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A randomized controlled trial of phase I cardiac rehabilitation program based on the IKAP model for heart failure patients

A randomized controlled trial of phase I cardiac rehabilitation program based on the IKAP model for heart failure patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097663
Enrollment
Unknown
Registered
2025-02-24
Start date
2025-03-01
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

cardiac failure

Interventions

Intervention group:Experimental group: On the basis of the control group, I-stage cardiac rehabilitation with IKAP mode was implemented. I(information collection): collect basic information on the fir
K(Knowledge transfer): knowledge transfer on five prescriptions of cardiac rehabilitation
A(Attitude changes ideas): 3 days after admission-before the condition is stable and the exercise prescription can be implemented, strengthen the propaganda content
P(Practice urges action): Exercise prescription can be implemented when the condition is stable: 7-step exercise for phase I cardiac rehabilitation.
control group:Give patients routine treatment and care, including medication, diet guidance, intake control, health education, rehabilitation activities guidance, etc.

Sponsors

Sun Yat-sen Memorial Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic criteria for chronic heart failure as outlined in the "2024 Chinese Heart Failure Diagnosis and Treatment Guidelines" confirmed by a cardiologist; (2) Patients with stable heart failure with New York Heart Association (NYHA) functional class II-III; (3) Acute decompensated heart failure (including acute exacerbation of chronic heart failure), with stable vital signs and no contraindications to activity; (4) Conscious, with normal communication and reading ability, and no limb movement disorders; (5) Willing to participate and sign the informed consent form;

Exclusion criteria

Exclusion criteria: (1) Early acute coronary syndrome (within 2 days); (2) Malignant arrhythmia; (3) Acute heart failure (hemodynamically unstable); (4) Resting blood pressure >200/110 mmHg; (5) High-degree atrioventricular block; (6) Acute myocarditis, pericarditis, or endocarditis; (7) Symptomatic severeortic stenosis; (8) Severe hypertrophic obstructive cardiomyopathy; (9) Acute systemic disease; (10) Intracard thrombus; (11) Progressive worsening of resting dyspnea or reduced exercise tolerance in the last 3-5 days; (12) Se myocardial ischemia with low power exercise load (1.8 kg in the past 1-3 days; (18) Currently receiving intermittent or continuous dopamine treatment; (19) Systolic blood pressure drops during exercise; (20) NYHA Class IV heart function; (21) Complex ventricular arrhythmias rest or exertion; (22) Resting heart rate >=100 beats/min in the supine position; (23) Diseases that limit; (24) Severe liver and kidney dysfunction; (25) Severe lung disease (e.g., acute exacerbation of COPD, severe infection, etc. (26) In the terminal stage of other serious diseases (e.g., advanced malignant tumors).

Design outcomes

Primary

MeasureTime frame
6-minute walking distance;

Secondary

MeasureTime frame
Brain natriuretic peptide (BNP);Minnesota Living with Heart Failure Questionnaire, MLHFQ;Self-Care Maintenance and Management Inventory;Generalized Anxiety Disorder-7;Patient Health Questionnaire-9;readmission rate;length of stay;

Countries

China

Contacts

Public ContactLai Jianqing

Sun Yat-sen Memorial Hospital of Sun Yat-sen University

787028726@qq.com+86 159 8910 7614

Outcome results

None listed

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