NCT07011251Completed
Food Insecurity, Food as Medicine, Hypertension
Development of a User Centered Design Approach for Screening, Referral, and Enrollment in Food as Medicine Among Adults
Source: ClinicalTrials.gov · Last updated 1 Apr 2026
Brief summary (registry, in English)
Development of a user centered design to understand how a tailored food is medicine program based on user preferences and needs improves engagement and clinical outcomes. The study will examine how patients, screened either face to face or through automated for food insecurity, engage in a food is medicine program over 12-weeks.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 159 (actual)
- First submitted
- 30 May 2025
- Start date
- 16 Aug 2024
- Primary completion date
- 29 Jan 2025
- Lead sponsor
- Alison Gustafson
- Diseases
- High blood pressure
- NCT number
- NCT07011251
What you commit to
- Study type: Interventional
- Participants enrolled: 159
- From 16 Aug 2024 to the primary completion date, 29 Jan 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Considering bariatric surgery in the next year or prior bariatric surgery
- Known drug or alcohol misuse in the past 2 years
Other
- Participant in weight research intervention in last 12 months
- Lack of safe, stable residence and ability to store meals
- Lack of telephone which can receive text messages
- Pregnancy/breastfeeding or intended pregnancy in the next year
Who the study is looking for
- Diagnosis of Hypertension in last 12 months
- Experiencing food insecurity as indicated by 2-item Hunger Vital Sign
- English or Spanish speaking
- No plans to move from the area for at least 1 year
- Willing and able to accept text messages
- Free living to the extent that participant has control over dietary intake
- Willing and able to provide written informed consent and participate in all study activities.
Age in the registry: 18 years to 64 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Appalachian Regional Healthcare Coordinator of this site? Confirm its status | Floyd | United States | Unknown status |
Related publications
This page is information, not medical advice. Discuss any trial with your doctor.