Coronary Artery Disease Clinical Trial
Official title:
Influence of Interval Aerobic Exercise Training on Cardiorespiratory and Metabolic Variables and Inflammatory Markers in Patients With Different Level of Coronary Artery Lesions
The purpose of this study is to investigate the effects of interval training, based-intensity on 70% at 110% of oxygen consumption and workload attained on ventilatory anaerobic threshold, on aerobic functional capacity, autonomic modulation of heart rate, metabolic profile in patients with and without coronary artery disease.
Background: Exercise training has been essential component of the cardiac rehabilitation.
However, it is not known if interval training based on ventilatory anaerobic threshold could
be effective for improving aerobic functional capacity and metabolic profile.
Objective:To investigate the effects of interval training, based-intensity on 70% at 110% of
oxygen consumption and workload attained on ventilatory anaerobic threshold, on aerobic
functional capacity, autonomic modulation of heart rate, metabolic profile in patients with
and without coronary artery disease.
Design: Prospective randomized controlled trial. Subjects: 68 men between 40 and 65 years
old.
All subjects will be submitted:
1. - Clinical assessment: personal data, lifestyle and food, family history, current and
previous history of disease.
2. - Physical examination: cardiac and lung auscultation,measurement of heart rate, blood
pressure, body weight and height.
3. - Heart rate will be recorded at rest, in the supine position for 15 min, standing
position for 10 min and respiratory sinus arrhythmia maneuver.
4. - Submaximal or symptom-limited cardiopulmonary exercise test on cycle ergometer will
be performed to determined the ventilatory anaerobic threshold.
5. - Two cardiopulmonary exercise testing on treadmill at constant workload (moderate and
high intensity). Expiratory flow limitation will be evaluated by flow-volume loops at
the end of each exercise workload.
6. - Blood samples will be collected to analyze glycemic and lipid profiles.
7. - After these procedures, the subjects will be randomly assigned to one of two groups,
trained group or control group.
8. - Interval training program will consist 30-40 minutes each exercise session, three
times a week for 16 weeks, with a workload determined on the basis of ventilatory
anaerobic threshold.
9. - At 48 hours after the last day of training, the subjects will repeat all experimental
procedures as in baseline testing. Controls will be retested 16 weeks after the
completion of baseline testing.
10. - All subjects will be instructed to maintain their habitual diet without a
standardized caloric restriction.
Thus, it is expected that interval training will promote beneficial physiological
adaptations in patients with and without coronary artery disease.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Investigator, Outcomes Assessor), Primary Purpose: Treatment
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
NCT06030596 -
SPECT Myocardial Blood Flow Quantification for Diagnosis of Ischemic Heart Disease Determined by Fraction Flow Reserve
|
||
| Completed |
NCT04080700 -
Korean Prospective Registry for Evaluating the Safety and Efficacy of Distal Radial Approach (KODRA)
|
||
| Recruiting |
NCT03810599 -
Patient-reported Outcomes in the Bergen Early Cardiac Rehabilitation Study
|
N/A | |
| Recruiting |
NCT06002932 -
Comparison of PROVISIONal 1-stent Strategy With DEB Versus Planned 2-stent Strategy in Coronary Bifurcation Lesions.
|
N/A | |
| Not yet recruiting |
NCT06032572 -
Evaluation of the Safety and Effectiveness of the VRS100 System in PCI (ESSENCE)
|
N/A | |
| Recruiting |
NCT04242134 -
Drug-coating Balloon Angioplasties for True Coronary Bifurcation Lesions
|
N/A | |
| Recruiting |
NCT05308719 -
Nasal Oxygen Therapy After Cardiac Surgery
|
N/A | |
| Completed |
NCT04556994 -
Phase 1 Cardiac Rehabilitation With and Without Lower Limb Paddling Effects in Post CABG Patients.
|
N/A | |
| Recruiting |
NCT05846893 -
Drug-Coated Balloon vs. Drug-Eluting Stent for Clinical Outcomes in Patients With Large Coronary Artery Disease
|
N/A | |
| Recruiting |
NCT06027788 -
CTSN Embolic Protection Trial
|
N/A | |
| Recruiting |
NCT05023629 -
STunning After Balloon Occlusion
|
N/A | |
| Completed |
NCT04941560 -
Assessing the Association Between Multi-dimension Facial Characteristics and Coronary Artery Diseases
|
||
| Completed |
NCT04006288 -
Switching From DAPT to Dual Pathway Inhibition With Low-dose Rivaroxaban in Adjunct to Aspirin in Patients With Coronary Artery Disease
|
Phase 4 | |
| Completed |
NCT01860274 -
Meshed Vein Graft Patency Trial - VEST
|
N/A | |
| Recruiting |
NCT06174090 -
The Effect of Video Education on Pain, Anxiety and Knowledge Levels of Coronary Bypass Graft Surgery Patients
|
N/A | |
| Terminated |
NCT03959072 -
Cardiac Cath Lab Staff Radiation Exposure
|
||
| Completed |
NCT03968809 -
Role of Cardioflux in Predicting Coronary Artery Disease (CAD) Outcomes
|
||
| Recruiting |
NCT05065073 -
Iso-Osmolar vs. Low-Osmolar Contrast Agents for Optical Coherence Tomography
|
Phase 4 | |
| Recruiting |
NCT04566497 -
Assessment of Adverse Outcome in Asymptomatic Patients With Prior Coronary Revascularization Who Have a Systematic Stress Testing Strategy Or a Non-testing Strategy During Long-term Follow-up.
|
N/A | |
| Completed |
NCT05096442 -
Compare the Safety and Efficacy of Genoss® DCB and SeQuent® Please NEO in Korean Patients With Coronary De Novo Lesions
|
N/A |