CClinicalTrials.gg
RecruitingNCT06940817CHEF-EDUpdated Sep 30, 2026

Cooking HEalthy and Facilitating Early Childhood Development: CHEF-ED Study

An interventional study of CHEF-ED + Food Delivery and Food Delivery Only in Teaching Healthy Cooking Skills to Parents and Their Preschool Children, sponsored by Baylor College of Medicine. Recruiting at 1 site in United States. Open to participants aged 18 Years to 64 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-30.

Sponsored by Baylor College of Medicine · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
300
Allocation
Randomized
Ages
18 Years to 64 Years
Sex
All
01

Study summary

This study aims to test a new online program we developed for parents and their preschool children, called CHEF-ED. CHEF-ED focuses on healthy cooking, parental feeding practices, and involving children in home food preparation.

Read the detailed description

All study activities take place online over a 3-month period, and participants are randomly assigned to one of three groups: the CHEF-ED + Food Delivery group, the Food Delivery Only group, or the control group. Participants will not know to which group they are assigned until after they complete the time point 1 surveys. The assignment will be determined randomly using a computer program (equivalent to flipping a coin).

To test how well the program works, regardless of group assignment, participants are asked to complete surveys at two different time points: Time point 1 = pre-program, shortly after enrollment, and Time point 2 = post-program, about 8-10 weeks later. The surveys take about 2 hours to complete online at each time point and will include questions about the participant's and their child's dietary intake, their cooking frequency/quality, food parenting practices, and program content retention. Surveys will also include questions about family's demographics (such as participant's and their child's date of birth, ethnicity, race, sex, etc.), and household food access.

The CHEF-ED + Food Delivery group receives a one-time home food delivery of healthy cooking ingredients and kitchen utensils, such as cooking oil, spices, whole wheat pasta, low sodium soy sauce, bowls, and recipe books. Participants in this group also receive links to weekly CHEF-ED online lessons via text /email message for 7 weeks. Each weekly lesson will include a short video, infographics, and recipes.

The Food Delivery Only group receives a one-time home food delivery of healthy cooking ingredients and kitchen utensils, but no other program materials.

The control group receives no program materials or food delivery.

About 8-10 weeks after completing the time point 1 surveys, participants will receive links to complete the time point 2 surveys. After completing the post-program surveys, participants who were in the Food Delivery Only or control group will receive additional program materials that were not previously provided due to their group assignment. This means that the Food Delivery Only group, after completing the time point 2 surveys, will receive links to all of the CHEF-ED program materials (videos, infographics, recipes) and, the control group, after completing the time point 2 surveys, will receive the one-time healthy ingredients and kitchen utensils delivery and links to all of the CHEF-ED program materials.

Additionally, participants in the CHEF-ED + Food Delivery group, after the post-program surveys, may be invited to take part in an interview to share their experience with the program. This interview will be conducted over the phone or a video conference platform. The information participants share during the interview, such as suggestions and insights on materials accessibility, will help us improve the program.

02

Conditions studied

  • Teaching Healthy Cooking Skills to Parents and Their Preschool Children

Browse trials for

Keywords

  • Food security
  • Nutrition education
  • Cooking practices
  • Feeding practices
  • Chronic disease
03

Who can participate

Ages eligible
18 Years to 64 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Parents/caregivers of preschooler children ages 3 to 5 living in the greater Houston area.
  • Must have access to the Internet through a smartphone, tablet, laptop, or desktop computer.
  • Should be able to read, write, and communicate in English or Spanish.

Exclusion criteria

Exclusion Criteria:

  • Parents/caregivers and children who have any kind of food allergies, medical conditions, or dietary restrictions that may affect participation in the program.
  • Parents/caregivers under the age of 18.
  • Parents/caregivers of children with severe developmental delays.
04

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
300 participants (estimated)

Study arms

  • Experimental
    CHEF-ED + Food Delivery group

    Participants in this arm will receive a one-time delivery of non-perishable basic culinary ingredients and kitchen utensils and access to the CHEF-ED program, which includes weekly online program materials, such as videos, infographics, and recipes sent via text or email over 7 weeks.

