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
NCT ID: NCT06760754
Last Updated: 2025-07-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
80 participants
INTERVENTIONAL
2025-03-31
2028-01-01
Brief Summary
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Detailed Description
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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.
Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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Usual Care Waitlist Control
Participants will be assessed for study eligibility and randomized to study
Digital culinary medicine intervention
Participants will receive 30lbs of healthy foods through an on-site hospital-base food pantry
Intervention Group
Participants will be assessed for study eligibility and randomized to study
Digital culinary medicine intervention
Participants will receive 30lbs of healthy foods through an on-site hospital-base food pantry
Interventions
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Digital culinary medicine intervention
Participants will receive 30lbs of healthy foods through an on-site hospital-base food pantry
Eligibility Criteria
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Inclusion Criteria
* 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
* Anyone under 18 years of age
* Self-report to not speak or read English or Spanish
18 Years
ALL
No
Sponsors
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M.D. Anderson Cancer Center
OTHER
Responsible Party
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Principal Investigators
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Margaret Raber, DRPH
Role: PRINCIPAL_INVESTIGATOR
M.D. Anderson Cancer Center
Locations
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The University of Texas M. D. Anderson Cancer Center
Houston, Texas, United States
Countries
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Central Contacts
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Facility Contacts
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Related Links
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MD Anderson Cancer Center Website
Other Identifiers
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NCI-2024-10265
Identifier Type: OTHER
Identifier Source: secondary_id
2024-1732
Identifier Type: -
Identifier Source: org_study_id
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