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More Intensive Cardiac Rehabilitation Programs in Less Time

Not Applicable
Completed
Conditions
Acute Coronary Syndrome
Interventions
Other: Intensive cardiac rehabilitation program in less time
Registration Number
NCT02619422
Lead Sponsor
Almudena Castro Conde
Brief Summary

To determine if an intensive cardiac rehabilitation program with periodic reinforcements improve the compliance/adherence to secondary preventive measures (physical exercise, mediterranean diet, tobacco abstinence, pharmacological treatment) after an acute coronary syndrome with or without ST segment elevation versus an standard cardiac rehabilitation program

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
509
Inclusion Criteria
  • Signed informed consent
  • Equal or older 18 years old
  • Acute coronary syndrome with or without ST elevation within last two months
  • Being able to do physical exercise
  • Being able to understand the educative sessions
  • Being able to understand patient information in the consent form
Exclusion Criteria
  • Hemodynamic instability
  • Left ventricular ejection fraction (LVEF) < or = 35%
  • Heart failure class III -IV (New York Heart Association (NYHA) Functional Classification)
  • Refractory angina
  • Any pathology for which physical exercise is not indicated

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
IntensivoIntensive cardiac rehabilitation program in less timeintensive cardiac rehabilitation program in less time
Primary Outcome Measures
NameTimeMethod
Number of participants reporting compliance with prescribed treatmentsbaseline-12 months

Patient-reported answers form the investigator

Adherence to physical exercisebaseline-12 months

Assessed in Metabolic Equivalents of Task (METS) from baseline by ergometry

Adherence to Mediterranean dietbaseline-12 months

Assessed by Mediterranean diet adherence questionnaire (Modified Trichopoulou A,)

Tabacco abstinencebaseline-12 months

Assessed by cooximetry (less dan 10 ppm)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Hospital Universitario La Paz

🇪🇸

Madrid, Spain

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