    Behavioral: CHEF-ED + Food Delivery

  • Active comparator
    Food Delivery Only group

    Participants in this arm receive a one-time delivery of non-perishable basic culinary ingredients and kitchen utensils but will not have access to the CHEF-ED program during the study period.

    Behavioral: Food Delivery Only

  • No intervention
    Control group

    Participants in this arm will not receive the healthy cooking ingredients delivery nor will they have access to the CHEF-ED program during the study period.

Interventions

  • BehavioralCHEF-ED + Food Delivery

    CHEF-ED is a 7-week, digital, video-based parental intervention that teaches healthy cooking practices and an optimal way to involve children in home cooking. Each week features a video, infographics, and recipe content. The content is designed to be integrated into the home food environment without major changes to shopping habits. However, some basic culinary ingredients that are featured may not already be part of participating family pantry stocks. To support participants in effectively learning the healthy cooking strategies, participating families are provided a one-time home food delivery of non-perishable basic culinary ingredients and kitchen utensils, such as cooking oil, spices, whole wheat pasta, low sodium soy sauce, bowls.

  • BehavioralFood Delivery Only

    The Food Delivery Only intervention involves participants receiving a one-time home food delivery of non-perishable basic culinary ingredients and kitchen utensils, such as cooking oil, spices, whole wheat pasta, low sodium soy sauce, bowls.

05

What researchers measure

Primary outcomes

  1. Child diet quality

    Parent report of child dietary intake using a validated food frequency survey.

    Time frame: From baseline assessment to the post-intervention assessment. The intervention program is 7 weeks.

Secondary outcomes

  1. Parent diet quality

    Self-report of diet quality using a validated diet history questionnaire.

    Time frame: From baseline assessment to the post-intervention assessment. The intervention program is 7 weeks.

  2. Parent cooking frequency/quality

    Self-report of healthy cooking using a validated questionnaire.

    Time frame: From baseline assessment to the post-intervention assessment. The intervention program is 7 weeks.

  3. Food parenting practices

    Second order constructs from a validated food parenting questionnaire - encourage trying new foods; structure; external control.

    Time frame: From baseline assessment to the post-intervention assessment. The intervention program is 7 weeks.

  4. Knowledge of best feeding practices

    Six items related to child eating behaviors reported by parents.

    Time frame: From baseline assessment to the post-intervention assessment. The intervention program is 7 weeks.

Other outcomes

  1. Sample characteristics

    Self-report of demographic information, food security status, and acculturation.

    Time frame: From baseline assessment to the post-intervention assessment. The intervention program is 7 weeks.

06

Study locations

1 of 1 sites recruiting
  • Baylor College of Medicine
    Houston, Texas 77030, United States
    • Arely Y. Balderas, BA · Contact · arely.balderas@bcm.edu · 713-798-9175
    • Nilda Micheli, BS · Contact · nildam@bcm.edu · 713-798-6737
    • Sheryl O. Hughes, PhD · Principal investigator
    Recruiting
07

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT06940817
Lead sponsor
Baylor College of Medicine
Collaborators
M.D. Anderson Cancer Center
Responsible party
Sheryl Hughes (Professor, Baylor College of Medicine) — Principal investigator
First posted
Apr 23, 2025
Start date
Jun 19, 2025
Primary completion
Aug 31, 2027 (estimated)
Completion
Aug 31, 2027 (estimated)
Last update
Sep 30, 2026

Study contacts

Sheryl O. Hughes, PhD
Contact
shughes@bcm.edu
713-798-7095
Arely Y. Balderas, BA
Contact
arely.balderas@bcm.edu
713-798-9175
Sheryl O. Hughes, PhD
principal investigator · Baylor College of Medicine

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion