- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05941403
Developing and Testing a Produce Prescription Implementation Blueprint to Improve Food Security in a Clinical Setting
Developing and Testing a Produce Prescription Implementation Blueprint to Improve Food Security in a Clinical Setting: A Pilot Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Healthcare providers/staff and patients will be recruited from allied Integra health centers. Following enrollment in the already existing produce prescription program ("VeggieRx"), participants will be asked if they would be interested in participating in the research study that entails surveys regarding the program. The investigators expect to recruit participants into the study starting shortly after patients get enrolled in the program. Potential participants will be informed that their decision about whether to participate in the research study will not affect their eligibility or enrollment in the VeggieRx program. They will also be informed that this study seeks to understand strategies to improve the current VeggieRx program. A research assistant will follow-up with interested patients/providers/staff and complete enrollment, consents, and a baseline assessment, either in the waiting room to complete on their own, over the phone or Zoom, OR if they choose to complete it on their own, the study team will send them the link to the consent and survey. It should be noted that participants can either choose to complete the surveys on their own through a survey link (which will be the default) or the surveys can be administered by the study staff. The study team hopes to collect baseline measures before the delivery of their first vegetables which typically begins the second week in July. While providers/staff will not be receiving vegetables, the study team also hopes to collect their baseline data when the program begins (by second week of July). Follow-up data collection for patients will occur after their final delivery (usually end of November) and provider/staff survey will also occur around that time. The study team will communicate with the program to find out when the last deliveries are occurring (not gathering any patient information, just overall timeline).
Baseline and final measures for participating patients are each expected to take approximately 15-20 minutes. In addition, VeggieRx participants will also complete a biweekly measure of engagement which will take approximately 2-minutes each time and will be sent via text message or email depending on participants' preferences throughout the duration of the 6-month VeggieRx delivery period. These questions will ask if they received their vegetable delivery, how much they liked the vegetables, how much they used them and if they fit with their families' eating habits.
As described above, providers and staff will be contacted via email/text/phone by the research assistant asking them to participate. They can complete measures with a research assistant or on their own. Baseline and follow-up surveys for providers/staff are each expected to take 10-20 min. All previously mentioned study procedures can take place in Spanish for patients whose primary language is Spanish by the research assistant research staff that is fluent in Spanish.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Rhode Island
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Providence, Rhode Island, United States, 02912
- Brown Research on Implementation and Dissemination to Guide Evidence use (BRIDGE) Program
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Providence, Rhode Island, United States, 02912
- Department of Behavioral and Social Sciences/School of Public Health
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Healthcare providers/staff Inclusion Criteria:
- 18 years of age or older
- healthcare provider/staff member who makes referrals to produce prescriptions (VeggieRx)
- fluent in English and/or Spanish
Healthcare providers/staff Exclusion Criteria
- under age 18
- have not been involved in referral process for produce prescriptions (VeggieRx)
- are not fluent in English and/or Spanish
Patient Inclusion Criteria:
- 18 years of age or older
- enrolled in the produce prescription program (VeggieRx)
- fluent in English and/or Spanish
Patient Exclusion Criteria:
- under age 18
- declined to enroll in the produce prescription program (VeggieRx)
- are not fluent in English and/or Spanish
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Enhanced Produce Prescription Implementation
The study team will develop an enhanced implementation blueprint to support uptake of the produce prescription (VeggieRx) intervention that is informed by advisory board input and includes multiple implementation strategies to address identified barriers to implementation.
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Practices make modifications to their usual produce prescription program based on an implementation blueprint.
While the exact implementation strategies to be added will be defined based on qualitative data (data collection in progress), possible implementation strategies may include training or technical assistance.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Patient Engagement with the Produce Prescription Program Questionnaire
Time Frame: Baseline
|
Patient engagement will be measured with a 4-question biweekly questionnaire that includes items rated on a 5-point (1-5) Likert-scale related to whether patients received the produce and whether they used it and liked it.
Higher scores on each item indicate higher engagement.
Scores range from 4-20.
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Baseline
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Patient Engagement with the Produce Prescription Program Questionnaire
Time Frame: Week 2
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Patient engagement will be measured with a 4-question biweekly questionnaire that includes items rated on a 5-point (1-5) Likert-scale related to whether patients received the produce and whether they used it and liked it.
Higher scores indicate higher engagement.
Scores range from 4-20.
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Week 2
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Patient Engagement with the Produce Prescription Program Questionnaire
Time Frame: Week 4
|
Patient engagement will be measured with a 4-question biweekly questionnaire that includes items rated on a 5-point (1-5) Likert-scale related to whether patients received the produce and whether they used it and liked it.
Higher scores indicate higher engagement.
Scores range from 4-20.
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Week 4
|
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Patient Engagement with the Produce Prescription Program Questionnaire
Time Frame: Week 6
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Patient engagement will be measured with a 4-question biweekly questionnaire that includes items rated on a 5-point (1-5) Likert-scale related to whether patients received the produce and whether they used it and liked it.
Higher scores indicate higher engagement.
