RECRUITING

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

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

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

Quick Facts

Study Start:2025-03-31
Study Completion:2028-01-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06760754

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Cancer survivors treated at the MD Anderson Oncology Program at LBJ Hospital over 18 years of age.
  2. * Screen positive for food insecurity using the 2 question clinic-screener (Hunger Vital Signs)
  3. * Receive referral to the LBJ Food Farmacy.
  4. * Are within the first 5 years off of acute cancer treatment.
  5. * Self-report having internet access.
  6. * Self-report as being able to speak and read English or Spanish.
  7. * Willing to complete study assessments.
  1. * Unwilling or unable to complete study assessments
  2. * Anyone under 18 years of age
  3. * Self-report to not speak or read English or Spanish

Contacts and Locations

Study Contact

Maria Vazquez
CONTACT
713-792-7124
mrvazquez1@mdanderson.org

Principal Investigator

Margaret Raber, DRPH
PRINCIPAL_INVESTIGATOR
M.D. Anderson Cancer Center

Study Locations (Sites)

The University of Texas M. D. Anderson Cancer Center
Houston, Texas, 77030
United States

Collaborators and Investigators

Sponsor: M.D. Anderson Cancer Center

  • Margaret Raber, DRPH, PRINCIPAL_INVESTIGATOR, M.D. Anderson Cancer Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-03-31
Study Completion Date2028-01-01

Study Record Updates

Study Start Date2025-03-31
Study Completion Date2028-01-01

Terms related to this study

Additional Relevant MeSH Terms

  • Cancer