Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT06695104

YMCA Produce Prescription Project (YPRx)

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.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

YMCA of Metropolitan Washington

Washington D.C., District of Columbia, 20009, United States

Location contact

Kristy McCarron, MPH

CONTACT

[email protected]

2158704053

Tessa Mork

CONTACT

About this study

This study is a randomized control trial testing the impact of adding disease-specific, evidence-based health education (DPP) to produce prescriptions (YPRx) on participants' health. DPP is a 12-month diabetes prevention behavioral weight loss program developed by the Centers for Disease Control and Prevention and implemented nationwide. In this study, investigators will test whether the addition of health education, coaching, and peer support through DPP improves the effectiveness of YPRx. This trial will take place in the Washington D.C. Metropolitan Area in collaboration with the YMCA of Metropolitan Washington, a provider of DPP and YPRx, Hungry Harvest, a purveyor of produce deliveries, and Amerigroup/Elevance Health, a Medicaid managed care organization. Participants will be randomized 1:1 to either participate in YPRx only or to participate in YPRx plus the DPP. The length of the trial will be 12 months for each participant, and outcomes will be measured at baseline, 4 weeks, 3 months, 6 months, 9 months, and 12 months.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Over the age of 18
  • Recipient of Medicaid through Amerigroup
  • Has never been diagnosed with type I or type II diabetes
  • Access to laptop, computer, or phone with internet, or willing to use a provided device
  • District of Columbia resident
  • Available to attend DPP classes at the scheduled recurring day and time
  • Not pregnant

Exclusion criteria

  • Under the age of 18
  • Not a recipient of Medicaid through Amerigroup
  • Has been diagnosed with type I or type II diabetes
  • No access to laptop, computer, or phone with internet
  • Not a resident of the District of Columbia
  • Cannot attend DPP classes at the scheduled recurring day and time
  • Pregnant

Treatment and study plan

YMCA Produce Rx (YPRx) Program Only (Control)

Behavioral

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.

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

Behavioral

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.

Primary outcomes

  1. Change in body weight

    Time frame: Baseline, 3 months, 6, months, 9 months, and 12 months

    Change in body weight will be measured by change in absolute pounds and percent of body weight. Participants will provide self-reported weight in pounds via quarterly online surveys at baseline, 3 months, 6 months, 9 months, and 12 months (endline).

Secondary outcomes

  1. Change in physical activity

    Time frame: Baseline, 3 months, 6, months, 9 months, and 12 months

    Change in physical activity will be measured by the change in absolute minutes of physical activity and percent change in time spent being physically active. Minutes spent being physically active over the past 7 days, self-reported via quarterly online surveys at baseline, 3 months, 6 months, 9 months, and 12 months (endline).

  2. Change in food security status

    Time frame: Baseline and 12 months

    Change in food insecurity will be measured using the 6-question U.S. Household Food Security Screener Module which ask participants about food security within the household framed around personal and familial food consumption based on the ability to afford food in the past 30 days. Responses will be self-reported via online surveys at baseline and endline (12 months).

  3. Change in participant dietary intake

    Time frame: Baseline and 12 months

    Change in dietary intake will be measured using the National Cancer Institute's Dietary Screener Questionnaire. Frequency of food and beverage consumption over the previous month will be self-reported by participants via online surveys at baseline and endline (12 months). Foods and beverages include: "Pure Fruit Juices", "Fruit", "Green Leafy or Lettuce Salad", "Fried Potatoes", "Other Kinds of Potatoes", "Cooked Beans", "Vegetables", "Salsa", "Pizza", and "Tomato Sauce". Responses to all questions will be measured using 11-point scale ranging from "Never" to "6 or more times per day" for "Pure Fruit Juices", a 9-point scale ranging from "Never" to "2 or more times per day" for all other food categories, plus an additional response option "Don't know/Prefer not to answer" for each question.

  4. Change in participant food behaviors

    Time frame: Baseline and 12 months

    Change in food behavior will be measured as the change in number of days (0-7) the participant, or someone else in their family, cooked dinner at home during the preceding week. Frequencies will be self-reported by participants via online surveys at baseline and endline (12 months).

  5. Change in personal health self-rated health assessment

    Time frame: Baseline and 12 months

    Change in self-rated health assessment will be measured by the change in participant's self-rated health assessment collected via online survey at baseline and 12 months using a five-point Likert scale ("Poor" to "Excellent") .

  6. Change in participant healthcare utilization- self-reported

    Time frame: Baseline and 12 months

    Change in healthcare utilization will be measured by the change in frequency of accessing healthcare during the three months preceding baseline and endline. This outcome will be measured by whether or not the participant accessed various types of medical attention ("Yes", "No" "Don't know/Prefer not to answer"), and if so, how many times ("None" to "16 or more" plus "Don't know/Prefer not to answer") as self-reported via online surveys at baseline and endline (12 months).

Other outcomes

  1. Change in participant healthcare utilization- healthcare records

    Time frame: Baseline and 12 months

    Change in healthcare utilization will be measured by comparing healthcare claims data at baseline and endline (12 months).

  2. Change in participant HbA1c

    Time frame: Baseline and 12 months

    Change in participant HbA1c will be measured by the absolute change and percent change in HbA1c levels retrieved from healthcare claims data at baseline and endline (12 months).

  3. YMCA Produce Rx (YPRx) program satisfaction- quantitative process measure

    Time frame: 4 weeks, 3 months, 6 months, 9 months, 12 months

    Participant satisfaction with the YMCA Produce Rx program will be self-reported via online surveys at 4 weeks, 3 months, 6 months, 9 months, 12 months. Questions will include rating: the experience measured on a 6-point Likert scale ("Very negative" to "Very positive" plus "Don't know/Prefer not to answer"), the quality of produce measured on a 5-point Likert scale ("Very high quality" to "Very low quality"), familiarity with the produce measured on a 4-point Likert scale ("Very familiar, I received produce I already purchased and ate often" to "Very new, I received produce that was unfamiliar or new to me"), the quantity of produce measured on a 3-point Likert scale ("Not enough, I ran out and would have liked to have more" to "Too much, I often had leftover produce that I didn't use").

  4. YMCA Produce Rx (YPRx) program satisfaction- qualitative process measure

    Time frame: 4 weeks, 3 months, 6 months, 9 months, 12 months

    Participant satisfaction with the YMCA Produce Rx program will be self-reported via online surveys. One question asks about difficulties or challenges with the program and is presented at 4 weeks, 3 months, 6 months, 9 months, and 12 months (endline). A second question asks if there is anything else the participant would like to share and is presented at 12 months only. Both questions will be measured using written responses submitted in open text boxes.

  5. Self-perceived YMCA Produce Rx (YPRx) program impact- quantitative measure

    Time frame: 12 months

    Self-perceived impact of the YMCA Produce Rx program on participants will be self-reported via an online survey at endline (12 months). Four questions ask participants about the program's impact on their excitement toward learning about healthy eating, ability to eat healthier, and ability to save time and money, using a 5-point Likert scale from "Strongly Disagree" to "Strongly Agree".

Study contacts

Contact information is provided by the study sponsor or research team.

Kristy McCarron, MPH

CONTACT

[email protected]

215-870-4053

Tessa Mork

CONTACT

[email protected]

2403837408

Sponsors and collaborators

Lead sponsor

Tessa Mork

Other

Collaborators

  • AmeriGroup
  • Elevance Health
  • Hungry Harvest
  • Johns Hopkins Bloomberg School of Public Health

Registry information

Acronym: YPRx

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Nov 19, 2024
Registry last updated
Nov 19, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.