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University of Wyoming (UW) and Wyoming Food for Thought Project (WFFTP) propose to collaboratively develop, pilot, and evaluate a trial on the impact of market vouchers on food security and fruit and vegetable (F&V) consumption. We will (a) provide farmers market vouchers to families who are enrolled in WIC, SNAP, or free or reduced lunch and/or have incomes ≤185% of poverty line; (b) assess impacts of these supports on household food security and F&V consumption; and (c) test feasibility and impacts of vouchers valid only for F&V vs. for any foods that can be purchased with SNAP.
To test the feasibility and preliminary impacts of this approach, we will enroll 30 individuals/households in this study, randomizing 10 to each of the 2 intervention arms and 10 to waitlist control. Qualifying individuals and families will be able to enroll in the study at the WFFTP Tuesday afternoon/evening market on July 30th, 2019. They will be randomized upon enrollment to one of three conditions: receiving $20 in vouchers at each of up to 4 markets ($80 total) that are good for F&V only, receiving $20 vouchers at each of up to 4 markets that are good for any foods that SNAP/EBT benefits can be used for; or delayed intervention/waitlist control (who, at the final data gathering, will receive 5 x $20 in vouchers good at the WFFTP 2019 and 2020 markets).
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Inclusion criteria
To be eligible for the intervention, a participant must be an adult aged ≥18 years old whose household is enrolled in or eligible for SNAP, free or reduced school lunch program, and/or WIC (i.e., incomes of ≤185% of poverty for household size). UW staff wills screen for eligibility by verifying a participant has an EBT card. If no card is available, participants will be asked to self-report household income and size and UW staff will use the Federal Poverty Level chart to determine the individual's eligibility. They must also self-identify as living in Casper, Wyoming. They must come in person to the market on July 30th, 2019, to enroll.
Exclusion criteria
Not meeting the criteria above.
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30 participants in 3 patient groups
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Data sourced from clinicaltrials.gov
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