Higher Intensity Interval Training in Cardiac Rehabilitation (HIIT)

This study is ongoing, but not recruiting participants.
Sponsor:
Information provided by (Responsible Party):
Steven J. Keteyian, Henry Ford Health System
ClinicalTrials.gov Identifier:
NCT01606696
First received: May 24, 2012
Last updated: March 18, 2013
Last verified: March 2013

May 24, 2012
March 18, 2013
August 2011
July 2013   (final data collection date for primary outcome measure)
Cardiovascular fitness [ Time Frame: 10 weeks ] [ Designated as safety issue: Yes ]
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
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (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.
 
Active, not recruiting
94
July 2013
July 2013   (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
Both
18 Years to 75 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01606696
HFHS-PC-HIIT
No
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
March 2013

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