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NCT01606696 Clinical Trial

Higher Intensity Interval Training in Cardiac Rehabilitation

CAD Clinical Trial

— HIIT  

Official title:
Practical Use of Higher Intensity Interval Exercise in Cardiac Rehabilitation to Improve Aerobic Fitness

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01606696
Other study ID # HFHS-PC-HIIT
Secondary ID
Status Completed
Phase N/A
First received May 24, 2012
Last updated July 15, 2015
Start date August 2011
Est. completion date January 2014

Study information
Verified date July 2015
Source Henry Ford Health System
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Completed
Enrollment 49
Est. completion date January 2014
Est. primary completion date November 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility 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

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Supportive Care

Related Conditions & MeSH terms

Intervention

Behavioral:
• HIIT
Higher intensity interval training.
• Standard intensity non-interval training
Standard intensity non-interval training.

Locations
Country Name City State
United States Henry Ford Health System Detroit Michigan

Sponsors (1)
Lead Sponsor Collaborator
Henry Ford Health System

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Cardiovascular fitness 10 weeks Yes
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