NCT02162290

Brief Summary

The research will study the differences between interval training and continuous training among cardiac patients in a cardiac rehabilitation facility. The main objectives are:

  1. 1.Functional capacity measures (VO2 max).
  2. 2.Cardiac risk factors
  3. 3.Quality of life assessments.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
84

participants targeted

Target at P25-P50 for not_applicable coronary-artery-disease

Timeline
Completed

Started May 2011

Typical duration for not_applicable coronary-artery-disease

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2011

Completed
3.1 years until next milestone

First Submitted

Initial submission to the registry

June 11, 2014

Completed
1 day until next milestone

First Posted

Study publicly available on registry

June 12, 2014

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2015

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2015

Completed
Last Updated

May 17, 2016

Status Verified

May 1, 2016

Enrollment Period

4 years

First QC Date

June 11, 2014

Last Update Submit

May 15, 2016

Conditions

Coronary Artery DiseaseMyocardial Infarction

Outcome Measures

Primary Outcomes (1)

  • Maximal functional capacity

    Outcome is assessed at baseline, after 3 months and at nine months

    9 months

Study Arms (2)

Interval exercise

EXPERIMENTAL

Exercise bouts in low and high intensities

Other: Interval exercise training

Continuous exercise

EXPERIMENTAL

Exercise continuously with moderate intensity

Other: Continuous exercise training

Interventions

Interval exercise trainingOTHER

Exercise bouts in low and high intensities

Interval exercise
Continuous exercise trainingOTHER
Continuous exercise

Eligibility Criteria

Age40 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Patients undergone:
  • Myocardial infarction
  • Percutaneous transluminal coronary angioplasty
  • Coronary artery bypass graft

You may not qualify if:

  • Patients with:
  • Severe ischemia or angina
  • Implantable cardioverter-defibrillator
  • Pacemakers transplants
  • Severe left ventricular dysfunctions
  • Uncontrolled arrhythmias

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Asaf Harofe Medical Center

Beer Yaacov, Israel

Location

MeSH Terms

Conditions

Coronary Artery DiseaseMyocardial Infarction

Condition Hierarchy (Ancestors)

Coronary DiseaseMyocardial IschemiaHeart DiseasesCardiovascular DiseasesArteriosclerosisArterial Occlusive DiseasesVascular DiseasesInfarctionIschemiaPathologic ProcessesPathological Conditions, Signs and SymptomsNecrosis

Study Officials

  • Yael Pernick

    Asaf Harofe Medical Center

    PRINCIPAL INVESTIGATOR

  • Zyssman, MD

    Asaf Harofe Medical Center

    STUDY DIRECTOR

  • Jonathan Moore, PhD

    Bangor University

    STUDY DIRECTOR

  • Zvi Vered, MD

    Asaf Harofe Medical Center

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER GOV
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 11, 2014

First Posted

June 12, 2014

Study Start

May 1, 2011

Primary Completion

May 1, 2015

Study Completion

May 1, 2015

Last Updated

May 17, 2016

Record last verified: 2016-05

Locations

IL(1)