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Sweetgoals for Type 1 Diabetes

Primary Purpose

Type 1 Diabetes

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
SweetGoals app
Coaching
Incentives
Sponsored by
Trustees of Dartmouth College
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Type 1 Diabetes

Eligibility Criteria

19 Years - 29 Years (Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • Dartmouth CollegeRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

App only

App plus Incentives

App plus Coaching

App plus Coaching plus Incentives

Arm Description

Sweetgoals app only

SweetGoals app + incentives=yes + coaching=no

Sweetgoals app + incentives=no + coaching=yes

Sweetgoals app + incentives=yes + coaching=yes

Outcomes

Primary Outcome Measures

HbA1c
Mean HbA1c

Secondary Outcome Measures

Glucose checking adherence
Mean proportion of days in the past 30 meeting daily glucose checking goal
Problem solving
Mean score on the Social Problem Solving Inventory-Revised

Full Information

First Posted
November 16, 2020
Last Updated
February 2, 2023
Sponsor
Trustees of Dartmouth College
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
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1. Study Identification

Unique Protocol Identification Number
NCT04646473
Brief Title
Sweetgoals for Type 1 Diabetes
Official Title
Thinking Outside the Clinic: A Digital Health Approach for Young Adults With Type 1 Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 29, 2021 (Actual)
Primary Completion Date
October 31, 2025 (Anticipated)
Study Completion Date
October 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Trustees of Dartmouth College
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

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
The study will test an app and web-delivered intervention designed to improve glycemic control (HbA1c) among young adults with Type 1 diabetes. All participants will receive the "core" digital intervention, the SweetGoals app, focused on self-monitoring and goal setting. Efficacy of two independent intervention components (incentives for adherence and web health coaching) will be tested
Detailed Description
ASSIGNMENT OF PARTICIPANTS: Interested participants will download the SweetGoals app. Once all screening procedures are complete, including A1c verification via the mail in test kit, research staff will schedule a web video meeting to (1) randomize participants and inform them of their intervention condition assignment; (2)assist participants in setting up their Glooko account and uploading their devices and orient them to the Glooko data visualization hub; and (3) download the Glooko mobile app, which may be used by all participants and into which participants without a Glooko compatible pump will enter carb counts. INTERVENTION DELIVERY: All participants will receive the core intervention, the SweetGoals app. Those assigned to Incentives will receive the app plus incentives for meeting adherence goals. Those assigned to Coaching will receive web health coaching to increase motivation and skill in self-management as described below. DIABETES CARE FOR ALL PARTICIPANTS: Participants in all conditions will receive ongoing treatment for type 1 diabetes from their current medical provider. Report of a visit within the past 6 months is a study inclusion criterion. Study staff will not provide medical care or intervention. All participants will receive information about recommendations for medical care related to diabetes (e.g., quarterly visits and A1c assessment, consistent with Standards of Medical Care in Diabetes). Informational links will be provided within SweetGoals for various online resources addressing T1D educational topics. CORE INTERVENTION FOR ALL PARTICIPANTS: SWEETGOALS APP All participants will receive the SweetGoals app, an automated intervention that sets weekly self-management goals and provides weekly feedback. The SweetGoals app will be implemented and delivered using the MobileCoach app platform, which runs on both Android and iOS systems. The SweetGoals app sends weekly reminders to upload devices, retrieves device data via the Glooko API, applies decision rules to evaluate daily and weekly goals, and sends weekly feedback messages about goal adherence and encouragement about adherence in the upcoming week. Diabetes Self-Management Goals. Glooko stores multiple variables that are used to evaluate the glucose monitoring and mealtime goals. Across both glucose monitoring and mealtime target behaviors, we use a similar structure to the goals to promote ease of remembering the goals and communication with participants. Specifically, regardless of the devices used or the target (glucose monitoring or mealtime behaviors) there is a daily adherence goal, and there is a weekly goal of meeting the daily goal on >5 days each week. These weekly goals were selected to promote high consistency in mealtime glucose monitoring and carb counting. Each week, participants will be asked to set personal goals for the next week for the number of days they think they can meet each daily goal. Each week they will receive a message stating the number of days on which they met each goal, how that compared to their personal goal, and whether they met the ultimate weekly goal (met daily goal >5 days per week). Glucose monitoring goals. Each participant will receive a device-specific (glucometer vs. CGM) daily goal based on the device they use to monitoring their glucose levels, and the ultimate weekly goal for all participants is to meet the daily goal on at least 5 days per week. For participants who use a glucometer only, the daily self-monitoring of blood glucose (SMBG) goal is >5 checks, each >2 hours from another check. For participants who use CGM, the CGM wear time goal is 80% of expected values each day. Expected values per day are based on the device-specific check frequency (e.g., every 5 mins for Dexcom G6). We selected this cutoff to reflect clinically necessary glucose monitoring frequency, but also allow for legitimate disconnect time (sports, leisure activities) and sensor changes. Mealtime goals. Each participant will receive daily goals specific to their insulin delivery method (pump vs. MDI). Participants will be asked to check their glucose before they eat (if they use a glucometer only, not CGM). Participants who use a Glooko compatible pump will only need to use their pump to document the mealtime goals. If they use a pump+glucometer combination that requires manual entry of the glucose value into the pump, they must complete the glucose check and that manual entry no longer than 30 minutes before the carb entry to receive credit for meeting the mealtime goal. If they use a pump+CGM or other meter that transfers the glucose value to the pump without manual entry, no manual entry is necessary. If they use MDI (no insulin pump), they will use the Food event screen to enter their carb counts in the Glooko smartphone app. When each participant's Glooko data are retrieved, our algorithm evaluates whether or not there is a valid glucose value within 30 minutes prior to each carb entry. The daily mealtime target is 3 paired glucose level/carb count values. INCENTIVE COMPONENT In addition to using the SweetGoals app, participants assigned to Incentives will also receive incentives for meeting goals. Incentives to improve adherence to glucose monitoring and mealtime behaviors that support appropriate insulin bolusing are paid weekly from weeks 1-11, then fade in frequency from weeks 12-25, a procedure used to promote long lasting improvements in adherence and A1c. In the fading phase, incentives are paid at increasing time intervals (i.e., 2,3,4 then 5-week delays; paid at weeks 13, 16, 20, 25). For meeting daily and weekly goals, participants can earn the following incentives: (1) $1 for each day meeting glucose monitoring goal. (maximum=$7 per week); (2) $5 per week bonus for meeting the glucose monitoring goal 6 or 7 days to promote consistent weekly glucose monitoring. (maximum=$5 per week) (3) $1 for every day with >3 properly timed glucose value/carb entry pairs (maximum=$7 per week); (4) $5 per week bonus for meeting the mealtime goal 6 or 7 days to promote consistent weekly glucose checking and carb counting at mealtime. (maximum=$5 per week). Total earnings possible each week are $24 (~$3.50 per day). The maximum earnings for all goals are $600 across 25 weeks. Research staff will load earned incentives on reloadable prepaid MasterCards. WEB HEALTH COACHING COMPONENT: Participants assigned to coaching will also receive 15 Web Health Coaching sessions by a bachelors-level health coach. These coaching sessions are designed to promote effective self-management of diabetes. Coaching sessions are held weekly from weeks 1-11, then fade over the second half of the intervention with 4 sessions held during weeks 12-25 (weeks 13, 16, 20, and 25). Sessions 1-7 are 30 minutes each, as new material is introduced and practiced. Sessions 8-15 are 15 minutes each, as problem solving skills are practiced and applied to new challenges identified by participants. Coaching will be completed using Zoom, an online HIPAA compliant web conference system.

