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YMCA Produce Prescription Project (YPRx)

NCT06695104 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2024-11-19

No results posted yet for this study

Summary

In this randomized control study, participants will be randomized 1:1 to either participate in the YMCA's Produce Prescription Program (YPRx) and receive weekly deliveries of fresh produce bags for their household or to receive YPRx plus participate in the Diabetes Prevention Program (DPP).

The investigators hypothesize that participants randomized to receive YPRx plus DPP will have greater weight loss, increased physical activity, improved diet quality and behaviors, increased food security, improved self-rated health assessment, decreased healthcare utilization from baseline to endline (12 months) compared to those randomized to receive YPRx produce deliveries only.

We will also collect data on process measures for implementation purposes.

Conditions

  • Pre-diabetes

Interventions

BEHAVIORAL

YMCA Produce Rx (YPRx) Program Only (Control)

Participants in the control group will receive weekly, home-delivered produce bags of fresh vegetables and fruits and sized for each participants' household. Produce deliveries will be administered for 52 weeks.

BEHAVIORAL

YMCA Produce Rx (YPRx) Program + the Diabetes Prevention Program (DPP)

Participants will receive weekly, home-delivered produce bags of fresh vegetables and fruits and sized for each participants' household. Produce deliveries will be administered for 52 weeks. Additionally, participants will be registered for a free, year-long YMCA membership and enrolled in the DPP. Through the DPP, participants will receive health education, coaching, and peer support via 26 virtual group sessions over a year.

Sponsors & Collaborators

  • AmeriGroup

    collaborator UNKNOWN

  • Hungry Harvest

    collaborator UNKNOWN

  • Johns Hopkins Bloomberg School of Public Health

    collaborator OTHER

  • Elevance Health

    collaborator INDUSTRY

  • Tessa Mork

    lead OTHER

Principal Investigators

  • Kristy McCarron, MPH · YMCA of Metropolitan Washington

  • Julia Wolfson, PhD MPP · Johns Hopkins Bloomberg School of Public Health

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-01-06
Primary Completion
2026-03-30
Completion
2026-06-30

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06695104 on ClinicalTrials.gov