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RHWP Prescription Produce Plan

Richmond Health and Wellness Program (RHWP) Prescription Produce Plan (PPP) Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04995237
Acronym
PPP
Enrollment
32
Registered
2021-08-06
Start date
2021-08-05
Completion date
2021-12-16
Last updated
2023-05-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Quality of Life

Brief summary

The purpose of this research study is to find out if access to fresh produce along with individual goal setting and education influences vegetable consumption, self-management \[self-efficacy\], resilience, or quality of life. Researcher think access to fresh produce along with individual goal setting and education, may improve all of the above. This study will allow them to learn more about it.

Detailed description

This research study focused on examining how a Prescription Produce Plan (PPP) may influence vegetable consumption, self-management \[self-efficacy\], resilience, and quality of life in older adults. This research study involves meeting with a team of VCU students and faculty to learn information about nutrition. In this study, participants will be asked to do the following things: 1. Complete a total of five (5) surveys and the consent process during the enrollment visit lasting approximately 30 to 60 minutes. 2. Record their blood pressure readings and blood glucose readings \[if they already do this\] once a week in a notebook provided by the research team and then self-report the blood pressure and blood glucose readings at the next two (2) study visits. 3. Receive individualized teaching supporting obtaining the goals at this visit and future study visits. The study team will discuss with participants the contents of the produce bags and how to cook the contents of the bag. They will also work with participants to set goals for themselves. Goals for this study will focus on vegetable consumption, weight management, and either blood pressure and/or blood glucose measurements. The initial study visit may last approximately 30 minutes. 4. At the end of the initial study visit, you will receive a voucher from the Shalom Farms Mobile Market for once a week redemption over the course of 6 weeks while participating in the program. VCU Health Hub 25th Street participants will receive a produce bag at the end of this visit and will need to come to the Health Hub weekly to pick up the produce bag. 5. Subsequent study visits will focus on participant goals. Participants will meet with the study team to discuss if goals were met or not met and the study team will provide individualized teaching to support meeting participant's set goals. The study team will ask participants to meet with them twice after the initial study visit for approximately 20 to 30 minutes at each visit. These meetings will be at Week #3 and at Week #6. 6. Participants will record in provided notebooks their blood pressure, weight, and blood glucose \[if they are already checking their blood glucose prior to participating in this study\]. These measurements will also be reported during study visits. 7. Participants are asked to meet with a member of the research team after six (6) weeks of participating in the study to complete a total of three (3) post-study surveys. This visit will last approximately 30 minutes. Participation in this study will last up to 8 weeks for a total of approximately 3 hours of in person visits. Approximately 30 individuals will participate in this study.

Interventions

BEHAVIORALPPP

Participants will be provided with a weekly bag of produce, information about how to cook the produce, assistance in setting quality of life goals, and individualized teaching to support meeting participant's set goals.

Sponsors

Virginia Commonwealth University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Richmond Health Wellness Program \[RHWP\]Participant or interested in joining RHWP * age 40 and older * live in Richmond * have a desire to set goals having access to fresh produce

Exclusion criteria

• not interested in joining Richmond Health and Wellness Program

Design outcomes

Primary

MeasureTime frameDescription
Change in number of vegetable servings consumedBaseline to 6 weeksAt each study visit, participants will self report average number of vegetable servings consumed daily.
Number of participants who met blood glucose levels goals6 weeksFor participants who already monitor their blood glucose, at each study visit, participants will self report whether or not they met their glucose level goals which they set during the previous study visits
Number of participants who met blood pressure reduction goals6 weeksAt each study visit, participants will self report whether or not they met their blood pressure reduction goal which they set during the previous study visits.
Number of participants who feel healthier6 weeksAt each study visit, participants will be asked if they feel healthier (yes or no).
Number of participants who met weight management goals6 weeksAt each study visit, participants will self report whether or not they met their weight management goal which they set during the previous study visits.

Secondary

MeasureTime frameDescription
Change in self-reported blood glucose readingBaseline to 6 weeksFor participants who already monitor their blood glucose, participants will self-report the results of their blood glucose reading during the study visits.
Change in self-reported blood pressure readingBaseline to 6 weeksParticipants will be provided with an automatic blood pressure machine, shown how to use it with, and given a handout with instructions on how to record and monitor their blood pressure at home. Participant will self-report the results of their blood pressure reading during the study visits.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026