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

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FoodiiS plus Culinary Essentials Food Delivery — DIETARY_SUPPLEMENT
The FoodiiS intervention will include videos, recipes, and other online healthy eating content adapted from previously developed materials.
Culinary Essentials Food Delivery Only — DIETARY_SUPPLEMENT
To support participants in effectively learning the healthy cooking strategies and mitigate access issues, investigators will provide participating families two home food deliveries of non-perishable culinary ingredients that are related to HCI practices including whole grain versions of common products (brown rice, whole wheat flour), healthier cooking oils (olive and canola), and a core selection of herbs and spices, among other goods.
Waitlist control — DIETARY_SUPPLEMENT
The control group will receive no intervention until after T1. After the T1 data collection time point, the control group will receive all FoodiiS intervention materials.

The goal of this research study is to learn if the FoodiiS-Kids intervention is useful to parents and guardians of pediatric cancer survivors.

Experimental: Waitlist Control (No Treatment until after T1 and then Access to all FoodiiS Materials)
Target participants for this study will be parents/guardians of school-aged (5-12 years) pediatric cancer survivors that are within first 5 years off active treatment.
Experimental: FoodiiS (Digital Culnary Medicine Intervention + Culinary Essentials Food Delivery)
Target participants for this study will be parents/guardians of school-aged (5-12 years) pediatric cancer survivors that are within first 5 years off active treatment.
Experimental: Culinary Essential Food Delivery Alone (No Other Intervention)
Target participants for this study will be parents/guardians of school-aged (5-12 years) pediatric cancer survivors that are within first 5 years off active treatment.

Safety and Adverse Events (AEs) [ Time Frame: Through study completion; an average of 1 year ]

Facility	City	State	ZIP	Site coordinators
The University of Texas M. D. Anderson Cancer Center	Houston	Texas	77030	Margaret Raber, DRPH [email protected]

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