Ischemic Heart Disease Clinical Trial
Official title:
The CardioDiet Trial
This is a multi-centre, open, randomised study in patients treated for ischemic heart disease in Linköping, Norrköping and Jönköping hospitals. One thousand two hundred patients who are treated at the cardiac rehabilitation units will be consecutively recruited during three years. The patients will be randomised 1:1 to be given advice on a 1) Mediterranean diet with an energy content (E%) from carbohydrates between 25-30% or to 2) a traditional low-fat diet with 45-60 E% from carbohydrates. All eligible patients will be asked if they want to participate and provided with written information about the study when they are discharged from the hospital after treatment for ischemic heart disease. The decision to participate or not will be given at the following outpatient treatment at the cardiac rehabilitation unit. When the signed informed consent to participate in the study has been provided, the patient will be randomised to advice of either of the two dietary regimes.
Aim To compare advice on a Mediterranean diet with an energy content (E%) from carbohydrates
between 25-30 E% with a traditional low-fat diet with 45-60 E% from carbohydrates.
Primary outcome Incidence of diabetes in non-diabetic patients or glycaemic control in
patients with known diabetes.
Secondary outcome Recurrence of cardiovascular disease, blood lipid levels, quality of life
by questionnaires.
Study design and study population This is a multi-centre, open, randomised study in patients
treated for ischemic heart disease in Linköping, Norrköping and Jönköping hospitals. One
thousand two hundred patients who are treated at the cardiac rehabilitation units will be
consecutively recruited during three years. The patients will be randomised 1:1 to be given
advice on a 1) Mediterranean diet with an energy content (E%) from carbohydrates between
25-30% or to 2) a traditional low-fat diet with 45-60 E% from carbohydrates. All eligible
patients will be asked if they want to participate and provided with written information
about the study when they are discharged from the hospital after treatment for ischemic heart
disease. The decision to participate or not will be given at the following outpatient
treatment at the cardiac rehabilitation unit. When the signed informed consent to participate
in the study has been provided, the patient will be randomised to advice of either of the two
dietary regimes.
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