NCT07218328

Brief Summary

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

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
21

participants targeted

Target at below P25 for not_applicable

Timeline
39mo left

Started Apr 2026

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress1%
Apr 2026Jul 2029

First Submitted

Initial submission to the registry

October 16, 2025

Completed
4 days until next milestone

First Posted

Study publicly available on registry

October 20, 2025

Completed
6 months until next milestone

Study Start

First participant enrolled

April 30, 2026

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2027

Expected
2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2029

Last Updated

October 20, 2025

Status Verified

October 1, 2025

Enrollment Period

1.2 years

First QC Date

October 16, 2025

Last Update Submit

October 16, 2025

Conditions

Pediatric Cancer

Outcome Measures

Primary Outcomes (1)

  • Safety and Adverse Events (AEs)

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

    Through study completion; an average of 1 year

Study Arms (3)

Waitlist Control (No Treatment until after T1 and then Access to all FoodiiS Materials)

EXPERIMENTAL

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.

Dietary Supplement: FoodiiS plus Culinary Essentials Food DeliveryDietary Supplement: Waitlist control

FoodiiS (Digital Culnary Medicine Intervention + Culinary Essentials Food Delivery)

EXPERIMENTAL

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.

Dietary Supplement: Culinary Essentials Food Delivery Only

Culinary Essential Food Delivery Alone (No Other Intervention)

EXPERIMENTAL

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.

Dietary Supplement: Waitlist control

Interventions

FoodiiS plus Culinary Essentials Food DeliveryDIETARY_SUPPLEMENT

The FoodiiS intervention will include videos, recipes, and other online healthy eating content adapted from previously developed materials.

Waitlist Control (No Treatment until after T1 and then Access to all FoodiiS Materials)
Culinary Essentials Food Delivery OnlyDIETARY_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.

FoodiiS (Digital Culnary Medicine Intervention + Culinary Essentials Food Delivery)
Waitlist controlDIETARY_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.

Culinary Essential Food Delivery Alone (No Other Intervention)Waitlist Control (No Treatment until after T1 and then Access to all FoodiiS Materials)

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • Parents of pediatric cancer survivors over 12 years of age.
  • Unwilling or unable to complete study assessments.
  • Self-report to not speak English.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The University of Texas M. D. Anderson Cancer Center

Houston, Texas, 77030, United States

Location

Related Links

MeSH Terms

Conditions

Neoplasms

Study Officials

  • Marget Raber, DRPH

    M.D. Anderson Cancer Center

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Margaret Raber, DRPH

CONTACT

713-792-9861mpraber@mdanderson.org

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 16, 2025

First Posted

October 20, 2025

Study Start

April 30, 2026

Primary Completion (Estimated)

July 1, 2027

Study Completion (Estimated)

July 1, 2029

Last Updated

October 20, 2025

Record last verified: 2025-10

Locations

US(1)