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
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
App only
Arm Type
Experimental
Arm Description
Sweetgoals app only
Arm Title
App plus Incentives
Arm Type
Experimental
Arm Description
SweetGoals app + incentives=yes + coaching=no
Arm Title
App plus Coaching
Arm Type
Experimental
Arm Description
Sweetgoals app + incentives=no + coaching=yes
Arm Title
App plus Coaching plus Incentives
Arm Type
Experimental
Arm Description
Sweetgoals app + incentives=yes + coaching=yes
Intervention Type
Behavioral
Intervention Name(s)
SweetGoals app
Intervention Description
App offers goal setting and feedback
Intervention Type
Behavioral
Intervention Name(s)
Coaching
Intervention Description
Web health coaching
Intervention Type
Behavioral
Intervention Name(s)
Incentives
Intervention Description
Financial incentives for meeting goals
Primary Outcome Measure Information:
Title
HbA1c
Description
Mean HbA1c
Time Frame
+12 months
Secondary Outcome Measure Information:
Title
Glucose checking adherence
Description
Mean proportion of days in the past 30 meeting daily glucose checking goal
Time Frame
+12 months
Title
Problem solving
Description
Mean score on the Social Problem Solving Inventory-Revised
Time Frame
+12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
29 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Catherine Stanger, Ph.D.
Phone
603-646-7023
Email
catherine.stanger@dartmouth.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Catherine Stanger, Ph.D.
Organizational Affiliation
Trustees of Dartmouth College
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dartmouth College
City
Hanover
State/Province
New Hampshire
ZIP/Postal Code
03755
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Catherine Stanger, Ph.D.
Phone
603-646-5109
Email
catherine.stanger@dartmouth.edu

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Data will be made available to other researchers and practitioners, while safeguarding the privacy of participants and protecting confidential and proprietary data and third-party intellectual property. Findings will be published as soon as they are available in relevant peer-reviewed journals that are available online, and share as requested directly to the author(s). Data requests can be made directly to the Principal Investigator with information for accessing the data on the NIDDK Data Repository.
IPD Sharing Time Frame
If the study ends and data are no longer being obtained directly from study participants by study investigators, all study data will be provided to the Repository by the end of the funding period (which may include no-cost extensions). The period of exclusive use of the entire dataset from the study will be for three years after the last study contact for collection of intervention outcomes.
IPD Sharing Access Criteria
Data requests made directly to the Principal Investigator or through the NIDDK Data Repository
Citations:
PubMed Identifier
33620330
Citation
Stanger C, Kowatsch T, Xie H, Nahum-Shani I, Lim-Liberty F, Anderson M, Santhanam P, Kaden S, Rosenberg B. A Digital Health Intervention (SweetGoals) for Young Adults With Type 1 Diabetes: Protocol for a Factorial Randomized Trial. JMIR Res Protoc. 2021 Feb 23;10(2):e27109. doi: 10.2196/27109.
Results Reference
derived

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Sweetgoals for Type 1 Diabetes

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