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Clinical Trials/NCT06661538
NCT06661538
Recruiting
Phase 2

Addressing Food Insecurity in the Health Care Setting to Promote Health Equity

University of California, San Diego2 sites in 1 country600 target enrollmentAugust 18, 2025
ConditionsFood Insecurity

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Food Insecurity
Sponsor
University of California, San Diego
Enrollment
600
Locations
2
Primary Endpoint
Feasibility of Intervention Measure (FIM)
Status
Recruiting
Last Updated
5 months ago

Overview

Brief Summary

Food insecurity (FI) disproportionately affects those who have been historically marginalized and significantly contributes to poor health outcomes. In children, FI is associated with lower psychosocial functioning and academic achievement. It also contributes to the development of adverse health outcomes such as obesity, type 2 diabetes mellitus (T2DM), cardiovascular disease (CVD), and Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD). Improving the diet quality of children (e.g., decreasing fat intake, increasing fruits and vegetables (FV) and fiber intake) has been associated with lower fasting serum glucose, insulin, LDL cholesterol, non-HDL cholesterol, and reduced risk of CVD later in life. Increasing awareness and access to programs that promote food equity by providing affordable healthy produce is a promising way to improve health outcomes and empower patients and communities to achieve better health and well-being. The goal of this proposal is to refine and optimize implementation strategies that connect families to community-based food security nutrition support programs through health care systems or medical clinics. The investigators will develop a multi-disciplinary, cross-sector collaboration to optimize current processes and workflows that integrate food security nutrition support programs into the healthcare system. The investigators will also work to develop a closed-loop communication system between the healthcare and healthy food access systems to support greater patient autonomy and self-efficacy to obtain, prepare, and consume healthy foods.

Detailed Description

The investigators will conduct a pilot type 2 hybrid effectiveness-implementation trial of the I-FRESH (Implementing Food Referrals for Equity and Sustained Health) program using a Roll-Out Implementation Optimization (ROIO) design among families with children with nutrition-related illnesses who receive Medicaid or Supplemental Nutrition Assistance Program (SNAP) benefits. The I-FRESH program, the food security nutrition support program, will be refined prior to the first clinic roll-out based on input from several hospital, clinical, and community stakeholders. The program will involve 4 main components: screening and identification of families experiencing food insecurity (FI); social worker/care navigator-led discussions with families to determine need and readiness to receive support; referrals and assistance to engage with these programs; and follow-up assessments to determine fit, track utilization, and determine need for additional referrals. With each roll-out into a new clinic, modified implementation procedures and work-flows will be evaluated using implementation and effectiveness outcomes.

Registry
clinicaltrials.gov
Start Date
August 18, 2025
End Date
March 31, 2028
Last Updated
5 months ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Kay Rhee

Professor

University of California, San Diego

Eligibility Criteria

Inclusion Criteria

  • child attending Type 1 or Type 2 Diabetes clinics, Cardiology clinic, MASLD clinic, general GI clinic at RCHSD
  • child age between 5-18 years old
  • parent or caregiver who indicates that they are experiencing food insecurity and receives Medicaid or SNAP benefits
  • family not moving out of the San Diego area within the time frame of the study
  • Limited exclusion criteria will be applied in order to examine the impact of this program on a heterogenous group of people and increase generalizability. Of note, all genders and races/ethnicities will be allowed to participate.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Feasibility of Intervention Measure (FIM)

Time Frame: 12 months

4-item measure that assesses feasibility of implementing the program in that setting; score range (4-20) with higher scores referring to greater feasibility

Acceptability of Intervention Measure (AIM)

Time Frame: 12 months

4-item measure assessing the acceptability of the program by program staff and participants; score range (4-20) with higher scores referring to greater acceptability

Implementation Fidelity

Time Frame: 12 months

Percent of families with food insecurity that were called, percent of families that were referred to a program or provided with resources, percent of families that received follow-up phone calls, percent of families that needed additional resources/referrals

Adoption

Time Frame: 12 months

Percent of clinical settings approached that participate; characteristics of settings participating compared to non participating clinical settings

Reach

Time Frame: 12 months

Percent of families attending clinic that completed the food insecurity screener, number of families experiencing food insecurity in that clinic, percent of families that wanted and did not want referrals to a nutrition support program

Secondary Outcomes

  • Change in Food Security levels over a 12 month period(12 months)
  • Change in Weight Status over 12 months(12 months)
  • Change in Blood Pressure over 12 months(12 months)
  • Change in non-fasting and fasting Lipid levels over 12 months(12 months)
  • Change in HbA1c over 12 months(12 months)
  • Change in Liver Function Tests over 12 months(12 months)
  • Change in Quality of Life measure over 12 months(12 months)

Study Sites (2)

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