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Diet and Prevention of Ischemic Heart Disease: a Translational Approach

Not Applicable
Completed
Conditions
Ischemic Heart Disease
Interventions
Other: DIPI
Registration Number
NCT02062424
Lead Sponsor
Technical University of Denmark
Brief Summary

The objective of this study is to test the effect of substitution dietary guidelines that are specifically aimed at the prevention of ischemic heart disease (IHD) on the dietary intake in the general Danish population.

Detailed Description

225 participants will be included in the intervention. The intervention is planned to run for six months in a real life setting.

The study is a randomized, parallel dietary intervention study. Dietary intake, selected IHD biomarkers and anthropometric measurements will be measured at two visits during the intervention period as well as 6 months after the end of the intervention. The study includes a baseline visit followed by a visit where web based dietary records will be completed by the subjects and blood samples and anthropometrics will be measured.

The intervention will consist of information on dietary advice due to the specific IHD dietary guideline or the current national dietary guidelines. The information will be provided to the participants via leaflets and recipes.

After the baseline visit the subjects will be randomized to group A, B or C: In group A the subjects will receive dietary advice, according to the specific IHD dietary guideline, in group B the subjects will receive dietary advice according to the current national dietary guidelines and in group C the subjects will be instructed to follow their normal dietary habits.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
222
Inclusion Criteria
  • healthy men and women aged 30 to 65 years who has one or more self-assessed ischemic heart disease risk factors at screening: physical inactivity, overweight or obese (BMI ≥ 25/m2 ), waist circumference (≥ 80 cm for women, ≥ 94 cm for men). In addition, the participants should have the motivation and willingness to be randomized to any of the three groups, and to do their best to follow the given protocol .
Exclusion Criteria
  • no internet access or no access to a computer, smoking, pregnancy, or breast-feeding or planning to become pregnant within the next 12 months, a history of cardiovascular disease, type 2 diabetes, chronic disease / disorders that may affect the results of the study, substance abuse within the past 12 months, regular alcohol consumption > 21 units / week for men or > 14 units/ week for women, allergy or intolerance to food groups in the dietary guidelines, supplements with mega doses of nutrients that can have potential impact on ischemic heart disease risk markers (eg . fish oils).

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
DIPI: Danish national dietary guidelinesDIPIThe subjects will receive dietary advice according to the current national dietary guidelines
DIPI: Specific IHD dietary guidelineDIPIThe subjects will receive dietary advice, according to the specific ischemic heart disease dietary guidelines.
Primary Outcome Measures
NameTimeMethod
Dietary intake6 month

Dietary intake will be measured at two visits during the intervention period as well as 6 months after the end of the intervention.

Secondary Outcome Measures
NameTimeMethod
Selected ischemic heart disease biomarkers and anthropometric measurements6 month

Selected IHD biomarkers and anthropometric measurements will be measured at two visits during the intervention period as well as 6 months after the end of the intervention.

Trial Locations

Locations (1)

Technical University of Denmark

🇩🇰

Søborg, Denmark

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