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

Primary Purpose

Type 1 Diabetes

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Coin2Dose
Sponsored by
Nemours Children's Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 1 Diabetes

Eligibility Criteria

11 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Nemours Children's HealthRecruiting
  • Children's Mercy Kansas CityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Coin2Dose

Standard Care Control

Arm Description

BEI intervention that also combines automated text message reminders to dose for insulin; will test Contingent and Non-Contingent BEI

Standard care control group; will not receive automated text message reminders to dose for insulin nor BEI for daily BOLUS scores

Outcomes

Primary Outcome Measures

Change in Glycated Hemoglobin- HbA1c
proxy measure of average glycemic levels
Change in Glucose time in range
another proxy measure of average glycemic levels
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

Secondary Outcome Measures

Full Information

First Posted
February 15, 2022
Last Updated
February 28, 2023
Sponsor
Nemours Children's Clinic
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1. Study Identification

Unique Protocol Identification Number
NCT05280184
Brief Title
Coin2Dose: Behavioral Economics to Promote Insulin BOLUS Activity and Improve HbA1c in Teens
Acronym
Coin2Dose
Official Title
Coin2Dose: Behavioral Economics to Promote Insulin BOLUS Activity and Improve HbA1c in Teens
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 1, 2023 (Actual)
Primary Completion Date
March 31, 2024 (Anticipated)
Study Completion Date
April 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Nemours Children's Clinic

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief 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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 1 Diabetes

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Coin2Dose
Arm Type
Experimental
Arm Description
BEI intervention that also combines automated text message reminders to dose for insulin; will test Contingent and Non-Contingent BEI
Arm Title
Standard Care Control
Arm Type
No Intervention
Arm Description
Standard care control group; will not receive automated text message reminders to dose for insulin nor BEI for daily BOLUS scores
Intervention Type
Behavioral
Intervention Name(s)
Coin2Dose
Intervention Description
Behavioral Economics incentive intervention that also combines automated text message reminders to dose for insulin
Primary Outcome Measure Information:
Title
Change in Glycated Hemoglobin- HbA1c
Description
proxy measure of average glycemic levels
Time Frame
change in week 0 outcome at week 13
Title
Change in Glucose time in range
Description
another proxy measure of average glycemic levels
Time Frame
change in week 0 outcome at week 13
Title
Change in daily insulin Bolus score
Description
valid, objective measure of insulin use in youth with type 1 diabetes; range 0-3, higher scores reflect greater adherence to mealtime insulin use
Time Frame
change in week 0 outcome at week 13

10. Eligibility

Sex
All
Minimum Age & Unit of Time
11 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Susana R Patton, PhD
Phone
9046972000
Email
susana.patton@nemours.org
First Name & Middle Initial & Last Name or Official Title & Degree
Kristen Morga
Email
kristen.morga@nemours.org
Facility Information:
Facility Name
Nemours Children's Health
City
Jacksonville
State/Province
Florida
ZIP/Postal Code
32207
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Susana R Patton, PhD
Phone
913-697-3595
Email
sp0105@nemours.org
Facility Name
Children's Mercy Kansas City
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64108
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mark Clements, MD PHD
Phone
816-234-3000
Email
endoclinicaltrials@cmh.edu

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
Undecided. Will not share data that may make it possible to identify individual participants.

Learn more about this trial

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

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