- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04240782
Market to MyPlate: Investigating the Impact of a Nutrition and Hands-On Cooking Intervention
January 21, 2020 updated by: University of Illinois at Urbana-Champaign
Market to MyPlate: A Cluster Randomized Trial Investigating the Impact of a Nutrition and Hands-On Cooking Intervention on Dietary, Cooking, and Shopping Behaviors
Recent peer-reviewed research indicates that low-income families are at higher risk for unhealthy dietary intake and associated poor health outcomes.
Interventions that teach individuals from low-income families about cooking and healthy eating are warranted to improve overall dietary behaviors.
The purpose of this study is to evaluate the impact of the Market to MyPlate Program on participants' reported cooking, shopping, and dietary behaviors using a cluster randomized trial design, where class cohorts are randomly assigned to education with produce allocations, education only, or control conditions.
A secondary aim is to collect program feedback and better understand facilitators and barriers to farmer's market use and food waste reduction.
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
120
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
-
-
Illinois
-
Urbana, Illinois, United States, 61801
- University of Illinois
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Recruited from SNAP-Ed eligible site (site where the majority of participants are eligible for US food assistance programs)
- Must be 18 years or older, or parent of any age with child(ren) to participate in data collection (all ages including children could participate in intervention)
Exclusion Criteria:
• Participated in an Extension nutrition education program in the last year
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: Education with Produce Allocations
Participants will attend nutrition education and hands-on cooking classes with weekly produce allocations from a local farm.
|
The adults and children will learn how to prepare the fresh produce during an age appropriate, evidence-based, family cooking school.
The class will provide participants with a no-cost, low-risk incentive to try new vegetables, and will empower them to build healthier lives through nutrient-rich, locally sourced meals.
Participants will also receive nutrition education and information on how they can integrate local produce into their food budget.
One of the class sessions will focus solely on how to budget for healthy food, comparison shop, and make the most of their food dollars.
Participants will learn how to use their SNAP benefits at local farmers markets.
Participants will also receive a produce allocation from a local farm during each session of the class.
|
Experimental: Education only
Participants will attend nutrition education and hands-on cooking classes (with produce coupons provided after intervention).
|
The adults and children will learn how to prepare the fresh produce during an age appropriate, evidence-based, family cooking school.
The class will provide participants with a no-cost, low-risk incentive to try new vegetables, and will empower them to build healthier lives through nutrient-rich, locally sourced meals.
Participants will also receive nutrition education and information on how they can integrate local produce into their food budget.
One of the class sessions will focus solely on how to budget for healthy food, comparison shop, and make the most of their food dollars.
Participants will learn how to use their SNAP benefits at local farmers markets.
|
No Intervention: Control group
Participants will receive a delayed intervention once the study period is over.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Self-reported vegetable consumption
Time Frame: 7 weeks
|
Survey asks participants to self-report how frequently they consume fruits and vegetables.
|
7 weeks
|
self-reported shopping behaviors
Time Frame: 7 weeks
|
Survey asks participants to self-report how frequently they compare food prices, make shopping lists, and plan meals before grocery shopping.
|
7 weeks
|
self-reported cooking behaviors
Time Frame: 7 weeks
|
Survey asks participants to self-report how frequently they cook dinner at home.
|
7 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
June 11, 2018
Primary Completion (Actual)
November 1, 2018
Study Completion (Actual)
November 1, 2018
Study Registration Dates
First Submitted
December 19, 2019
First Submitted That Met QC Criteria
January 21, 2020
First Posted (Actual)
January 27, 2020
Study Record Updates
Last Update Posted (Actual)
January 27, 2020
Last Update Submitted That Met QC Criteria
January 21, 2020
Last Verified
December 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- 17806 (OTHER: University of Western Ontario)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
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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