More Intensive Cardiac Rehabilitation Programs in Less Time
- 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
- 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
- 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
Group Intervention Description Intensivo Intensive cardiac rehabilitation program in less time intensive cardiac rehabilitation program in less time
- Primary Outcome Measures
Name Time Method Number of participants reporting compliance with prescribed treatments baseline-12 months Patient-reported answers form the investigator
Adherence to physical exercise baseline-12 months Assessed in Metabolic Equivalents of Task (METS) from baseline by ergometry
Adherence to Mediterranean diet baseline-12 months Assessed by Mediterranean diet adherence questionnaire (Modified Trichopoulou A,)
Tabacco abstinence baseline-12 months Assessed by cooximetry (less dan 10 ppm)
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Hospital Universitario La Paz
🇪🇸Madrid, Spain