Smartphone app aims to simplify insulin dosing for type 1 diabetes
NCT ID NCT07234500
First seen Jun 27, 2026 · Last updated Aug 12, 2026 · Updated 2 times
Summary
This study tests whether a mobile app can help people with type 1 diabetes adjust their insulin doses better than standard care. About 50 participants over age 15 will use the app or receive usual care for 3 months. The main goal is to see if the app improves blood sugar control, measured by HbA1c levels.
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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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50 people
The number who actually took part.
- Started
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Sep 2025
- Finished
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Jul 2026
- 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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15 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Patients (≥15 years), with uncontrolled (HbA1c ≥ 7) type 1 diabetes who were treated with multiple daily insulin injections (MDI) for at least 3 months before the study date. 2. Patients who are willing to test their blood glucose level at least 3 times daily during the study period. 3. Participants who will give their informed consent to participate in the study. - Exclusion Criteria: 1. Pregnant woman or planning to be pregnant 2. Patients at high risk of developing hypoglycemia (e.g., those with IHD, osteoporosis, hypoglycemia unawareness). 3. Patients with psychiatric disorders. 4. Patients who will be subjected to a major change in insulin dose (more than 20%) at the start or during the study period. 5. Patients who don't use the application during the study period. The usage Metrics of the application will be watched on Google Analytics
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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.
Contacts and locations
Locations
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Faiha Specialized Diabetes, Endocrine and Metabolism Center at Al-Faiha Teaching hospital
Basra, Basrah, Iraq