Shanghai Municipality, 021, China
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