Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at UCSF
Dates
study started
completion around
Principal Investigator
by Alexis Beatty, MD (ucsf)
Headshot of Alexis Beatty
Alexis Beatty

Description

Summary

The purpose of this research is to see if offering more navigation and text-message support will help increase participation and engagement in a Food is Medicine program. The study will recruit people currently participating in cardiac rehabilitation. People will be randomly assigned to 1 of 4 study groups: navigation, text-messaging, both, or neither. People will complete surveys at the start of the study and after 3 months. After 3 months, we will compare how many Food is Medicine meals or groceries people in each group received.

Official Title

SUPeRFOOD: Enhanced SUPport for Initiation and paRticipation in a FOOD is Medicine Program

Keywords

Cardiac Rehabilitation, Nutrition, Healthy, Nutrition Poor, food insecurity, nutrition insecurity, food is medicine, Malnutrition, Navigation, Text Messaging

Eligibility

You can join if…

Open to people ages 18 years and up

  1. Age 18 or older
  2. Participating in UCSF Cardiac Rehabilitation
  3. Able to communicate in English or Spanish
  4. Resident of San Francisco County

You CAN'T join if...

  1. Enrolled in hospice
  2. Unable to consent for self

Location

  • University of California, San Francisco accepting new patients
    San Francisco California 94143 United States

Lead Scientist at University of California Health

  • Alexis Beatty, MD (ucsf)
    Alexis Beatty, MD, MAS is a cardiologist and health services researcher who studies innovative delivery models for cardiovascular disease care to improve outcomes and reduce disparities. She received a career development award from the Department of Veterans Affairs to develop and test a mobile application to improve participation in cardiac rehabilitation, called VA FitHeart.

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
University of California, San Francisco
ID
NCT06500962
Study Type
Interventional
Participants
Expecting 84 study participants
Last Updated