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Behavioural Intervention

Dietary Intervention for Prediabetes

N/A
Waitlist Available
Research Sponsored by Stanford University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be 18 years of age or older
Be older than 18 years old
Must not have
Have malabsorptive disorders like celiac sprue or similar
Use of weight loss medications or specific diets
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 10 days
Awards & highlights
No Placebo-Only Group

Summary

This trial aims to identify how differences in food/exercise affect the metabolic health of people with prediabetes and T2D. It could improve personalized nutrition, allowing more targeted interventions.

Who is the study for?
This trial is for generally healthy adults over 18 living near Stanford who have prediabetes or type 2 diabetes managed by diet or metformin. Participants must not be pregnant, have cognitive impairments, malabsorptive disorders, major organ diseases, a history of bariatric surgery, heavy alcohol use, recent significant weight change, or be on certain medications.
What is being tested?
The study aims to understand how different foods and exercises affect blood sugar control in people with prediabetes and type 2 diabetes. It will involve dietary interventions to see if personalized nutrition can help manage these conditions.
What are the potential side effects?
Since this trial involves dietary interventions rather than medication or invasive procedures, side effects may include changes in digestion or food sensitivities based on the new diet regimen.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am 18 years old or older.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I have a condition that affects how my body absorbs nutrients, like celiac disease.
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I am currently using weight loss medications or following a specific diet.
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I have had weight loss surgery in the past.
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I am able to understand and follow the study's requirements.
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I do not have any major organ diseases.
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I am taking diabetes medication other than metformin.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~10 days
This trial's timeline: 3 weeks for screening, Varies for treatment, and 10 days for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Changes in postprandial metabolites response as measured by micro-sampling
Comparison of blood glucose levels after the different dietary and exercise mitigators
Secondary study objectives
Changes in personal metabolic states through the day as measured in micro-sampling by Olink proteomics
Changes in personal metabolic states through the day as measured in micro-sampling by targeted and untargeted metabolomics (LC-MS)
Changes in postprandial proteomic responses as measured in micro-sampling by Olink

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: mitigatorExperimental Treatment1 Intervention
Test different foods to see their mitigating effect on blood sugars after a rice meal.

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Who is running the clinical trial?

Stanford UniversityLead Sponsor
2,468 Previous Clinical Trials
17,496,212 Total Patients Enrolled
Yue Wu, PhDStudy DirectorStanford University
~44 spots leftby Sep 2025
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