Actively Recruiting
Assessing Dietary Patterns and Implementing Cost-effective Interventions to Encourage a Plant-based Diet in an Underserved Urban Population
Led by University of Louisville · Updated on 2024-10-01
300
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University of Louisville
Lead Sponsor
O
Oatly Group AB
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are studying dietary habits and food preferences among underserved urban populations who experience food insecurity. The study aims to encourage plant-based eating by providing education and affordable resources, focusing on patients of primary care clinics who have screened positive for food insecurity since 2021. The goal is to understand how readiness to change diet relates to food neophobia and to assess the impact of educational aids and subsidized produce access on diet adherence. Participants may receive educational materials about the benefits of a plant-based diet along with simple recipes and food swaps. Some patients can also choose to enroll in a subsidized Community Supported Agriculture (CSA) program that provides weekly farm produce boxes during the growing season. The study compares those receiving education alone with those who receive education plus access to subsidized produce. Enrollment and diet adherence are tracked before, during, and after the CSA period. Throughout the study, patients will complete surveys such as the Food Neophobia inventory and a Diet Inventory at multiple time points. Researchers will also gather qualitative feedback to understand participants' experiences. Secondary outcomes include monitoring changes in weight, blood pressure, hemoglobin A1C, and lipid profiles where applicable. Data privacy is maintained by de-identifying patient information and securely storing data. Participation lasts approximately one year with ongoing assessments during that time.
CONDITIONS
Brief Title
Encouraging a Plant Based Diet in an Underserved Urban Population
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients age 18 and older screening as food insecure since 2021
- Patients willing to complete survey data
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
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Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote) for eligibility screening and initial survey completion
Duration - Up to 1 year
Participants receive education about the benefits of a plant-based diet, and those who opt-in are provided with free or subsidized Community Supported Agriculture produce shares during the growing season.
Periodic surveys and assessments at baseline, during, and after the produce share period
Duration - Up to 1 year after intervention start
Participants complete follow-up surveys to assess dietary adherence, food neophobia, and health measures such as weight, blood pressure, and lipid profile.
Follow-up assessments at 1 year
Trial Site Locations
Total: 1 location
1
University of Louisville Ambulatory Internal Medicine Resident Clinic
Louisville, Kentucky, United States, 40202
Actively Recruiting
Research Team
E
Erin Murphy
A
Anuja Abhyankar
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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