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Type 1 DiabetesCoin2DoseNCT05280184

Coin2Dose: Behavioral Economics to Promote Insulin BOLUS Activity and Improve HbA1c in Teens

A study testing Coin2Dose in people with Type 1 Diabetes, run by Nemours Children's Clinic at 2 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Our objective is to test the feasibility, acceptability, and initial efficacy of using behavioral economics incentives (BEI) in a novel, semi-automated intervention to target daily insulin BOLUS scores in adolescents with suboptimal insulin use. Read more about this study

Who is it for?
Ages 11 to 17 years
Conditions the study is for
Type 1 Diabetes
What is being tested?
Coin2Dose
Could I receive a placebo?
No, everyone receives an active treatment
How many people
173 participants
Where
2 sitesUnited States
Study dates
1 Jan 2023to 30 Sep 2025
Phase
Interventional
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 11 to 17 years
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • 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)

Who cannot join

  • 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

Trial locations and contacts

2 sites in 1 country.

United States2 sites
  • Nemours Children's Health

    Jacksonville, Florida, 32207

  • Children's Mercy Kansas City

    Kansas City, Missouri, 64108

Other trials in United States

About this study

Our objective is to test the feasibility, acceptability, and initial efficacy of using behavioral economics incentives (BEI) in a novel, semi-automated intervention to target daily insulin BOLUS scores in adolescents with suboptimal insulin use.

Read the detailed description

This R01 responds to PAS-20-160 (Small R01s for Clinical Trials Targeting Diseases within the Mission of NIDDK). Our objective is to test the feasibility, acceptability, and initial efficacy of using behavioral economics incentives (BEI) in a novel, semi-automated intervention to target daily insulin BOLUS scores in adolescents with suboptimal insulin use. There is a critical need for efficacious and easy to implement interventions targeting self-management behaviors in adolescents with type 1 diabetes (T1D). This is because national registry data suggest that only between 15-28% of adolescents achieve their glycated hemoglobin (HbA1c) target, thereby placing the majority of them at increased risk for serious acute and long-term complications. BEI interventions are efficacious for promoting health behaviors including frequency of self-monitoring blood glucose (SMBG) in youth. Moreover, there is evidence that BEI can be relatively easy to implement, especially when using Non-Contingent BEI. But with the uptake of integrated insulin pump and continuous glucose monitor (CGM) systems and the new FDA approval enabling youth to dose for insulin based solely on CGM, we believe the long-term value of targeting SMBG alone in BEI interventions is limited and that daily insulin use is the next logical self-management target. Building off of our prior work, the insulin BOLUS score offers a specific, measurable, and valid treatment target for daily insulin use that is also more closely related to HbA1c than SMBG or Total insulin boluses per day. Thus our Aims are: 1) examine the feasibility and acceptability of our semi-automated BEI intervention (called Coin2Dose) that targets daily BOLUS scores in adolescents and 2) examine the preliminary efficacy of Coin2Dose versus a standard care control (SC) group on youth daily BOLUS scores, HbA1c, and glucose time in range (TIR). We also include an exploratory aim to examine the incremental impact of using Contingent versus Non-Contingent BEI within our Coin2Dose intervention on youth's BOLUS scores, HbA1c, and TIR. Coin2Dose will deliver automated text messages to cue adolescents to bolus for insulin, plus BEI for daily BOLUS activity. To enhance the scientific rigor of this R01, we will use the ORBIT Model for behavioral intervention development. Consistent with this model, we will recruit 180 adolescents and a parent to participate in 1- a telehealth focus group (ORBIT Phase 1a: Define; n= 20), 2- a formative pre-test (ORBIT Phase 1b: Refine; n=10), or 3- a pilot randomized clinical trial (ORBIT Phase 2: RCT Pilot; n=150). Our RCT Pilot will randomize teens with suboptimal insulin use (BOLUS score <2.5; 70% of teens based on pilot data) to a SC or 1 of 2 versions of Coin2Dose that only differ based on our use of personalized (Contingent) v. non-personalized (Non-Contingent) BEI. Adolescents will participate in 12-weeks of active treatment, plus a 12-week follow-up period. This small R01 is Significant for its potential to yield: 1- preliminary data supporting our new BEI intervention targeting daily BOLUS scores, which may also improve youth HbA1c, 2- novel data exploring the incremental impact of Contingent v. Non-Contingent BEI, which has implications for Coin2Dose as well as the broader uptake of BEI interventions.

Conditions
Type 1 Diabetes
Being tested
Coin2Dose
Medical subject headings
Diabetes Mellitus, Type 1

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Coin2DoseBehavioural

    Behavioral Economics incentive intervention that also combines automated text message reminders to dose for insulin

Study groups in NCT05280184
Study groupRoleWhat they receive
Coin2DoseExperimentalBEI intervention that also combines automated text message reminders to dose for insulin; will test Contingent and Non-Contingent BEI
Receives: Behavioral: Coin2Dose
Standard Care ControlNo interventionStandard care control group; will not receive automated text message reminders to dose for insulin nor BEI for daily BOLUS scores

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Glycated Hemoglobin- HbA1c

    proxy measure of average glycemic levels

    Measured: change in week 0 outcome at week 13

  2. Change in Daily Insulin Bolus Score

    valid, objective measure of insulin use in youth with type 1 diabetes; range 0-3, higher scores reflect greater adherence to mealtime insulin use

    Measured: change in week 0 outcome at week 13

Secondary outcomes (1)
  1. Change in Glucose Time in Range (70-180 mg/dL)

    Change in percent time spent with glucose levels between 70-180mg/dL. Time in Range (TIR) data were unavailable for all participants due to unresolved legal/contractual barriers with external CGM vendors. Efforts to resolve these issues are ongoing, we will update with results if data access becomes possible.

    Measured: change in week 0 outcome at week 13

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Mar 2022
  2. Study start1 Jan 2023
  3. Primary completion30 Jun 2025
  4. Study completion30 Sep 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
173 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05280184
Sponsor's protocol ID
1770218
Acronym
Coin2Dose
Status last verified
Jan 2026
First submitted
15 Feb 2022
Last updated
11 Feb 2026
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: Undecided. Will not share data that may make it possible to identify individual participants.

Publications

  • Patton SR, Fox L, Cushing CC, McDonough R, Clements MA. Cash-Only INcentives to promote insulin DOSE engagement: A protocol paper for the pilot randomized controlled trial of COIN2DOSE. Contemp Clin Trials. 2022 Dec;123:107008. doi: 10.1016/j.cct.2022.107008. Epub 2022 Nov 14.

    PubMed 36396067

Questions about this trial

What is this clinical trial studying?

A study testing Coin2Dose in people with Type 1 Diabetes, run by Nemours Children's Clinic at 2 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 11 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Yes. Results are posted in the registry (first posted 11 Feb 2026). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Glycated Hemoglobin- HbA1c (time frame: change in week 0 outcome at week 13). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05280184, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Feb 2026.

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