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Research on Optimizing the Use of Technology With Education (ROUTE-T1D)

Primary Purpose

Type 1 Diabetes, Continuous Glucose Monitoring, Behavioral Intervention

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
diabetes education and parent coaching support
Sponsored by
Children's National Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 1 Diabetes

Eligibility Criteria

10 Years - 15 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 10-15 years old
  • Type 1 diabetes
  • Type 1 diabetes diagnosis ≥ 6 months \
  • Starting a continuous glucose monitor for the first time or restarting after ≥ 1 year

Exclusion Criteria:

  • Younger than 10, older than 15
  • Diagnosed less than 6 months
  • Already using CGM or has used within last year
  • Other major medical condition such as cancer, cystic fibrosis

Sites / Locations

  • Children's National Research InstituteRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Immediate intervention

Wait-list/delayed intervention

Arm Description

Participants randomized to the immediate intervention group will participate in 3 video-conferencing sessions with a Certified Diabetes Care and Education Specialist (CDCES) interventionist and connect with a peer parent consultant immediately post randomization (expected intervention duration: 3 months).

Participants randomized to the delayed intervention group will receive no intervention for 6 months post-randomization; after the 6-month follow-up period, the delayed intervention group also will participate in 3 video conferencing sessions with a CDCES interventionist and connect with a peer parent consultant (expected intervention duration: 3 months).

Outcomes

Primary Outcome Measures

Glycemic control
hemoglobin A1c (HbA1c)
Glycemic control
hemoglobin A1c (HbA1c)
Glycemic control
hemoglobin A1c (HbA1c)
Glycemic control
hemoglobin A1c (HbA1c)
glycemic variability
Using 14-30 days of CGM data
glycemic variability
Using 14-30 days of CGM data
glycemic variability
Using 14-30 days of CGM data
glycemic variability
Using 14-30 days of CGM data

Secondary Outcome Measures

Family Conflict
The Diabetes Family Conflict Scale-Revised Scored 19-57 where a higher score indicates higher family conflict
Family Conflict
The Diabetes Family Conflict Scale-Revised Scored 19-57 where a higher score indicates higher family conflict
Family Conflict
The Diabetes Family Conflict Scale-Revised Scored 19-57 where a higher score indicates higher family conflict
Family Conflict
The Diabetes Family Conflict Scale-Revised Scored 19-57 where a higher score indicates higher family conflict
Diabetes Distress
Problem Areas in Diabetes scales (PAID) Scored 14-84 where higher scores indicate higher distress
Diabetes Distress
Problem Areas in Diabetes scales (PAID) Scored 14-84 where higher scores indicate higher distress
Diabetes Distress
Problem Areas in Diabetes scales (PAID) Scored 14-84 where higher scores indicate higher distress
Diabetes Distress
Problem Areas in Diabetes scales (PAID) Scored 14-84 where higher scores indicate higher distress
CGM benefits and burdens
Continuous glucose monitoring (CGM) Burdens and Benefits as assessed by The BenCGM and BurCGM
CGM benefits and burdens
Continuous glucose monitoring (CGM) Burdens and Benefits as assessed by The BenCGM and BurCGM
CGM benefits and burdens
Continuous glucose monitoring (CGM) Burdens and Benefits as assessed by The BenCGM and BurCGM
CGM benefits and burdens
Continuous glucose monitoring (CGM) Burdens and Benefits as assessed by The BenCGM and BurCGM
CGM use
Indicators of CGM use, including mean days work per week, will be evaluated to measure sustained use of CGM.
CGM use
Indicators of CGM use, including mean days work per week, will be evaluated to measure sustained use of CGM.
CGM use
Indicators of CGM use, including mean days work per week, will be evaluated to measure sustained use of CGM.
CGM use
Indicators of CGM use, including mean days work per week, will be evaluated to measure sustained use of CGM.
Diabetes self-management
The Diabetes Management Questionnaire (DMQ)-a self- and parent-report measure assessing the frequency of engagement in diabetes care behaviors (e.g. BG monitoring, adjusting behavior to specific situations) over the past month. Scored 0-100 with higher scores indicating higher adherence to diabetes management
Diabetes self-management
The Diabetes Management Questionnaire (DMQ)-a self- and parent-report measure assessing the frequency of engagement in diabetes care behaviors (e.g. BG monitoring, adjusting behavior to specific situations) over the past month. Scored 0-100 with higher scores indicating higher adherence to diabetes management
Diabetes self-management
The Diabetes Management Questionnaire (DMQ)-a self- and parent-report measure assessing the frequency of engagement in diabetes care behaviors (e.g. BG monitoring, adjusting behavior to specific situations) over the past month. Scored 0-100 with higher scores indicating higher adherence to diabetes management
Diabetes self-management
The Diabetes Management Questionnaire (DMQ)-a self- and parent-report measure assessing the frequency of engagement in diabetes care behaviors (e.g. BG monitoring, adjusting behavior to specific situations) over the past month. Scored 0-100 with higher scores indicating higher adherence to diabetes management

Full Information

First Posted
August 26, 2022
Last Updated
September 29, 2022
Sponsor
Children's National Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT05564481
Brief Title
Research on Optimizing the Use of Technology With Education
Acronym
ROUTE-T1D
Official Title
Optimizing Technology Uptake and Use in Hard to Reach Adolescents With Type 1 Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 1, 2022 (Actual)
Primary Completion Date
July 1, 2026 (Anticipated)
Study Completion Date
December 30, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Children's National Research Institute

