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Application of acupoint external counterpulsation in cardiac rehabilitation

Application of acupoint external counterpulsation in cardiac rehabilitation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000918
Enrollment
Unknown
Registered
2025-05-07
Start date
2024-07-23
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Coronary heart disease

Interventions

Healthy person group:The patients were randomly divided into experimental group and control group by two-stage crossover design, and the treatment was once. After a 2-week elution period, crossover w
group of acupoint external counterpulsation:Acupoint external counterpulsation
group of conventional external counterpulsation:Conventional external counterpulsation

Sponsors

Dongzhimen Hospital Beijing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 85 Years

Inclusion criteria

Inclusion criteria: Healthy individuals: aged between 25 and 35 years old with a BMI of =18 and =25 kg/m2 regardless of gender. The subjects gave informed consent and voluntarily signed the informed consent form. Patient :(1) Gender is not limited and meets the diagnostic criteria for coronary heart disease; (2) More than one month after complete revascularization; (3) Mild to moderate patients with a GAD-7 or (and)PHQ-9 score of 5 to 14 points; (4) Age: 30 to 85 years old; (5) The subjects gave informed consent and voluntarily signed the informed consent form.

Exclusion criteria

Exclusion criteria: Healthy individuals :(1) Have any cardiovascular endocrine kidney or liver hematological immune system or infectious diseases; (2) Has received drug treatment within the past month; (3) Smokers and drinkers; (4) Exercise training was conducted one week before the start of the study; (5) There are contraindications for external counterpulsation. Patients :(1) Those with severe valvular heart disease obstructive cardiomyopathy or other non-ischemic heart diseases and grade IV cardiac function; (2) Those with a history of severe primary diseases of the liver kidneys nervous system and hematopoietic system as well as severe mental disorders; (3) Those at the stage of pregnancy or conception; (4) Patients who have used any anti-anxiety and/or antidepressant drugs within the past 3 months; (5) There are contraindications for external counterpulsation

Design outcomes

Primary

MeasureTime frame
Hamilton Anxiety Scale (HAMA) scores and Hamilton Depression Scale (HAMD) scores were recorded;

Secondary

MeasureTime frame
Parameters related to heart rate variability;Seattle Angina Questionnaire,SAQ;Cardiopulmonary exercise test related indicators;The changes of serum monoamine neurotransmitters were detected;Autonomic nerve function score;Non-invasive hemodynamic parameters;Targeted exosome protein antibody chip;Myokines related indicators;Pittsburghsleepqualityindex,PSQI;Non-targeted metabolomics;Related indicators of cognitive function;

Countries

China

Contacts

Public ContactHan Xiaowan

Dongzhimen Hospital Beijing University of Chinese Medicine

965396781@qq.com18810263577

Outcome results

None listed

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