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Comparison Between Moderate-high Interval Exercise and Moderate Continuous Exercise in an Advanced Cardiac Rehabilitation Program

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ClinicalTrials.gov Identifier: NCT02162290
Recruitment Status : Completed
First Posted : June 12, 2014
Last Update Posted : May 17, 2016
Sponsor:
Information provided by (Responsible Party):
Assaf-Harofeh Medical Center

Study Description
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Brief Summary:

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.


Condition or disease Intervention/treatment Phase
Coronary Artery Disease Myocardial Infarction Other: Interval exercise training Other: Continuous exercise training Not Applicable

Study Design
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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 84 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Supportive Care
Official Title: Comparison Between Moderate-high Interval Exercise and Moderate Continuous Exercise in an Advanced Cardiac Rehabilitation Program - Nine Months Follow up
Study Start Date : May 2011
Actual Primary Completion Date : May 2015
Actual Study Completion Date : May 2015

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Arms and Interventions
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Arm Intervention/treatment
Experimental: Interval exercise
Exercise bouts in low and high intensities
 Other: Interval exercise training
Exercise bouts in low and high intensities
Experimental: Continuous exercise
Exercise continuously with moderate intensity
 Other: Continuous exercise training


Outcome Measures
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Primary Outcome Measures :
  1. Maximal functional capacity [ Time Frame: 9 months ]
    Outcome is assessed at baseline, after 3 months and at nine months


Eligibility Criteria
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Ages Eligible for Study:   40 Years to 75 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patients undergone:

    • Myocardial infarction
    • Percutaneous transluminal coronary angioplasty
    • Coronary artery bypass graft

Exclusion Criteria:

  • Patients with:

    • Severe ischemia or angina
    • Implantable cardioverter-defibrillator
    • Pacemakers transplants
    • Severe left ventricular dysfunctions
    • Uncontrolled arrhythmias
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02162290


Locations
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Israel
Asaf Harofe Medical Center
Beer Yaacov, Israel
Sponsors and Collaborators
Assaf-Harofeh Medical Center
Investigators
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Principal Investigator: Yael Pernick Asaf Harofe Medical Center
Study Director: Zyssman, MD Asaf Harofe Medical Center
Study Director: Jonathan Moore, PhD Bangor University
Study Director: Zvi Vered, MD Asaf Harofe Medical Center
More Information
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Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information
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Responsible Party: Assaf-Harofeh Medical Center
ClinicalTrials.gov Identifier: NCT02162290    
Other Study ID Numbers: 2*175/10
First Posted: June 12, 2014    Key Record Dates
Last Update Posted: May 17, 2016
Last Verified: May 2016
Additional relevant MeSH terms:
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Coronary Artery Disease
Myocardial Infarction
Infarction
Ischemia
Pathologic Processes
Necrosis
Coronary Disease
 Myocardial Ischemia
Heart Diseases
Cardiovascular Diseases
Arteriosclerosis
Arterial Occlusive Diseases
Vascular Diseases