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NCT Number: NCT06760754

Examining the Feasibility and Impact of a Clinic-based Food Farmacy and Digital Culinary Medicine Program Among Cancer Survivors Treated in a Safety Net Hospital

The goal of this study is to develop and test the feasibility of a theory-driven digital culinary medicine program among food insecure cancer survivors referred from the University of Texas MD Anderson Cancer Center Oncology Clinic at LBJ to the LBJ Food Farmacy program.

Recruiting

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The University of Texas M. D. Anderson Cancer Center

Houston, Texas, 77030, United States

Location status: Recruiting

Location contact

Margaret Raber, DRPH

PRINCIPAL_INVESTIGATOR

Maria Vazquez

CONTACT

[email protected]

713-792-7124

About this study

Primary Objective:

Determine the feasibility of study recruitment goal, intervention adherence rate, attrition rate, data completion rate, and program satisfaction rate.

Secondary Objective:

Assess the preliminary efficacy of the digital culinary medicine intervention to improve diet quality, food security, quality of life, and downstream biological indicators of cardiometabolic health from baseline to post-intervention, as well as from baseline to 6 month follow up, among food insecure cancer survivors.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Cancer survivors treated at the MD Anderson Oncology Program at LBJ Hospital over 18 years of age.
  • Screen positive for food insecurity using the 2 question clinic-screener (Hunger Vital Signs)
  • Receive referral to the LBJ Food Farmacy.
  • Are within the first 5 years off of acute cancer treatment.
  • Self-report having internet access.
  • Self-report as being able to speak and read English or Spanish.
  • Willing to complete study assessments.

Exclusion criteria

  • Unwilling or unable to complete study assessments
  • Anyone under 18 years of age
  • Self-report to not speak or read English or Spanish

Treatment and study plan

Digital culinary medicine intervention

Dietary Supplement

Participants will receive 30lbs of healthy foods through an on-site hospital-base food pantry

Primary outcomes

  1. Safety and Adverse Events (AEs)

    Time frame: 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

Study contacts

Contact information is provided by the study sponsor or research team.

Maria Vazquez

CONTACT

[email protected]

713-792-7124

Sponsors and collaborators

Lead sponsor

M.D. Anderson Cancer Center

Other

Registry information

Important dates

Study start
2025
Primary completion
2028
Study completion
2028
First posted
Jan 7, 2025
Registry last updated
Feb 19, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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