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An Empirical Study on Exercise Tolerance Characteristics and Exercise Rehabilitation in Patients with Stable Coronary Heart Disease

An Empirical Study on Exercise Tolerance Characteristics and Exercise Rehabilitation in Patients with Stable Coronary Heart Disease

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092834
Enrollment
Unknown
Registered
2024-11-25
Start date
2024-11-25
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

Stable Coronary Artery Disease

Interventions

Trial Group:Phase II Cardiac Rehabilitation with Pilates Ring
Control Group:Phase II Cardiac Rehabilitation

Sponsors

Beijing Sport University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. age >=18 years old and <=70 years old, male or female;2. complete imaging examination to confirm the diagnosis of CAD in the past year, and in a stable course of the disease; 3. did not participate in professional rehabilitation or exercise training in the past six months; 4. complete biochemical tests in the past three months; 5. can participate in and complete various tests; 6. voluntarily participate in the study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Current symptoms involved in other lifestyle intervention programs (such as nutrition, psychology, exercise, health education and other intervention programs); 2. Acute coronary symptoms or other congenital heart disease, valvular disease, severe neurosis caused by chest pain or heart function grade III or IV; 3. Patients with motor contraindications; 4. Patients with severe cardiopulmonary dysfunction; 5. Patients with severe primary diseases such as heart, brain, liver, kidney, hematopoietic system; 6. Hypertension patients with poor blood pressure control (> 160/90 mmHg), poor blood glucose control, severe arrhythmia, complete left bundle branch block; 7. Women who have or are ready to become pregnant or lactating; 8. 2014 physical activity preparation questionnaire + answers to questions 2, 3 and 6 to choose "yes"; 9. Quadriceps femoris lateral head muscle abdominal position skinfold thickness > 35 mm; 10. Unable to perform cardiopulmonary exercise test due to limb function or other physical dysfunction.

Design outcomes

Primary

MeasureTime frame
Left ventricular ejection fraction;Early Filling Velocity/Early Diastolic Tissue Velocity;Peak oxygen uptake;body mass index;body fat mass;coronary stenosis;coronary stenosis %;Maximal isometric strength;grip strength;Root Mean Square;Muscle oxygen saturation;Muscle oxygen saturation at peak;

Secondary

MeasureTime frame
skeletal muscle mass;Visceral fat mass;Thin limb mass;High density lipoprotein;Low density lipoprotein;Fasting blood glucose;Peak Metabolicequivalents;peak oxygen pulse;respiratory quotient;

Countries

China

Contacts

Public ContactPeng Yuan

Beijing Sport University

vicky_bsu@163.com+86 177 0206 1992

Outcome results

None listed

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