Can an app and cash rewards tame type 1 diabetes in young adults?
NCT ID NCT04646473
First seen Aug 13, 2026 · Last updated Aug 14, 2026 · Updated 1 time
Summary
This trial tests a digital health program designed to help young adults with type 1 diabetes improve their blood sugar control. Participants use the SweetGoals app to set and track behavioral goals, and some also receive financial incentives for meeting those goals or access to web health coaching. The study aims to see if these digital tools can lead to better HbA1c levels over a year.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A digital health intervention combining the SweetGoals app, financial incentives, and web health coaching
- What this could lead to
- If effective, this digital approach could offer a scalable way to help young adults with type 1 diabetes better manage their blood sugar levels.
- What could go wrong
- The trial is early and results may not show a significant improvement. Success depends on participants consistently using the app and engaging with coaching.
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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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300 people
The number who actually took part.
- Started
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Jul 2021
- Finished
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Apr 2025
- 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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19 to 29 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: * Have a diagnosis of T1D for \>18 months * Have A1c ≥7.5% * Report a visit with physician managing type 1 diabetes (T1D) within the previous 6 months * Participants must use a glucometer or continuous glucose monitor compatible with Glooko. Exclusion Criteria: * Pregnancy or breast feeding * Severe medical illness that would preclude participation (e.g., cystic fibrosis, developmental disability, severe cognitive impairment) * Psychiatric illness that would preclude participation * Diabetes diagnoses other than T1D (Type 2 Diabetes, Maturity Onset Diabetes of the Young/MODY) * Use of any medications known to impact glycemic control (oral or injectable corticosteroids, beta-blockers, antipsychotic medications such as risperidone). * A history of known hemoglobinopathy, anemia, or transfusion (which could alter the validity of HbA1c measurement) * Already being engaged in a psychological intervention targeting diabetes adherence.
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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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Dartmouth College
Hanover, New Hampshire, 03755, United States
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