We updated the design of this site on September 25th. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

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
May 24, 2012
May 28, 2012
July 16, 2015
August 2011
November 2012   (Final data collection date for primary outcome measure)
Cardiovascular fitness [ Time Frame: 10 weeks ]
Same as current
Complete list of historical versions of study NCT01606696 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Higher Intensity Interval Training in Cardiac Rehabilitation
Practical Use of Higher Intensity Interval Exercise in Cardiac Rehabilitation to Improve Aerobic Fitness
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.
Not Provided
Interventional
Not Provided
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Supportive Care
CAD
  • Behavioral: HIIT
    Higher intensity interval training.
  • Behavioral: Standard intensity non-interval training
    Standard intensity non-interval training.
  • Experimental: HIIT
    Higher intensity interval training.
    Intervention: Behavioral: HIIT
  • Active Comparator: Standard intensity non-interval training
    Standard intensity non-interval training
    Intervention: Behavioral: Standard intensity non-interval training
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
49
January 2014
November 2012   (Final data collection date for primary outcome measure)

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
Sexes Eligible for Study: All
18 Years to 75 Years   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT01606696
HFHS-PC-HIIT
No
Not Provided
Not Provided
Steven J. Keteyian, Henry Ford Health System
Henry Ford Health System
Not Provided
Principal Investigator: Steven J Keteyian, PhD Henry Ford Health System
Henry Ford Health System
July 2015

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP