- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05309395
Food Prescriptions to Promote Affordable Diets (FoodRx)
Food Prescriptions to Promote Affordable Diets That Meet RDAs Among Multi-generational Latino Households
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
FoodRx will test the effects of a culturally sensitive meal planning and affordable grocery delivery service in a randomized controlled trial to improve diet quality, weight control and chronic disease risk among multi-generational Latino households. This will be the first study to test the effectiveness of food prescriptions and home delivery on BMI and diet quality among Latino families. Food prescriptions will meet the EAT-Lancet sustainability guidelines and achieve at least 90% of the recommended dietary allowances (RDAs) for 23 critical nutrients for all family members at a cost not exceeding $680/month, the current CalFresh [California's Supplemental Nutrition Assistance Program (SNAP)] budget allocated for a family of four. Investigators will include tailored directions on portion size based on age, sex, activity level and weight goals. Investigators will develop and validate our menus and test logistics with focus groups of Latino adults with overweight or obesity [Body mass index (BMI) >25 kg/m2]. Thereafter, 180 Latino households of 3-5 people (n=720) from Kaiser Permanente members with at least two individuals with overweight or obese and at least 1 child aged 5-10 years will participate in a 6-month randomized trial with a wait-list cross-over design. Based on the weekly menu plan, a grocery list will be generated, and items delivered to the home. Anthropometric measurements, blood pressure, and dietary intake and blood samples will be collected at baseline, 6, and 12 months. Each family will be expected to pay for the majority of grocery costs, with the amount above this covered as an incentive for participation. Specific aims are: 1. To develop an affordable and culturally sensitive meal-planning and grocery delivery intervention for Latino households. 2) To determine the impact of food prescriptions and grocery delivery on parental health and diet quality. 3) To determine the impact of food prescriptions and grocery delivery on child health and diet quality. In a cross-center aim, data from this Project will be combined with Projects 1 and 2 to examine 1) the multi-level determinants of chronic disease risk in Latino children and 2) the effects of different types of interventions and how social and environmental factors in Latino affect the response to intervention.
Measure include BMI for adults and BMI z-score (primary outcome) for children, dietary quality, cognitive function in children, blood pressure, HbA1C, blood lipids and liver function (ALT/AST) (secondary outcomes) and compare intervention with wait-list control participants. If the approach proves effective, food prescriptions could provide a scalable and sustainable model to improve the diet, health, and well-being of Latino families.
Study Type
Enrollment (Estimated)
Phase
- Phase 3
Contacts and Locations
Study Contact
- Name: Deborah A Cohen, MD, MPH
- Phone Number: 3107953960
- Email: deborah.a.cohen@kp.org
Study Contact Backup
- Name: Galina Inzhakova
- Phone Number: 6267105792
- Email: galina.inzhakova@kp.org
Study Locations
-
-
California
-
Pasadena, California, United States, 91101
- Recruiting
- Kaiser Permanente
-
Contact:
- Erika Estrada, MPH
- Email: erika.l.estrada@kp.org
-
Contact:
- Galina INzhakova, MPH
- Phone Number: 6265647752
- Email: galina.inzhkova@kp.org
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Multigenerational Latino household that has at least 2 adults with a BMI >27 kg/m2 and who both want to lose weight and at least one child under age 18; [Multi-generational is defined as having household members in two or three age groups: a) less than 18 years; b) 18-64 years; c) 65 years or older]; The household should have between 3-5 residents.
- Owns at least 1 smart phone, tablet or computer or has internet access;
- No dietary exclusions or medical conditions (e.g. chronic kidney disease, or using insulin (those with type 2 diabetes mellitus without needing insulin can participate)
- Plans to stay in the area for 12 months;
- Must not be using medications that interfere with weight loss (e.g., steroids, certain anti-depressants, anti-seizure medications),
- Willing to pay for groceries
- If on Calfresh, must be willing to pick up groceries at the store.
Exclusion Criteria:
- Chronic kidney disease,
- insulin dependent diabetes,
- dietary exclusions that are inconsistent with menus
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Food Rx- meal plans and groceries
These households will receive grocery delivery weekly for 6 months
|
Participants will receive weekly meal plans and recipes and the groceries required to prepare the recommended meals
Other Names:
|
|
Active Comparator: Wait-listed control
These households will not receive grocery delivery for the first 6 months, but will get them the second six months after recruitment.
|
Participants will receive weekly meal plans and recipes and the groceries required to prepare the recommended meals
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Weight loss
Time Frame: through study completion, an average of 1 year
|
Changes in BMI
|
through study completion, an average of 1 year
|
|
Changes in dietary quality
Time Frame: through study completion, an average of 1 year
|
Participants will complete the ASA24-2020
|
through study completion, an average of 1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in HbA1C
Time Frame: 6 months
|
biomarker of blood glucose
|
6 months
|
|
Change in SGOT/PT
Time Frame: 6 months
|
Liver function tests
|
6 months
|
|
Change in Cholesterol
Time Frame: 6 months
|
level of cholesterol
|
6 months
|
|
Change in Systolic and diastolic blood pressure
Time Frame: 6 months
|
Blood pressure
|
6 months
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Deborah A Cohen, MD,MPH, Kaiser Permanente
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- FoodRx
- P50MD017344 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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