Actively Recruiting
Salud Diabetes: A Pilot Study Comparing Lifestyle Interventions and Real-Time Continuous Glucose Monitoring
Led by Sutter Health · Updated on 2025-05-31
200
Participants Needed
1
Research Sites
49 weeks
Total Duration
On this page
Sponsors
S
Sutter Health
Lead Sponsor
W
William Marsh Rice University
Collaborating Sponsor
AI-Summary
What this Trial Is About
The aim of this proposal is to determine the impact of a produce prescription program in predominantly Hispanic/Latino adults with established non-insulin treated T2D and an HbA1c at or above 9%.
CONDITIONS
Official Title
Salud Diabetes: A Pilot Study Comparing Lifestyle Interventions and Real-Time Continuous Glucose Monitoring
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged over 18 years with established type 2 diabetes
- HbA1c of 9% or higher from a test within the last 6 months
- Agreement to track glucose levels only using the study-provided continuous glucose monitor (CGM)
You will not qualify if you...
- Type 1 diabetes
- Use of insulin
- Pregnancy
- Use of steroids or medications that impact glucose levels, including atypical antipsychotics (clozapine, olanzapine, paliperidone, quietiapine, risperidone), corticosteroids, calcineurin inhibitors (cyclosporine, sirolimus, tacrolimus), and protease inhibitors (atazanavir, darunavir, fosamprenavir, indinavir, nelfinavir, ritonavir, saquinavir, tipranivir)
- Life expectancy less than 6 months
- Diagnosis of stage 5 kidney disease or risk of needing dialysis as judged by the investigator
- Any active clinically significant disease or disorder that may interfere with study participation as judged by the investigator
- Inability to follow study procedures as judged by the investigator
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Sansum Clinic, Sutter Health
Santa Barbara, California, United States, 93110
Actively Recruiting
Research Team
D
David Kerr, PhD
CONTACT
B
Brett Avery
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
1
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