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

NCT ID: NCT02162290

Last Updated: 2016-05-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

84 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-05-31

Study Completion Date

2015-05-31

Brief Summary

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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.

Detailed Description

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Conditions

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Coronary Artery Disease Myocardial Infarction

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Interval exercise

Exercise bouts in low and high intensities

Group Type EXPERIMENTAL

Interval exercise training

Intervention Type OTHER

Exercise bouts in low and high intensities

Continuous exercise

Exercise continuously with moderate intensity

Group Type EXPERIMENTAL

Continuous exercise training

Intervention Type OTHER

Interventions

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Interval exercise training

Exercise bouts in low and high intensities

Intervention Type OTHER

Continuous exercise training

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

40 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Assaf-Harofeh Medical Center

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Yael Pernick

Role: PRINCIPAL_INVESTIGATOR

Asaf Harofe Medical Center

Zyssman, MD

Role: STUDY_DIRECTOR

Asaf Harofe Medical Center

Jonathan Moore, PhD

Role: STUDY_DIRECTOR

Bangor University

Zvi Vered, MD

Role: STUDY_DIRECTOR

Asaf Harofe Medical Center

Locations

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Asaf Harofe Medical Center

Beer Yaacov, , Israel

Site Status

Countries

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Israel

Other Identifiers

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2*175/10

Identifier Type: -

Identifier Source: org_study_id

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