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Effect of pulmonary rehabilitation prescription combined with acupuncture on the rehabilitation of patients with stable chronic obstructive pulmonary disease

Effect of pulmonary rehabilitation prescription combined with acupuncture on the rehabilitation of patients with stable chronic obstructive pulmonary disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076255
Enrollment
Unknown
Registered
2023-09-28
Start date
2023-10-01
Completion date
Unknown
Last updated
2023-10-03

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:Conventional Western medicine treatment
Exercise group:Conventional Western medicine treatment+Exercise
Acupuncture group:Conventional Western medicine treatment+Acupuncture
Exercise combined with acupuncture group:Conventional Western medicine treatment+Exercise+Acupuncture

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. Participants meet the diagnostic criteria for COPD; 2. Participants are in GOLD 1-3 for severity; 3. Participants are stable (no acute exacerbation admissions and associated medication changes) for 4 weeks prior to randomization; 4. 40 years old = age = 80 years old, gender is not limited; 5. Participants understand, agree to participate in the study and signed an informed consent form.

Exclusion criteria

Exclusion criteria: 1. COPD combined with other respiratory diseases such as lung cancer, asthma, etc.; COPD combined with other cardiovascular, endocrine, liver and other major diseases, which are unable to perform acupuncture and exercise; 2. Cardiac disease that prevents exercise endurance and other tests; with musculoskeletal disease or open injury, not suitable for limb muscle strength assessment; 3. Severe speech, attention, auditory, visual, intellectual, psychiatric, or cognitive impairments that prevent them from cooperating with treatment and assessment; 4. Concurrent participation in other clinical intervention-type or drug-type trials; 5. Women of childbearing age who are pregnant or breastfeeding, have plans to have a child within six months, have a positive pregnancy test, and are unable to use effective contraception for the duration of the trial 6. Those who are not suitable for acupuncture treatment, such as fear of acupuncture or the phenomenon of needle fainting, and those who have broken skin, infection or ulcers at the site of acupuncture point selection; 7. Participating in various forms of regular exercise (>2 times per week, 60min/time) for 6 months prior to the trial; 8. Participants received acupuncture treatment 1 month prior to the trial; 9. Those who are considered by the investigator to be unsuitable for participation in the clinical trial.

Design outcomes

Primary

MeasureTime frame
six minutes walk test;

Secondary

MeasureTime frame
pulmonary function;diaphragm function;airway structure;airway impedance ;cardiopulmonary exercise capacity;Skeletal muscle strength;Surface electromyography;myoarchitecture;modified Medical Research Council;St George's respiratory questionnaire;COPD assessment test;Physical Activity Scale for the Elderly;International Physical Activity Questionnaire;psychological assessment;TCM Syndrome Points;

Countries

China

Contacts

Public ContactWei Zhang

Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine

zhangw1190@sina.com+86 130 2315 3956

Outcome results

None listed

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