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Clinical Trials/NCT06681506
NCT06681506
Recruiting
N/A

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

Shanghai 10th People's Hospital1 site in 1 country100 target enrollmentJanuary 1, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
Ischemic Heart Disease
Sponsor
Shanghai 10th People's Hospital
Enrollment
100
Locations
1
Primary Endpoint
Change from baseline myocardial infarct area at 6 months
Status
Recruiting
Last Updated
last year

Overview

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

Registry
clinicaltrials.gov
Start Date
January 1, 2024
End Date
December 31, 2031
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Shanghai 10th People's Hospital
Responsible Party
Principal Investigator
Principal Investigator

Ya-Wei Xu

Chief Physician

Shanghai 10th People's Hospital

Eligibility Criteria

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

Outcomes

Primary Outcomes

Change from baseline myocardial infarct area at 6 months

Time Frame: 1 day of inclusions and 6 months after the first treatment.

The location and extent of myocardial infarction were determined by D-SPECT.

Secondary Outcomes

  • 6 months hemodynamic changes in relative to the baseline(1 day of inclusions and 6 months after the first treatment.)
  • Change from baseline peak oxygen consumption at 6 months(1 day of inclusions and 6 months after the first treatment.)

Study Sites (1)

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