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Energy metabolism characteristics of Baduanjin exercise on healthy human and patients with stable coronary artery disease

Study on the establishment and clinical assessment of integrated treatment of traditional Chinese and western medicine for stable coronary artery disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ROC-17014146
Enrollment
Unknown
Registered
2017-12-25
Start date
2017-12-25
Completion date
Unknown
Last updated
2018-01-08

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

Conditions

stable coronary artery disease

Interventions

healthy human group:Practicing the first phase of Buanduanjin exercise, including resting state before exercise in 3min, the preparatory, from the first to the eighth form and closed form in 12min, an
stable coronary artery disease group:Practicing from the first to the second phase of Buanduanjin exercise, including resting state before exercise in 3min, repeating the preparatory, from the first t

Sponsors

First Teaching Hospital of Tianjin University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 79 Years

Inclusion criteria

Inclusion criteria: 1. Healthy human: (1) Aged 35 to 79 years; (2) BMI 19 to 24[BMI=weight(kg)/height2(m2)]; (3) Without heart, liver, lung, kidney and other important organ diseases,without digestive system, respiratory system, circulatory system, blood system, endocrine system, nervous system and mental disorders; (4) No positive signs of clinical significance by physical examination; (5) Submitted informed consent. 2. Patients with stable coronary heart disease: (1) Aged 35 to 79 years; (2) Compliance with diagnostic criteria of stable coronary heart disease; (3) Classification of CCS cardiac function beween I-III; (4) Submitted informed consent.

Exclusion criteria

Exclusion criteria: 1. Healthy human: (1) Unable to exercise due to limb disorders or other reasons; (2) Women in pregnancy or lactation; (3) Other situations that researchers considered not suitable for the trial. 2. Patients with stable coronary heart disease: (1) Left main coronary artery stenosis; (2) Uncontrolled hypertension or systolic pressure=160mmHg and/or diastolic pressure=100mmHg after taken medicine; (3) Uncontrolled rapid arrhythmias with symptoms or hemodynamic disorders; (4) High or complete atrioventricular block; (5) acute endocarditis; (6) Obstructive hypertrophic cardiomyopathy; (7) Symptomatic severe aortic stenosis, decompensated heart failure, acute pulmonary embolism, deep vein thrombosis, acute pericarditis, myocarditis and acute aortic dissection; (8) Chronic pulmonary disease with dyspnea; (9) Stroke or transient ischemic attack with cognitive impairment in the short term; (10) The clinical problems that have not been corrected, such as infection, severe anemia, electrolyte disorder, hyperthyroidism, etc; (11) The abnormal function of liver and kidney (serum alanine aminotransferase or creatinine > 2 times the upper limit of normal reference value); (12) Unable to exercise due to limb disorders or other reasons; (13) Women in pregnancy or lactation; (14) Other situations that researchers considered not suitable for the trial.

Design outcomes

Primary

MeasureTime frame
metabolic equivalent;

Secondary

MeasureTime frame
oxygen uptake (VO2);VO2/kg;VO2/HR;carbon dioxide output(VCO2);minute ventilation(VE);VCO2/VO2;tidal volume(VT);respiration frequency(Rf);VE/VCO2;VE/VO2;the end-tidal CO2 pressures(PetCO2);st-segment deviation;heart rate recovery in 1min (HRR1);Borg Scale;

Countries

China

Contacts

Public ContactWang Xianliang

First Teaching Hospital of Tianjin University of Traditional Chinese Medicine

xlwang1981@126.com+86 13920007825

Outcome results

None listed

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