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Higher Intensity Interval Training in Cardiac Rehabilitation (HIIT)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01606696
First Posted: May 28, 2012
Last Update Posted: July 16, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Steven J. Keteyian, Henry Ford Health System
  Purpose
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.

Condition Intervention
CAD Behavioral: HIIT Behavioral: Standard intensity non-interval training

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Supportive Care
Official Title: Practical Use of Higher Intensity Interval Exercise in Cardiac Rehabilitation to Improve Aerobic Fitness

Resource links provided by NLM:


Further study details as provided by Steven J. Keteyian, Henry Ford Health System:

Primary Outcome Measures:
  • Cardiovascular fitness [ Time Frame: 10 weeks ]

Enrollment: 49
Study Start Date: August 2011
Study Completion Date: January 2014
Primary Completion Date: November 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: HIIT
Higher intensity interval training.
Behavioral: HIIT
Higher intensity interval training.
Active Comparator: Standard intensity non-interval training
Standard intensity non-interval training
Behavioral: Standard intensity non-interval training
Standard intensity non-interval training.

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 75 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

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
  Contacts and Locations
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): NCT01606696


Locations
United States, Michigan
Henry Ford Health System
Detroit, Michigan, United States, 48202
Sponsors and Collaborators
Henry Ford Health System
Investigators
Principal Investigator: Steven J Keteyian, PhD Henry Ford Health System
  More Information

Responsible Party: Steven J. Keteyian, Program Director, Henry Ford Health System
ClinicalTrials.gov Identifier: NCT01606696     History of Changes
Other Study ID Numbers: HFHS-PC-HIIT
First Submitted: May 24, 2012
First Posted: May 28, 2012
Last Update Posted: July 16, 2015
Last Verified: July 2015

Keywords provided by Steven J. Keteyian, Henry Ford Health System:
CAD
cardiac rehabilitation
fitness