SPICE UP MyPlate - Strategy for Promoting Intake of Delicious Healthful Dietary Patterns Based on MyPlate: A Pilot Study

February 9, 2026 updated by: Kristina Petersen PhD, APD, FAHA, Penn State University
The aim is to conduct a pilot study to assess the feasibility, acceptability and potential effectiveness of culinary focused nutrition education to promote increased adherence to the Dietary Guidelines for Americans compared to standard low-intensity care.

Study Overview

Detailed Description

This is a 15-week, 2-arm randomized controlled pilot trial. In a 1:1 ratio, participants will be randomized to the intervention arm or the control arm. The intervention group will receive a 12-week culinary focused nutrition education program. The control group will receive standard low-intensity care (i.e., printed healthy eating material). Outcome measures will be assessed at baseline and 15 weeks.

Study Type

Interventional

Enrollment (Actual)

55

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

    • Pennsylvania
      • University Park, Pennsylvania, United States, 16802
        • Pennsylvania State University

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Age 31-59 years
  • Involved in meal cooking at home and consumes a home cooked meal ≥ 1 time per week
  • Individuals taking medications for blood pressure, lipid or glucose lowering will be eligible if they have been on a stable dose for the 1 month prior to baseline

Exclusion Criteria:

  • A member of the household is already enrolled (only one person per household will be eligible for inclusion in the study).
  • Unstable medical conditions requiring active intervention (surgeries, medication/drug therapy for < 3 months) as assessed during the telephone screening (e.g. cancer, kidney disease requiring dialysis, heart or gastrointestinal diseases requiring surgery).
  • Received nutrition education for a medical condition within the past 6 months
  • Currently following a weight loss diet
  • Lost ≥ 10% body weight in the past 6 months
  • Currently (within 6 months) smoke or use any tobacco or nicotine containing products
  • Currently pregnant or given birth within the prior 6 months
  • Currently participating in another clinical trial
  • Principal investigator discretion (e.g., disrespectful or inappropriate interactions with study staff)
  • Does not speak or understand English

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: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Culinary focused nutrition education
The intervention group will receive a 12-week culinary focused nutrition education program. Participants in the intervention group will receive culinary focused nutrition education based on MyPlate with an emphasis on taste and enjoyment of healthy foods. Using herbs and spices to flavor foods will be the emphasis. The intervention will be delivered in an online format with online content delivery . The intervention will consist of eight modules. Modules one to four will be provided during the first month. Modules four to eight will be provided during months 2 and 3.
Culinary focused nutrition education based on MyPlate with an emphasis on taste and enjoyment of healthy foods.
Active Comparator: Standard nutrition education
The control group will represent standard low intensity nutrition education. Control group participants will be provided with a printed MyPlate resource.
Provided by a written MyPlate resource

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Diet quality change
Time Frame: 15 weeks
Change in diet quality assessed by the Healthy Eating Index-2015 (HEI-2015) assessed by 24-hour recalls
15 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Diet quality component scores change
Time Frame: 15 weeks
Change in the 13 components that comprise the Healthy Eating Index-2015 (HEI-2015) assessed by 24 hour recalls
15 weeks
Food group intake change
Time Frame: 15 weeks
Changes in intake of fruits; vegetables; refined grains; wholegrains; dairy; meat, poultry, eggs; seafood; nuts, seeds and soy products; oils) assessed by 24-hour recalls
15 weeks
Change in intake of added sugars, sodium and saturated fat
Time Frame: 15 weeks
Changes in intake of added sugars, sodium and saturated fat assessed by 24 hour recalls
15 weeks
Change in weight
Time Frame: 15 weeks
assessed by electronic scale
15 weeks
Change in waist circumference
Time Frame: 15 weeks
Assessed by tape measure at 1 cm above the naval
15 weeks
Change in central systolic and diastolic blood pressure
Time Frame: 15 weeks
Assessed using a SphymoCor Xcel (Atcor Medical)
15 weeks
Change in brachial systolic and diastolic blood pressure
Time Frame: 15 weeks
Blood pressure measured assessed using a SphymoCor Xcel (Atcor Medical)
15 weeks
Change in carotid-femoral pulse wave velocity
Time Frame: 15 weeks
Assessed using a SphymoCor Xcel (Atcor Medical)
15 weeks
Change in LDL-cholesterol
Time Frame: 15 weeks
Assessed from fasting blood draw expressed in mg/dL. LDL-cholesterol will be measured directly via enzymatic assay.
15 weeks
Change in total cholesterol
Time Frame: 15 weeks
Assessed from fasting blood draw expressed in mg/dL.
15 weeks
Change in HDL-Cholesterol
Time Frame: 15 weeks
Assessed from fasting blood draw expressed in mg/dL.
15 weeks
Change in triglycerides
Time Frame: 15 weeks
Assessed from fasting blood draw expressed in mg/dL.
15 weeks
Change in fasting glucose
Time Frame: 15 weeks
Assessed in a fasting blood draw and expressed in mg/dL
15 weeks
Change in HbA1c
Time Frame: 15 weeks
Assessed in a fasting blood draw and expressed in %
15 weeks
Program acceptability and satisfaction
Time Frame: 15 weeks
Assessed via surveys
15 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Kristina Petersen, PhD, Penn State University

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 28, 2025

Primary Completion (Actual)

December 12, 2025

Study Completion (Actual)

December 12, 2025

Study Registration Dates

First Submitted

March 17, 2025

First Submitted That Met QC Criteria

March 17, 2025

First Posted (Actual)

March 24, 2025

Study Record Updates

Last Update Posted (Actual)

February 12, 2026

Last Update Submitted That Met QC Criteria

February 9, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • SUP

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Sharing Time Frame

Statistical analysis plan will be uploaded before database lock and unblinding of randomization codes

IPD Sharing Supporting Information Type

  • SAP

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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