- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05180435
Dietary Approaches for Cardiovascular Health Study
March 17, 2025 updated by: University of Delaware
Family Meals as a Strategy for the Primary Prevention of Cardiovascular Disease in Children
The primary purpose of this study is to examine the efficacy of family meal frequency as an intervention target in addressing the primary prevention of CVD.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
42
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Delaware
-
Newark, Delaware, United States, 19713
- University of Delaware, Energy Balance and Nutrition Laboratory
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
6 years to 12 years (Child)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Parents who have a male or female child aged 6-12 years-old with a BMI-for-sex and age <95th percentile
- Parent age is ≥18 years-old
- Parent reports at least 2 of the following CVD risk factors: smoking, high cholesterol, high blood pressure, physical inactivity, overweight/obesity, diabetes
- Parent is able to read, speak and understand English
Exclusion Criteria:
- Parents who live with their child <5 days per week
- Parents who do not have access to the internet and/or are unable to attend intervention sessions
- Parents who report a medical condition that impacts growth or requires a specific eating plan for themselves or their child.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Family Meals
Have at least 5 dinners per week.
|
A family-based multicomponent lifestyle modification intervention with the goal to increase the frequency of family meals and meet physical activity recommendations.
|
|
Active Comparator: Standard
Consume the recommended amounts of fruits and vegetables.
|
A family-based multicomponent lifestyle modification intervention with the goal to increase the consumption of fruits and vegetables and and meet physical activity recommendations.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline in diet quality.
Time Frame: Baseline and Months 2, 6, 8 and 10
|
The Healthy Eating Index is a score ranging from 0-100 with higher scores indicating greater adherence to the Dietary Guidelines.
|
Baseline and Months 2, 6, 8 and 10
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline in body mass index z-scores (zBMI)
Time Frame: Baseline and Months 2, 6, 8 and 10
|
Body mass index z-scores (zBMI) will be calculated using Centers for Disease Control and Prevention growth charts.
Height will be measured in centimeters and weight will be measured in kilograms and used to calculate BMI as kilograms/meter squared.
|
Baseline and Months 2, 6, 8 and 10
|
|
Change from baseline in blood pressure
Time Frame: Baseline and Month 6
|
Both systolic and diastolic blood pressure.
|
Baseline and Month 6
|
|
Change from baseline in fasting insulin
Time Frame: Baseline and Month 6
|
Measure of insulin in the blood after fasting.
|
Baseline and Month 6
|
|
Change from baseline in fasting glucose
Time Frame: Baseline and Month 6
|
Measure of blood sugar (glucose) after fasting.
|
Baseline and Month 6
|
|
Change from baseline in lipid levels
Time Frame: Baseline and Month 6
|
Nuclear magnetic resonance (NMR) measures of lipoprotein (low-density lipoprotein [LDL], high-density lipoprotein [HDL], very-low density lipoprotein [VLDL]) particle number and size will be assessed.
|
Baseline and Month 6
|
|
Change from baseline in pulse wave analysis.
Time Frame: Baseline and Month 6
|
PWA will be assessed by a central aortic pressure waveform synthesized from the measured brachial artery pressure waveform via a standard blood pressure cuff inflation/deflation and blood pressure monitoring.
|
Baseline and Month 6
|
|
Change from baseline in carotid-to-femoral pulse wave velocity (PVW)
Time Frame: Baseline and Month 6
|
Carotid-to-femoral PWV will be measured by simultaneously recording electrocardiography (ECG) and a carotid or femoral pressure waveform via a standard blood pressure cuff inflation/deflation and blood pressure monitoring.
The distance from the carotid measurement point to the sternal notch will be subtracted from the distance from the sternal notch to the femoral measurement point and used as propagation distance.
PWV will be calculated as propagation distance/time delay.
PWV is a measure of regional stiffness of the aorta.
|
Baseline and Month 6
|
|
Change in baseline in flow-mediated dilation (FMD)
Time Frame: Baseline and Month 6
|
The FMD technique will be employed by assessing the diameter and blood flow velocity of the artery located in the upper arm via ultrasonography.
FMD will be used as a measure of endothelial-dependent vessel function and will be expressed as a percent change from baseline, normalized for shear rate calculated from blood flow velocity and vessel diameter data.
|
Baseline and Month 6
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 15, 2022
Primary Completion (Estimated)
May 31, 2025
Study Completion (Estimated)
May 31, 2025
Study Registration Dates
First Submitted
December 6, 2021
First Submitted That Met QC Criteria
December 17, 2021
First Posted (Actual)
January 6, 2022
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
March 17, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1761471
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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