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
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- M.D. Anderson Cancer Center
- Enrollment
- 80
- Locations
- 2
- Primary Endpoint
- Safety and Adverse Events (AEs)
Study Overview
Brief Summary
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.
Detailed Description
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.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Single Group
- Primary Purpose
- Supportive Care
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
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
Arms & Interventions
Usual Care Waitlist Control
Participants will be assessed for study eligibility and randomized to study
Intervention: Digital culinary medicine intervention (Dietary Supplement)
Intervention Group
Participants will be assessed for study eligibility and randomized to study
Intervention: Digital culinary medicine intervention (Dietary Supplement)
Outcomes
Primary Outcomes
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
Secondary Outcomes
No secondary outcomes reported