Medically Tailored Meals for Kids with Pediatric Cancer

This study, called "Medically Tailored Meals for Kids," is testing if providing healthy, frozen meals to families of children with cancer is practical and well-received. The intervention involves delivering up to 10 medically tailored meals per week for 12 weeks, along with condiments. The study aims to enroll 30 participants, including children aged 12-17 who are receiving cancer treatment at UNC Chapel Hill and have experienced taste changes from chemotherapy. To be eligible, children must have completed at least one cycle of chemotherapy and expect to undergo at least two more. Researchers will measure success by asking parents and adolescents about their experiences with the meals at the beginning and end of the 12-week period. The study is currently unclear on its recruitment status.

Study design
This is an interventional study with a planned enrollment of 30 participants. It is not specified if it is randomized or blinded.
What's involved
Participants will receive up to 10 healthy, frozen meals per week for 12 weeks. Parents and adolescents will complete surveys at the start and end of the 12-week period.
Compensation
Not stated in the trial record.
Follow-up
Participants will be assessed at Baseline and 12 weeks.

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NCT06814795

Medically Tailored Meals for Kids

Active, Not Recruiting
NAAges 12–99InterventionalHealth services
UNC Lineberger Comprehensive Cancer Center
~32 participants
Updated 2026-08-27 on ClinicalTrials.gov
What's tested:Medically tailored meals

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Parent-reported feasibility, acceptability, appropriateness and accessibility of MTM-Kids
Measured over Baseline and 12 weeks
+1 more outcome measured
Pediatric Cancer
1 sites across 1 states
North Carolina1
  • Sheila J. Santacroce · PRINCIPAL_INVESTIGATOR · University of North Carolina, Chapel Hill

This trial hasn't published a contact. View it on ClinicalTrials.gov

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Eligibility criteria

Inclusion

be under the care of The University of North Carolina at Chapel Hill School of Medicine, Department of Pediatrics, Division of Pediatric Hematology/Oncology
have completed at least one cycle of cancer chemotherapy that included an agent known to cause alterations in taste,
expect to undergo at least two more cycles,
be aged 12-17.9 years
communicate in English or Spanish.
be the primary parental caregiver of a study-eligible child,
be aged 18 years or older
communicate in English or Spanish.
  • Parent-reported feasibility, acceptability, appropriateness and accessibility of MTM-KidsBaseline and 12 weeks

    Each domain will be measured by 4-items developed by others and adapted for this study. Parents will be asked to read each item and indicate their response using 5-point scales anchored by 1=completely disagree and 5=completely aDomain scores will be calculated by summing item responses and dividing the sum by 4. Domain score range is 1-higher scores indicating better MTM program feasibility, acceptability, appropriateness and accessibility.

  • Adolescent-reported acceptability and appropriateness of MTM-KidsBaseline and 12 weeks

    Each of these two domains of feasibility will be measured using items developed and validated by others and adapted for this study. Each domain has 4-items. Adolescents will be asked to read each item and indicate their response using scales anchored by 1=completely disagree and 5=completely agree. Domain scores will be calculated by summing responses and dividing the sum by 4. Domain score range is 1-4, with higher scores indicating better acceptability appropriateness