Scores range from 4-20.
|
Week 6
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Patient Engagement with the Produce Prescription Program Questionnaire
Time Frame: Week 8
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Patient engagement will be measured with a 4-question biweekly questionnaire that includes items rated on a 5-point (1-5) Likert-scale related to whether patients received the produce and whether they used it and liked it.
Higher scores indicate higher engagement.
Scores range from 4-20.
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Week 8
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Patient Engagement with the Produce Prescription Program Questionnaire
Time Frame: Week 10
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Patient engagement will be measured with a 4-question biweekly questionnaire that includes items rated on a 5-point (1-5) Likert-scale related to whether patients received the produce and whether they used it and liked it.
Higher scores indicate higher engagement.
Scores range from 4-20.
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Week 10
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Patient Engagement with the Produce Prescription Program Questionnaire
Time Frame: Week 12
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Patient engagement will be measured with a 4-question biweekly questionnaire that includes items rated on a 5-point (1-5) Likert-scale related to whether patients received the produce and whether they used it and liked it.
Higher scores indicate higher engagement.
Scores range from 4-20.
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Week 12
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Patient Engagement with the Produce Prescription Program Questionnaire
Time Frame: Week 14
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Patient engagement will be measured with a 4-question biweekly questionnaire that includes items rated on a 5-point (1-5) Likert-scale related to whether patients received the produce and whether they used it and liked it.
Higher scores indicate higher engagement.
Scores range from 4-20.
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Week 14
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Patient Engagement with the Produce Prescription Program Questionnaire
Time Frame: Week 16
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Patient engagement will be measured with a 4-question biweekly questionnaire that includes items rated on a 5-point (1-5) Likert-scale related to whether patients received the produce and whether they used it and liked it.
Higher scores indicate higher engagement.
Scores range from 4-20.
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Week 16
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Patient Engagement with the Produce Prescription Program Questionnaire
Time Frame: Week 18
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Patient engagement will be measured with a 4-question biweekly questionnaire that includes items rated on a 5-point (1-5) Likert-scale related to whether patients received the produce and whether they used it and liked it.
Higher scores indicate higher engagement.
Scores range from 4-20.
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Week 18
|
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Patient Engagement with the Produce Prescription Program Questionnaire
Time Frame: Week 20
|
Patient engagement will be measured with a 4-question biweekly questionnaire that includes items rated on a 5-point (1-5) Likert-scale related to whether patients received the produce and whether they used it and liked it.
Higher scores indicate higher engagement.
Scores range from 4-20.
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Week 20
|
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Patient Engagement with the Produce Prescription Program Questionnaire
Time Frame: Week 22
|
Patient engagement will be measured with a 4-question biweekly questionnaire that includes items rated on a 5-point (1-5) Likert-scale related to whether patients received the produce and whether they used it and liked it.
Higher scores indicate higher engagement.
Scores range from 4-20.
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Week 22
|
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Patient Engagement with the Produce Prescription Program Questionnaire
Time Frame: Week 24
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Patient engagement will be measured with a 4-question biweekly questionnaire that includes items rated on a 5-point (1-5) Likert-scale related to whether patients received the produce and whether they used it and liked it.
Higher scores indicate higher engagement.
Scores range from 4-20.
|
Week 24
|
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Patient Engagement with the Produce Prescription Program Questionnaire
Time Frame: Week 26
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Patient engagement will be measured with a 4-question biweekly questionnaire that includes items rated on a 5-point (1-5) Likert-scale related to whether patients received the produce and whether they used it and liked it.
Higher scores indicate higher engagement.
Scores range from 4-20.
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Week 26
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Patient Engagement with the Produce Prescription Program Questionnaire
Time Frame: Week 28
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Patient engagement will be measured with a 4-question biweekly questionnaire that includes items rated on a 5-point (1-5) Likert-scale related to whether patients received the produce and whether they used it and liked it.
Higher scores indicate higher engagement.
Scores range from 4-20.
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Week 28
|
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Acceptability of Intervention Measure
Time Frame: Baseline
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Acceptability of produce prescriptions will be assessed using the 4-item Acceptability of Intervention measure with scores ranging from 1 (completely disagree) to 5 (completely agree).
Higher scores indicate higher acceptability of the intervention.
Scores range from 4-20.
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Baseline
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Acceptability of Intervention Measure
Time Frame: 6 month follow up
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Acceptability of produce prescriptions will be assessed using the 4-item Acceptability of Intervention measure with scores ranging from 1 (completely disagree) to 5 (completely agree).
Higher scores indicate higher acceptability of the intervention.
Scores range from 4-20.
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6 month follow up
|
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Feasibility of Intervention Measure
Time Frame: Baseline
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Feasibility of produce prescriptions will be assessed using the 4-item Feasibility of Intervention Measure with scores ranging from 1 (completely disagree) to 5 (completely agree).
Higher scores indicate higher feasibility of the intervention.
Scores range from 4-20.
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Baseline
|
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Feasibility of Intervention Measure
Time Frame: 6 month follow up
|
Feasibility of produce prescriptions will be assessed using the 4-item Feasibility of Intervention Measure with scores ranging from 1 (completely disagree) to 5 (completely agree).
Higher scores indicate higher feasibility of the intervention.
