Outpatient Cardiac Rehabilitation in Austria

This study is currently recruiting participants. (see Contacts and Locations)
Verified April 2014 by Paracelsus Medical University
Sponsor:
Information provided by (Responsible Party):
Prof. Josef Niebauer M.D., Ph.D., MBA, Paracelsus Medical University
ClinicalTrials.gov Identifier:
NCT01540006
First received: February 22, 2012
Last updated: April 24, 2014
Last verified: April 2014
  Purpose

The aim of this prospective trial is the manifestation of guidelines developed for outpatient cardiac rehabilitation in Austria.

The evaluation of prospective and retrospective data is supposed to give evidence on morbidity and/or mortality advantages compared to patients not participating in cardiac rehabilitation programs.

The database created in this context is supposed to pave the way as instrument to document and comprehend quality and cost effectiveness of outpatient cardiac rehabilitation in Austria as a key for quality management.


Condition Intervention
Heart Disease
Other: Physical activity

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective

Resource links provided by NLM:


Further study details as provided by Paracelsus Medical University:

Primary Outcome Measures:
  • Physical work capacity (PWC) [ Time Frame: 6 weeks ] [ Designated as safety issue: No ]
    PWC is measuered by gradded exercise test on cycling ergometer before and after rehabilitation.


Estimated Enrollment: 1000
Study Start Date: January 2009
Estimated Primary Completion Date: December 2015 (Final data collection date for primary outcome measure)
Intervention Details:
    Other: Physical activity
    50min of endurance training combined with 45min of calisthenics; 1-3x/week; 6-24 weeks
  Eligibility

Ages Eligible for Study:   18 Years to 90 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Any patients with heart disease willing to participate in an ambulant cardiac rehabilitation.

Criteria

Inclusion Criteria:

  • heart disease

Exclusion Criteria:

  • participation in another study within the previous 6 months
  • Medical conditions which prevent patients from complying with the exercise program
  • Acute infections
  • Hypertrophic cardiomyopathy
  • Pulmonary artery embolism or phlebothrombosis within the previous 6 months
  • Unstable angina pectoris
  • Heart failure (NYHA IV)
  • Hemodynamically unstable arrhythmia
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01540006

Contacts
Contact: Prof. Josef Niebauer, MD, PhD, MBA 00436624482 ext 4270 j.niebauer@salk.at

Locations
Austria
Department of Sports Medicine, Prevention and Rehabilitation Paracelsus Medical University Recruiting
Salzburg, Austria, 5020
Contact: Prof. Josef Niebauer, MD, PhD, MBA    00436624482 ext 4270    j.niebauer@salk.at   
Sponsors and Collaborators
Paracelsus Medical University
Investigators
Study Chair: Prof. Josef Niebauer, MD, PhD, MBA Paracelsus Medical University
  More Information

Additional Information:
Publications:
Responsible Party: Prof. Josef Niebauer M.D., Ph.D., MBA, Head of institute, Paracelsus Medical University
ClinicalTrials.gov Identifier: NCT01540006     History of Changes
Other Study ID Numbers: UISM-6
Study First Received: February 22, 2012
Last Updated: April 24, 2014
Health Authority: Austria: Ethikkommission

Additional relevant MeSH terms:
Heart Diseases
Cardiovascular Diseases

ClinicalTrials.gov processed this record on September 30, 2014