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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01453166
Other study ID # 01/2011
Secondary ID
Status Completed
Phase N/A
First received October 11, 2011
Last updated July 16, 2012
Start date September 2011
Est. completion date January 2012

Study information

Verified date July 2012
Source Hospital do Coracao
Contact n/a
Is FDA regulated No
Health authority Brazil: Ethics Committee
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the effectiveness of a brazilian cardioprotective diet plan to reduce cardiovascular risk factors of new cardiovascular events.


Description:

Cardiovascular diseases are the leading cause of mortality in both sexes in Brazil and worldwide. Modifying risk factors such as diet and lifestyle can prevent most cases of cardiovascular disease. This pilot trial is based on specific and traditional brazilian food. The objective is to reduce risk factors such as obesity, high blood pressure,dyslipidemia and diabetes in patients with cardiovascular disease history.


Recruitment information / eligibility

Status Completed
Enrollment 122
Est. completion date January 2012
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender Both
Age group 45 Years and older
Eligibility Inclusion Criteria:

- Any coronary artery disease evidence in the past 10 years; or any ischemic stroke or TIA evidence in the past 10 years; or peripheral arterial disease in the past 10 years; or at least one of the following additional risk factors:

- Diabetes Mellitus; Hypertension; Dyslipidemia; Coronary artery disease family history;

- Asymptomatic carotid artery disease;

- Body mass index> 25 kg/m2 for adults and> 28 kg/m2 for seniors

Exclusion Criteria:

- Neurocognitive or psychiatric condition;

- Life expectancy less than 6 months (eg, metastatic malignancy or other defined as clinical trial investigators).

- Pregnancy or breast feeding.

- Hepatic impairment defined as elevated liver enzymes above three times the upper limit of normal

- Renal impairment defined as creatinine values higher than 1.5 mg/dL.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Other:
Brazilian heart-prevent meal
Nutrient profile of the diets used was based on the Brazilian guidelines to cardiovascular disease treatment.The main difference between this group involves a Brazilian version of accessible and energy density concept dietary therapy to cardiovascular diseases. Furthermore, it explores a set of tools and educational materials that help the patient understand and follow the principles of balanced and healthy diet weekly session with the dietitians which could be in person, by phone or in a gourmet shop. During attendances at the gourmet shop, patients received tips for eating in restaurants, instruction on label reading and a list of typical foods. The menus were based on typical foods consumed in Brazil, all foods included in the menu were low-cost and widely available at local markets
Heart prevent control meal weekly
received the usual dietary therapy to patients with cardiovascular diseases, which had the same nutrient profile as presented in Group A, but customized by the integration of mediterranean typical foods (e.g. olive oil and nuts). The difference between groups B and C was the number of sessions with the dietician. Group B received weekly sessions, which could be in person or by phone, and group C had monthly in person sessions
Heart prevent control Meal monthly
received the usual dietary therapy to patients with cardiovascular diseases, which had the same nutrient profile as presented in Group A and B, but customized by the integration of mediterranean typical foods (e.g. olive oil and nuts) at the same of group B. The difference of group C was the number of sessions with the dietician. That happen monthly in person sessions.

Locations

Country Name City State
Brazil Hospital do Coracao Sao Paulo

Sponsors (2)

Lead Sponsor Collaborator
Hospital do Coracao Ministry of Health, Brazil

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Systolic Blood Pressure Change From Baseline in systolic blood pressure 12 weeks Yes
Primary Total Cholesterol Change From Baseline in total Cholesterol 12 weeks Yes
Secondary Weight Change From Baseline in weight 12 weeks Yes
Secondary Waist Circumference Change From Baseline in wais circumference 12 weeks Yes
Secondary Blood Glucose Change From Baseline in blood glucose 12 weeks No
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