Skip to content

A New Cardiac Rehabilitation Treatment in the Application of Ischemic Heart Disease

A New Cardiac Rehabilitation Treatment in the Application of Ischemic Heart Disease: a Prospective, Randomized Controlled Clinical Study

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06681506
Enrollment
100
Registered
2024-11-08
Start date
2024-01-01
Completion date
2031-12-31
Last updated
2024-11-08

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

Conditions

Cardiac Rehabilitation, Ischemic Heart Disease

Keywords

coronary atherosclerotic cardiopathy, Cardiac Shock Wave Therapy, exercise rehabilitation, cardiac rehabilitation, Ischemic Heart Disease

Brief summary

Cardiac rehabilitation is an important link in cardiovascular disease. This study mainly explores the effectiveness of new cardiac rehabilitation therapy (early respiratory rehabilitation, phase I rehabilitation, exercise therapy, external counterpulsation, extracorporeal shock wave, etc.) on patients with ischemic heart disease such as coronary heart disease and heart failure, and the compliance of home rehabilitation compared with traditional cardiac rehabilitation therapy (traditional exercise rehabilitation, rehabilitation education, etc.).

Detailed description

This study is a prospective, randomized, controlled study, follow the principle of PICOST design, specific as follows: Participants (the list) : preliminary clinical diagnosis of coronary atherosclerotic heart disease, heart failure. Intervention (Intervention) : conventional drug therapy + new cardiac rehabilitation therapy, a new cardiac rehabilitation treatment reference guide requirements, according to the actual circumstance of patients treated with 1-3 months Intervention. Comparator(control): conventional drug therapy + traditional cardiac rehabilitation therapy. The traditional cardiac rehabilitation therapy referred to domestic and international guidelines and consensus, and used 1 week-3 months of treatment intervention according to the actual situation of patients. Outcome (the end) : the primary end point: D\_SPECT examination, were followed up for 6 months to evaluate myocardial perfusion imaging is reduce ischemic area. The secondary end point: 1) the blood biochemical examination and myocardial necrosis markers, etc.; 2) the cardiopulmonary exercise testing: maximum kilograms oxygen uptake and anaerobic threshold when the maximum kilograms oxygen uptake; 3) the major adverse cardiovascular events: cardioascular death, non-fatal myocardial infarction, unplanned coronary artery reconstruction, stroke, heart failure and angina associated hospitalized again; 4) patients family rehabilitation treatment adherence

Interventions

DEVICEMetronomic breathing, exercise rehabilitation, external counterpulsation, extracorporeal shock wave.

Phase I rehabilitation(Metronomic breathing,exercise rehabilitation),Phase II rehabilitation (exercise rehabilitation, external counterpulsation, extracorporeal shock) wave.)

DEVICEbedside rehabilitation and breathing, balance, flexibility, movement rehabilitation

Phase I rehabilitation (bedside rehabilitation, breathing rehabilitation), Phase II rehabilitation (breathing, balance, flexibility, movement)

Sponsors

Shanghai Municipal Science and Technology Commission
CollaboratorOTHER_GOV
Shanghai 10th People's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Aged between 18 and 85 years old * Female subjects no pregnancy * The main admission diagnosis of ischemic heart disease (coronary heart disease, myocardial infarction, ischemic heart failure, etc.) * The need for cardiac rehabilitation treatment

Exclusion criteria

* acute respiratory distress syndrome (ARDS); * acute episode of COPD; * uncontrolled pulmonary infection; * acute heart failure; acute pulmonary embolism; * acute myocarditis/pericarditis; * severe arrhythmia (degree II or III atrioventricular block, atrial flutter, or atrial fibrillation); * sternotomy, rib fracture, thoracic deformity, or other neurological diseases that may affect respiratory muscles

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline myocardial infarct area at 6 months1 day of inclusions and 6 months after the first treatment.The location and extent of myocardial infarction were determined by D-SPECT.

Secondary

MeasureTime frameDescription
6 months hemodynamic changes in relative to the baseline1 day of inclusions and 6 months after the first treatment.Noninvasive hemodynamic evaluation of hemodynamic state, such as, the larger the value of Stroke volume, Stroke volume index, Cardiac output, Cardiac output index parameters, the smaller the value of Systemic vascular resistance, Systemic vascular resistance index parameters, the better the function of the patient's heart and arterial vessels.
Change from baseline peak oxygen consumption at 6 months1 day of inclusions and 6 months after the first treatment.maximum oxygen and maximum kilogram oxygen uptake accessed during Cardiopulmonary Exercise Testing (CPET)

Other

MeasureTime frameDescription
Major adverse cardiovascular events (MACE)From the date of inclusion until the date of documented adverse events with 6 monthscardiovascular death, non-fatal myocardial infarction, unplanned coronary revascularization, stroke, heart failure, and angina-related rehospitalization
Other treatment-related adverse reactionsFrom the date of inclusion until the date of treatment-related adverse reactions within 6 months

Countries

China

Contacts

Primary Contactliujing liu, MD, PhD
liuweijing98@sina.com+86 18917684041
Backup Contactzhaoxin zhu, B.D
zhaoxinzhu0728@163.com+86 13162999337

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026