Could a phone app learn to count carbs and dose insulin?
NCT ID NCT07884526
First seen Oct 20, 2026 · Last updated Oct 21, 2026 · Updated 1 time
Summary
Researchers are testing a mobile app called AI-CARE that uses artificial intelligence to estimate carbohydrates from photos of meals and suggest mealtime insulin doses. The study enrolls adults with type 1 or type 2 diabetes who take multiple daily insulin injections and wear a continuous glucose monitor. Participants are randomly assigned to use the app or receive usual care for 12 weeks. The trial measures whether the app is practical to use, whether it is safe, and how it affects blood sugar and quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- an AI-powered mobile app that estimates carbohydrates from meal photos and suggests insulin doses
- What this could lead to
- If it works, the app could help people with diabetes adjust mealtime insulin more easily and keep blood sugar in a safer range.
- What could go wrong
- This is a small, short pilot study, so it can only show whether the app is practical and safe enough to test further. The AI may misjudge carb amounts, and insulin dosing errors can cause dangerous low blood sugar.
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 48 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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Oct 2028
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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21 years and older
- 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: * have type 1 or type 2 diabetes and are receiving multiple daily insulin injections * have an HbA1c ≥7% * are willing to wear a CGM sensor for 12 weeks * are able to read and understand English. Exclusion Criteria: * are pregnant * have experienced severe hypoglycaemia or diabetic ketoacidosis within the preceding three months * have hypoglycaemia unawareness * insulin-to-carbohydrate ratio is below 8 * have significant cognitive impairment that may interfere with the use of the application.
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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 places running it
1 site. The list below names each one and where it is.
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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.
Contacts and locations
Locations
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Tan Tock Seng Hospital
Singapore, Singapore, 308433, Singapore
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Effectiveness and safety of the RIGHTEST™ continuous glucose monitoring system for blood glucose management in persons with diabetes mellitus
- A model for delivering strength training and nutrition education for older adults (MoveStrong): a pilot randomized controlled trial
- A phase III, randomized, Open-Label, Active-Controlled study to evaluate the efficacy and safety of enicepatide versus tirzepatide among participants with type 2 diabetes and inadequate glycemic control on oral Glucose-Lowering medications
- Agreement of the estimated 1-Repetition-Maximum between two Multiple-Repetition-Maximum tests with different weight in patients with cardiovascular disease or risk factors
- Effectiveness of a structured nutrition educational program on glycemic control, quality of life, and cardiovascular risk in patients with uncontrolled diabetes using multiple daily insulin injections