Food is Medicine in Survivorship: Pediatric Cancer Survivors and Families

This study, called FoodiiS, is looking at how a food delivery and cooking program can help families of children who have survived cancer. Researchers want to see if the program, which includes videos, recipes, and healthy eating content, is easy to use and helpful. Some families will receive the FoodiiS program with culinary ingredients, others will only receive culinary ingredients, and a control group will get the program later. The main goal is to check the safety of the program. You can join if you are a parent or guardian of a school-aged child (5-12 years old) who completed cancer treatment within the last five years, have internet access, and can speak and read English. The study plans to enroll 21 families.

Study design
This is an interventional study with three groups: FoodiiS plus Culinary Essentials Food Delivery, Culinary Essentials Food Delivery Only, and a Waitlist control group. It aims to enroll 21 participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Safety and Adverse Events (AEs) will be measured through study completion, which is an average of 1 year.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07218328

Food is Medicine in Survivorship: Examining the Feasibility and Impact of a Scalable Food Delivery and Culinary Medicine Program (FoodiiS) Among Pediatric Cancer Survivors and Their Families

Not Yet Recruiting
NAAll AgesInterventional
M.D. Anderson Cancer Center
~21 participants
Updated 2026-07-17 on ClinicalTrials.gov
What's tested:FoodiiS plus Culinary Essentials Food DeliveryCulinary Essentials Food Delivery OnlyWaitlist control

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Safety and Adverse Events (AEs)
Measured over Through study completion; an average of 1 year
Pediatric Cancer
1 sites across 1 states
Texas1
  • Marget Raber, DRPH · PRINCIPAL_INVESTIGATOR · M.D. Anderson Cancer Center

Opens a ready-to-send draft in your own email app — review before sending.

Do you actually qualify for this trial?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

Parents/guardians of school-aged (5-12 years) pediatric cancer survivors.
Have children that are within five years of having completed active treatment.
Self-report having internet access.
Self-report as being able to speak and read English.
Willing to complete study assessments.

Exclusion

Parents of pediatric cancer survivors over 12 years of age.
Unwilling or unable to complete study assessments.
Self-report to not speak English.
  • Safety and Adverse Events (AEs)Through study completion; an average of 1 year

    Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0