Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT03180320

Baduanjin-eight-silken-movement With Self-efficacy Building for Patients With Chronic Heart Failure (BESMILE-HF Study)

Led by Guangdong Provincial Hospital of Traditional Chinese Medicine · Updated on 2025-05-18

150

Participants Needed

1

Research Sites

401 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Chronic heart failure (CHF) is a major and growing public health problem and poses economic burden on the society. There is a need for a safe, equipment-free, low-cost, and easily implemented exercise-based cardiac rehabilitation program for CHF patients in China. Baduanjin exercise, translated as 'eight silken movements', is one of the most common forms of traditional Chinese exercise and it could have value to be integrated into a exercise-based cardiac rehabilitation program for CHF patients, together with education, evaluation and consultancy. Accordingly, the BESMILE-HF program applying the Baduanjin exercise as the central component, has been developed in Guangdong Provincial Hospital of Chinese Medicine which is one of the largest hospitals of Chinese medicine in China. This project is to evaluate the efficacy and acceptability of BESMILE-HF program in patients with CHF in China, and it will be based on a randomized controlled trial and a qualitative study.

CONDITIONS

Official Title

Baduanjin-eight-silken-movement With Self-efficacy Building for Patients With Chronic Heart Failure (BESMILE-HF Study)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Diagnosed with chronic heart failure
  • Symptoms and signs stable for at least 1 month
  • NYHA functional class II or III
Not Eligible

You will not qualify if you...

  • Contraindications to cardiopulmonary test
  • Contraindications to exercise training
  • Serious acute or chronic organic disease or mental disorders
  • Cardiac surgery, resynchronization therapy, or intracardiac defibrillation within past 3 months
  • Cardiac arrest within past 1 year
  • History of peripartum cardiomyopathy, hyperthyroid heart disease, or primary pulmonary hypertension
  • Unable to perform a bicycle stress test
  • Severe cognitive dysfunction preventing informed consent or understanding
  • Current regular Baduanjin exercise or participation in a cardiac rehabilitation program
  • Currently participating in another clinical trial

AI-Screening

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Trial Site Locations

Total: 1 location

1

Guangdong Provincial Hospital of Chinese Medicine

Guangzhou, Guangdong, China, 510120

Actively Recruiting

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Research Team

W

Weihui Lu

CONTACT

X

Xiankun Chen

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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