Pediatric Cancer
Conditions
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.
Detailed description
Primary Objective: Assess the feasibility and acceptability of the FoodiiS intervention for parents of pediatric cancer survivors (recruitment, retention, satisfaction). Secondary Objective: Explore the preliminary efficacy of FoodiiS to improve diet quality and cooking behaviors among parents of pediatric cancer survivor.
Interventions
DIETARY_SUPPLEMENTFoodiiS plus Culinary Essentials Food Delivery
The FoodiiS intervention will include videos, recipes, and other online healthy eating content adapted from previously developed materials.
DIETARY_SUPPLEMENTCulinary Essentials Food Delivery Only
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.
DIETARY_SUPPLEMENTWaitlist control
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.
Sponsors
M.D. Anderson Cancer Center
Study design
Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE
Eligibility
Sex/Gender
ALL
Healthy volunteers
Yes
Inclusion criteria
* 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 criteria
* Parents of pediatric cancer survivors over 12 years of age. * Unwilling or unable to complete study assessments. * Self-report to not speak English.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| 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 |
Countries
United States
Contacts
CONTACTMargaret Raber, DRPH
PRINCIPAL_INVESTIGATORMarget Raber, DRPH
M.D. Anderson Cancer Center
Outcome results
None listed