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Can texting and rewards get teens to take their insulin?

NCT ID NCT05280184

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether combining text message reminders with small rewards (behavioral economics) could help 173 teens with type 1 diabetes take their insulin more consistently. Participants used an insulin pump and had a history of missing mealtime doses. The goal was to improve their average blood sugar (HbA1c) and daily insulin use. The trial has completed, but some key data on time in range were not available due to vendor issues.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
behavioral economics incentives and automated text message reminders
What this could lead to
If successful, this approach could offer a low-cost, non-drug way to help teens with type 1 diabetes better manage their insulin dosing and blood sugar levels.
What could go wrong
This was a small, completed feasibility study, not a large-scale trial. The primary outcome on time in range was unavailable due to data access issues, limiting conclusions.

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

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

173 people

The number who actually took part.

Started

Jan 2023

Finished

Sep 2025

Lead sponsor

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

11 to 17 years

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * adolescents between 11.0-17.0 years old and their parent/guardian; * adolescents have a physician confirmed diagnosis of type 1 diabetes of at least 6 months duration; * adolescents use an insulin pump for daily type 1 diabetes self-management; * adolescents evidence sub-optimal daily BOLUS scores (a mean daily BOLUS score \<2.5) Exclusion Criteria: * adolescents who do not use an insulin pump; adolescents who have an allergy or sensitivity to the adhesive and/or skin preparation used for CGM; * adolescents with a comorbid chronic condition (e.g., renal disease); * adolescents and parents who do not speak English

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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

  • Children's Mercy Kansas City

    Kansas City, Missouri, 64108, United States

  • Nemours Children's Health

    Jacksonville, Florida, 32207, United States

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