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Evaluation of Multi-modal Supportive Actions in Outpatient Cardiac Rehabilitation in Subjects With Cardiovascular Disease

Auswertung Von Multi-modalen unterstützenden Maßnahmen in Der Ambulant Kardiologischen Rehabilitation Bei Patienten Mit Einer kardiovaskulären Erkrankung

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04458727
Acronym
EPICURE
Enrollment
150
Registered
2020-07-07
Start date
2019-12-10
Completion date
2020-09-09
Last updated
2020-07-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Evaluation of Multi-modal Supportive Actions in Outpatient Cardiac Rehabilitation in Subjects With Cardiovascular Disease

Keywords

rehabilitation, cardiovascular disease, outpatient cardiac rehabilitation

Brief summary

Cariovascular diseases (CVD) are the most common cause of death worldwide with high micro- as well as macro-economic burden. Several modifiable risk factors increase the probability of contracting a CVE. These risk factors can be positively influenced by a cardiac rehabilitation measure (CR), which has been shown to reduce mortality in CVD patients and to reduce the economic burden. An increase in physical activity and performance are central goals in CR, as they have a positive effect on several cardiovascular risk factors and correlate strongly with a reduction in mortality in CVD patients. These goals can be achieved in most CVD patients but can only be achieved by a modification of lifestyle. In order to positively influence this lifestyle modification beyond the duration of the CR measure and thus in the long term, CR Phase II should begin as soon as the patient fulfils one of the well-defined inclusion criteria. CR Phase II can be carried out as an inpatient or outpatient procedure and depends on the patient's state of health, personal preference and availability of an outpatient CR facility in the vicinity of the patient. In the Austrian healthcare system, inpatient CR and thus differs from other European countries. After completion of phase II, the patient is offered an outpatient phase III with weekly visits to the outpatient CR facility, so that lifestyle changes achieved at short notice can be sustainably maintained. For the secondary prevention of the CVD beyond the CR measure recommend international guidelines a physical activity of ≥ 150 min with moderate intensity or ≥ 60 to 75 min high intensity per week. The current study situation allows the statement that a greater benefit can be expected from more physical activity and that the training should be personalized and highly titrated. Patients in advanced stages of CVD and very inactive patients, defined as \<14 mets h/week, achieve the greatest health benefit from increased physical activity. Despite the well-studied benefits, even adherence to the above minimum recommendations for CVD patients after completion of CR is low. This deficit has been addressed in the latest European prevention guideline and recommended that patients i) set clearly defined goals, ii) exercise in the iii) Identify obstacles on the way to achieving the goals so that lifestyle changes are effective and sustainable and the benefits of physical activity can be achieved and maintained. The planned study will investigate the effect of multi-modal support measures to help patients during the home training phase and their influence on the patients' lifestyle.

Interventions

None listed

Sponsors

Cardiomed Kardiologisches Rehabilitationszentrum GmbH Linz
CollaboratorUNKNOWN
PKA Private Krankenanstalt Wels Betriebs Gesellschaft mit b. H.
CollaboratorUNKNOWN
Gemeinnützige Salzburger Landeskliniken Betriebsgesellschaften
CollaboratorUNKNOWN
Medreha GmbH
CollaboratorUNKNOWN
ZARG - Zentrum für ambulante Rehabilitation Graz GmbH
CollaboratorUNKNOWN
REHAmed-tirol GmbH Innsbruck
CollaboratorUNKNOWN
Universität Innsbruck
CollaboratorUNKNOWN
AIT Austrian Institute of Technology GmbH
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* Age \>= 18 years * Participation rehabilitation phase III new * Documented cardiovascular disease * Signed informed-consent

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frame
The change of maximal workload during ergometry pre and post home-training1 year

Countries

Austria

Contacts

Primary ContactAngelika Rzepka, MSc
angelika.rzepka@ait.ac.at0043 664 8561598
Backup ContactDieter Hayn, Dr.
dieter.hayn@ait.ac.at0043 50550 2953

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026