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Effects of Chuzhen technique on sleep quality in patients with chronic heart failure of deficiency of both qi and Yin

Effects of Chuzhen technique on sleep quality in patients with chronic heart failure of deficiency of both qi and Yin

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001338
Enrollment
Unknown
Registered
2026-05-26
Start date
2025-04-10
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Chronic heart failure

Interventions

Control Group:routine treatment care
Experimental Group:Implement cudgel acupuncture intervention based on the control group.

Sponsors

Chengdu University of Traditional Chinese Medicine Affiliated Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Meets the diagnostic criteria for CHF; (2) Meets the diagnostic criteria for deficiency of both qi and yin in traditional Chinese medicine; (3) Age between 45 and 75 years old; (4) Cardiac function classified as Grade II-III; (5) PSQI > 7 points; (6) Voluntarily participates in this study and signs the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients with severe primary cardiogenic diseases such as cardiogenic shock, second-degree or higher atrioventricular block, and life-threatening arrhythmias; (2) Patients with primary diseases involving abnormal liver or kidney function, or dysfunction of the digestive, endocrine, or hematopoietic systems; (3) Patients with severe bleeding tendencies or platelet count (PLT) < 50×10^9/L; (4) Diseases or symptoms associated with high mortality, such as acute myocardial infarction, cerebral hemorrhage, cardiac tamponade, severe constrictive pericarditis, or pulmonary embolism; (5) Patients undergoing other treatments that may affect the evaluation of sleep improvement (e.g., sedative-hypnotic drugs); (6) Women in pregnancy or lactation; (7) Patients with skin integrity compromised at the treatment site, such as eczema, scabies, or ulceration; (8) Patients with severe psychological disorders, mental illnesses, or cognitive impairments; (9) Patients currently participating in other clinical trials. (Note: Participants meeting any one of the above criteria will be excluded.)

Design outcomes

Primary

MeasureTime frame
Pittsburgh Sleep Quality Index (PSQI) Score;

Secondary

MeasureTime frame
Insomnia Severity Index (ISI) Score;Hospital Anxiety and Depression Scale (HADS) Score;Minnesota Living with Heart Failure Questionnaire (MLHFQ) score;N-terminal pro-B-type natriuretic peptide level;

Countries

China

Contacts

Public ContactFeng Juan

Hospital of Chengdu University of Traditional Chinese Medicine

2861205674@qq.com15882001398

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Jun 11, 2026