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Culturally Tailored Meals and Blood Sugar in Asian Americans With Type 2 Diabetes

Tests culturally tailored meals against usual diet in adults with type 2 diabetes.

Plain-language title generated from the registry record
Registry title: Using Continuous Glucose Monitoring to Quantify the Effects of NOURISH's Culturally Modified Meals on Asian Americans With Type 2 Diabetes

Key facts

Where
Stanford, United StatesSee the site

Where in United States

  • Stanford UniversityStanford, United StatesTaking people

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Trial details

Who runs it
Stanford University
Trial code
NCT06836479
Record updated
28 September 2026
Original description
The investigators are hoping to determine whether tailoring the diet of someone with type 2 diabetes to their ethnic group while following American Diabetes Association guidelines can make a significant difference in their blood sugar controls. Participants will be required to wear a Continuous Glucose Monitor (CGM) for 1-month so that the investigators can compare blood sugar levels when participants are eating their routine diet vs. the culturally tailored diabetes diet.Read full original descriptionShow less

Validation of NOURISH Project's Culturally Tailored Meals on Postprandial Glycemic Response Using Continuous Glucose Monitoring: A Quantitative and Qualitative Study

The investigators are hoping to determine whether tailoring the diet of someone with type 2 diabetes to their ethnic group while following American Diabetes Association guidelines can make a significant difference in their blood sugar controls. Participants will be required to wear a Continuous Glucose Monitor (CGM) for 1-month so that the investigators can compare blood sugar levels when participants are eating their routine diet vs. the culturally tailored diabetes diet.

Inclusion: Self-identification as Asian Indian or Filipino; Diagnosed with T2DM; Pick up and consume personally tailored cultural food and meal options for 1 week; Willing to wear a CGM for 30 days.

Exclusion: Currently taking insulin; Known severe allergic reactions and/or food intolerances that would interfere with the ability to eat; Those who, in the opinion of the investigators, cannot reliably complete the study protocol.

ClinicalTrials.gov NCT06836479