Higher Intensity Interval Training in Cardiac Rehabilitation

NCT ID: NCT01606696

Last Updated: 2015-07-16

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

49 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-08-31

Study Completion Date

2014-01-31

Brief Summary

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The purpose of this study is to compare the effect higher intensity interval exercise (HIIT) with standard intensity non-interval exercise on fitness in cardiac rehabilitation patients with CAD. Also to assess practical implementation of HIIT in cardiac rehabilitation.

Detailed Description

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Conditions

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CAD

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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HIIT

Higher intensity interval training.

Group Type EXPERIMENTAL

HIIT

Intervention Type BEHAVIORAL

Higher intensity interval training.

Standard intensity non-interval training

Standard intensity non-interval training

Group Type ACTIVE_COMPARATOR

Standard intensity non-interval training

Intervention Type BEHAVIORAL

Standard intensity non-interval training.

Interventions

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HIIT

Higher intensity interval training.

Intervention Type BEHAVIORAL

Standard intensity non-interval training

Standard intensity non-interval training.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Age 18-75 years
* Male or female
* Angiographic documentation of CAD

Exclusion Criteria

* Unstable angina pectoris
* MI / PCI \< 3 weeks
* CABG \< 4weeks
* Exercise induced ischemia \> 1mm ST depression
* LVEF \< 40%
* complex ventricular arrhythmias or atrial fibrillation
* orthopedic limitations to treadmill exercise
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Henry Ford Health System

OTHER

Sponsor Role lead

Responsible Party

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Steven J. Keteyian

Program Director

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Steven J Keteyian, PhD

Role: PRINCIPAL_INVESTIGATOR

Henry Ford Health System

Locations

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Henry Ford Health System

Detroit, Michigan, United States

Site Status

Countries

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United States

Other Identifiers

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HFHS-PC-HIIT

Identifier Type: -

Identifier Source: org_study_id

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