Rice to the rescue: new study tests Low-GI, High-Protein rice for diabetes prevention
NCT ID NCT07663123
First seen Jun 27, 2026 · Last updated Sep 16, 2026 · Updated 2 times
Summary
The HARVEST study is testing whether eating a special low-glycemic, high-protein rice instead of regular white rice can improve blood sugar control in people with prediabetes or type 2 diabetes. Over 16 weeks, 225 adults in Singapore will replace their usual rice with one of three types: regular white rice, low-GI rice, or low-GI high-protein rice. The goal is to see if this simple swap can lower HbA1c levels and help prevent diabetes.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- functional rice varieties (low glycemic index and high protein rice)
- What this could lead to
- If successful, this could provide a simple, culturally acceptable way to help manage blood sugar and prevent progression to type 2 diabetes without major diet changes.
- What could go wrong
- This is a relatively small, early-stage trial (225 participants) and results may not apply to other populations. The rice is a dietary supplement, not a drug, so effects may be modest.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 225 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Apr 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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40 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Males or females, aged 40 to 65 years old 2. Chinese, Malay or Indian 3. Body Mass Index between 23.0 - 32.0 kg/m2 4. Prediabetes profile as per fasting plasma glucose (≤ 6.9 mmol/L) and HbA1c level (5.7% - 6.4%) 5. Habitually consuming about 3 to 5 servings of polished white rice per day 6. No known food allergies and intolerance to food provided as part of study procedures 7. Proficient in English language 8. Willing to comply to study procedures and provide written consent Exclusion Criteria: 1. Diagnosed with Type 1 or 2 diabetes mellitus/ OGTT failure during screening visit 2. History or current diagnosis of cardiovascular, endocrine, gastrointestinal, haematological, hepatitis (hepatitis B and C), cancers (except basal cell carcinoma), chronic kidney disease or other medical conditions which may affect study outcomes, as assessed by study team 3. Having chronic medication (eg: metformin, oral corticosteroids etc), and/or supplements that may influence glycaemic management and other study outcomes, as assessed by study team 4. History of bariatric surgery 5. Significant weight change (± 5 % body weight) during the last 3 months 6. Women who are pregnant, breastfeeding or planning pregnancy 7. Drug abuse within the last 5 years 8. Excessive alcohol consumption \> 2 servings per day 9. Smoking in the last 1 year 10. Following any special diet(s) which may interfere with study outcomes (eg: Ketogenic diet, intermittent fasting, calorie-deficit) 11. Major change in physical activity and/or dietary habits in the last 3 months 12. Use of oral antibiotics in the last 3 months 13. Participation in other intervention studies, which may affect study outcomes as assessed by study team 14. Staff of IHDP and SIFBI in A\*STAR
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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