BeSingCardioRehab: CR in Belgium Versus Singapore

Last updated: February 8, 2021
Sponsor: Hasselt University
Overall Status: Completed

Phase

N/A

Condition

Coronary Artery Disease

Thrombosis

Vascular Diseases

Treatment

N/A

Clinical Study ID

NCT03303781
BeSingCardioRehab01
  • Ages > 18
  • All Genders

Study Summary

Background: Cardiac rehabilitation is indicated for ischemic heart disease patients; the program content of which is well described in both European and American guidelines. In contrast, literature on cardiac rehabilitation program content and efficacy in the Asian population is sparse.

Methods: BeSingCardioRehab will be an intercontinental, retrospective cohort study conducted in two cardiac rehabilitation referral centers in Belgium and Singapore. The first aim is to compare the impact of phase II center-based cardiac rehabilitation on Major Adverse Cardiac Events for ischemic heart disease patients between Europe (i.e. Belgian) and Asia (i.e. Singaporean) in the long-term. The second objective is to compare the efficacy of phase II cardiac rehabilitation on short-term morbidity (assessed with the validated SMART Risk Score) between index European and Asian ischemic heart disease patients. The level of compliance of the Belgian and Singaporean cardiac rehabilitation programs to European guidelines standards will also be evaluated.

Hypotheses BeSingCardiorehab will be one of the first studies assessing cardiac rehabilitation in Asia. Based on the BeSingCardioRehab study results, phase II center-based cardiac rehabilitation programs, can/will be adapted in order to improve program content and outcomes.

Eligibility Criteria

Inclusion

Inclusion Criteria: i. patients in the revascularised, stabilized and asymptomatic phase following an acutecoronary syndrome (ACS) (unstable angina, non ST-elevation ACS or ST-elevation ACS) ii. patients initially presenting with stable angina who are revascularised or asymptomaticunder optimal medical treatment (not amenable for revascularization).

Exclusion

Exclusion Criteria: i. end-stage chronic kidney disease (stage V, GFR < 15 ml/min/1.73 m2 and/or dialysis) ii.severe chronic obstructive pulmonary disease (COPD) (GOLD stage III-IV, Tiffeneau index < 0.70 and FEV1 < 49% of normal) iii. terminal cancer with a prognosis of < 1 year.

Study Design

Total Participants: 2792
Study Start date:
April 01, 2018
Estimated Completion Date:
January 01, 2021

Study Description

BeSingCardioRehab is an intercontinental, multi-center, retrospective cohort study conducted in two cardiac rehabilitation referral centers (Heart Center Hasselt in Belgium and National Heart Center Singapore in Singapore).

Patients will be divided in four groups (1:1:1:1) based on i. whether or not they received phase II cardiac rehabilitation and ii. whether they are from Belgium or Singapore.

The first objective of BeSingCardioRehab is to compare the impact of phase II center-based cardiac rehabilitation on Major Adverse Cardiac Events for ischemic heart disease patients between Europe (i.e. Belgian) and Asia (i.e. Singaporean) in the long-term. The second objective is to compare the efficacy of phase II cardiac rehabilitation on short-term morbidity (assessed with the validated SMART Risk Score) between index European and Asian ischemic heart disease patients. The level of compliance of the Belgian and Singaporean cardiac rehabilitation programs to European guidelines standards will also be evaluated.

Connect with a study center

  • Jessa Hospital

    Hasselt, 3500
    Belgium

    Site Not Available

  • National Heart Center Singapore

    Singapore,
    Singapore

    Site Not Available

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