Asaf Harofe Medical Center
Beer Yaacov, Israel
NCT Number: NCT02162290
The research will study the differences between interval training and continuous training among cardiac patients in a cardiac rehabilitation facility.
The main objectives are:
1. Functional capacity measures (VO2 max). 2. Cardiac risk factors 3. Quality of life assessments.
Study hypothesis:
Interval training will be more effective in improving functional capacity, cardiac risk factors and quality of life, compared to continuous training.
Looking for future studies?
Notify Me40 year–75 year
All sexes
Interventional
Not applicable
Beer Yaacov, Israel
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Exercise bouts in low and high intensities
Time frame: 9 months
Outcome is assessed at baseline, after 3 months and at nine months
Assaf-Harofeh Medical Center
Other Gov
Comparison Between Moderate-high Interval Exercise and Moderate Continuous Exercise in an Advanced Cardiac Rehabilitation Program - Nine Months Follow up
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT03419325
Acute Coronary Syndrome, Arterial Occlusive Diseases
Carolina, Puerto Rico
View Trial DetailsNCT05336435
Acute Coronary Syndrome, Angina Pectoris
Aabenraa, Denmark
View Trial DetailsNCT07519590
Arterial Occlusive Diseases, Arteriosclerosis
Cairo, Cairo Governorate, Egypt
View Trial DetailsNCT05966662
Arterial Occlusive Diseases, Arteriosclerosis
Huntsville, Alabama, United States
View Trial Details