Scores range from 4-20.
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6 month follow up
|
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Intervention Appropriateness Measure
Time Frame: Baseline
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Appropriateness of produce prescriptions will be assessed using the 4-item Intervention Appropriateness Measure with scores ranging from 1 (completely disagree) to 5 (completely agree).
Higher scores indicate higher appropriateness of the intervention.
Scores range from 4-20.
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Baseline
|
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Intervention Appropriateness Measure
Time Frame: 6 month follow up
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Appropriateness of produce prescriptions will be assessed using the 4-item Intervention Appropriateness Measure with scores ranging from 1 (completely disagree) to 5 (completely agree).
Higher scores indicate higher appropriateness of the intervention.
Scores range from 4-20.
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6 month follow up
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Evidence-Based Practice Attitudes Scale
Time Frame: 6-month follow up
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The Evidence-Based Practice Attitudes Scale measures providers' attitudes toward evidence-based practices - specifically produce prescription programs.
Scores range from 0 (not at all) to 4 (to a very great extent); higher scores indicate more positive attitudes toward evidence-based practices.
Scores are calculated as an average and range from 0-4.
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6-month follow up
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Feasibility of Participant Enrollment
Time Frame: Baseline
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Proportion of participants who agree to enroll in the study out of those who are enrolled in the produce prescription program
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Baseline
|
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Implementation Climate Scale
Time Frame: 6 month follow up
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This measure of implementation climate will assess the innovation-specific organizational climate for implementing produce prescription programs.
Responses will be rated on a 4-point scale ranging from 0 (not at all) to 4 (very great extent).
Higher responses indicate a stronger implementation climate.
Scores are calculated as an average and range from 0-4.
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6 month follow up
|
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Implementation Readiness: Organizational Readiness for Implementing Change
Time Frame: Baseline
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This measure will assess organizations' readiness to implement a new intervention.
Responses will be rated on a 5 point scale ranging from 1 (disagree) to 5 (agree).
Higher scores indicate higher organizational readiness for change.
Scores range from 12-60.
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Baseline
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Implementation Readiness: Organizational Readiness for Implementing Change
Time Frame: 6-month follow up
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This measure will assess organizations' readiness to implement a new intervention.
Responses will be rated on a 5 point scale ranging from 1 (disagree) to 5 (agree).
Higher scores indicate higher organizational readiness for change.
Scores range from 12-60.
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6-month follow up
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Adoption of Produce Prescriptions
Time Frame: Baseline
|
Number of patients who enroll in the produce prescription program
|
Baseline
|
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Adoption of Produce Prescriptions
Time Frame: 6 month follow up
|
Number of patients who enroll in the produce prescription program
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6 month follow up
|
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Effectiveness: Food Security
Time Frame: Baseline; 6 month follow up
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Measured by the 6-item United States Department of Agriculture measure.
Total scores range from 0-6, with lower scores indicating food security.
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Baseline; 6 month follow up
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Effectiveness: Food Security
Time Frame: Baseline
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Measured by the 6-item United States Department of Agriculture measure.
Total scores range from 0-6, with lower scores indicating more food security.
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Baseline
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Effectiveness: Nutrition security
Time Frame: 6 month follow up
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measured by the 4-item Nutrition Security measure.
Responses range from "never" (0) to "always" (4).
Items are scored by finding a mean of included items.
Lower scores indicate more nutrition security.
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6 month follow up
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Effectiveness: Patient Health Questionnaire-2
Time Frame: baseline, 6-month follow up
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The 2-item Patient Health Questionnaire will be used to screen for depression.
Responses range from 0 (not at all) to 3 (nearly every day).
Scores greater than 3 suggest that major depressive disorder is likely.
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baseline, 6-month follow up
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Effectiveness: Patient Health Questionnaire-2
Time Frame: 6-month follow up
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The 2-item Patient Health Questionnaire will be used to screen for depression.
Responses range from 0 (not at all) to 3 (nearly every day).
Scores greater than 3 suggest that major depressive disorder is likely.
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6-month follow up
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Effectiveness: Dietary Screener Guide
Time Frame: baseline, 6-month follow up
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Fruit and vegetable intake will be measured by the 10-item Dietary Screener Guide, in which participants will be asked to rate the frequency with which they have eaten a variety of foods.
Responses range from "never" to "6 or more times per day."
The measure is scored using a scoring algorithm that converts survey responses to estimates of average daily dietary intake for fruits and/or vegetables.
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baseline, 6-month follow up
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Effectiveness: Dietary Screener Guide
Time Frame: 6-month follow up
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Fruit and vegetable intake will be measured by the 10-item Dietary Screener Guide, in which participants will be asked to rate the frequency with which they have eaten a variety of foods.
Responses range from "never" to "6 or more times per day."
The measure is scored using a scoring algorithm that converts survey responses to estimates of average daily dietary intake for fruits and/or vegetables.
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6-month follow up
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Hannah E Frank, PhD, Brown University
- Principal Investigator: Alison Tovar, PhD, Brown University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Other Study ID Numbers
- STUDY00000018
- 008225 (Other Grant/Funding Number: Peter G. Peterson Foundation)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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