4. Oversight

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

5. Study Description

Brief Summary
Consistent use of continuous glucose monitors (CGM) has the potential to improve glycemic control and related type 1 diabetes (T1D) health outcomes, however young adolescents with T1D are the least likely age group to begin and sustain use of CGM. The proposed study will conduct a feasibility trial of a behavioral intervention designed to optimize use of CGM in adolescents specifically targeting underrepresented populations in diabetes technology research.
Detailed Description
Young adolescents (ages 10-15) with type 1 diabetes (T1D) are at high risk for deterioration of glycemic control and relatedly poor overall T1D self-management. Continuous glucose monitors (CGM) provide real-time indicators of glucose levels and alert users to hypoglycemia and hyperglycemia. Consistent, informed use of CGM has the potential to improve glycemic control and related T1D health outcomes. However, adolescents with T1D are the least likely age group to utilize CGM and significant health disparities exist in access to and use of CGM among youth from racial and ethnic minority backgrounds and youth with public insurance. Adolescent CGM users also continue to evidence A1c levels above recommended targets, potentially due challenges related to perceived CGM burden and related family functioning. Novel, developmentally targeted interventions delivered early in adolescence could promote optimal uptake and use of CGM and reduce psychosocial barriers to sustained use but must be evaluated in rigorous pilot trials that attend to health disparities. The current study proposes to evaluate an innovative behavioral intervention that utilizes certified diabetes care and education specialists (CDCES) to teach problem-solving and communication skills around CGM data and use, targeting adolescent-parent T1D interactions related to glucose data, individualized CGM challenges, and weekly adolescent-parent joint review of CGM reports. The intervention also addresses HCP knowledge of health disparities in diabetes technology through interactive education, and boosts family support through connection with peer parent consultants. This study aims to evaluate the preliminary efficacy of the behavioral intervention to enhance CGM use and resulting T1D health outcomes. Sixty adolescents and their parents will be recruited for this pilot randomized trial, randomly assigned to either an immediate intervention group or a delayed intervention group serving as a standard care comparison. Intervention content will be delivered via 3 telemedicine sessions with adolescents and a parent and supported by connection with a peer parent consultant. Medical and psychosocial data (including A1c, CGM indicators, CGM burdens and benefits, diabetes distress, and diabetes-related family conflict) will be collected from adolescents and a parent at baseline and three follow-up time points across the first year after CGM initiation. The investigators will employ quantitative and qualitative analyses to evaluate intervention feasibility, acceptability, and impact. Enhancing CGM access and use at this key developmental juncture provides an excellent opportunity for tailored support and problem-solving, resulting in potentially lasting improvement in diabetes self-management. Results of this pilot trial will directly inform a multi-site randomized clinical trial to evaluate efficacy, with the long term goal of identifying effective behavioral strategies that can be integrated into routine diabetes education and care.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 1 Diabetes, Continuous Glucose Monitoring, Behavioral Intervention, Parent-Child Relations

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
wait-list control; all participants receive intervention- randomized to start immediately or 6 months after CGM start
Masking
Outcomes Assessor
Masking Description
a research assistant blind to condition of participant will complete outcome assessments.
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Immediate intervention
Arm Type
Experimental
Arm Description
Participants randomized to the immediate intervention group will participate in 3 video-conferencing sessions with a Certified Diabetes Care and Education Specialist (CDCES) interventionist and connect with a peer parent consultant immediately post randomization (expected intervention duration: 3 months).
Arm Title
Wait-list/delayed intervention
Arm Type
Active Comparator
Arm Description
Participants randomized to the delayed intervention group will receive no intervention for 6 months post-randomization; after the 6-month follow-up period, the delayed intervention group also will participate in 3 video conferencing sessions with a CDCES interventionist and connect with a peer parent consultant (expected intervention duration: 3 months).
Intervention Type
Behavioral
Intervention Name(s)
diabetes education and parent coaching support
Intervention Description
Intervention sessions will include parent/child discussion about barriers to CGM use, review of CGM data, problem solving, and working as a team.
Primary Outcome Measure Information:
Title
Glycemic control
Description
hemoglobin A1c (HbA1c)
Time Frame
Baseline
Title
Glycemic control
Description
hemoglobin A1c (HbA1c)
Time Frame
3 months post randomization
Title
Glycemic control
Description
hemoglobin A1c (HbA1c)
Time Frame
6 months post randomization
Title
Glycemic control
Description
hemoglobin A1c (HbA1c)
Time Frame
12 months post randomization
Title
glycemic variability
Description
Using 14-30 days of CGM data
Time Frame
Baseline
Title
glycemic variability
Description
Using 14-30 days of CGM data
Time Frame
3 months post randomization
Title
glycemic variability
Description
Using 14-30 days of CGM data
Time Frame
6 months post randomization
Title
glycemic variability
Description
Using 14-30 days of CGM data
Time Frame
12 months post randomization
Secondary Outcome Measure Information:
Title
Family Conflict
Description
The Diabetes Family Conflict Scale-Revised Scored 19-57 where a higher score indicates higher family conflict
Time Frame
Baseline
Title
Family Conflict
Description
The Diabetes Family Conflict Scale-Revised Scored 19-57 where a higher score indicates higher family conflict
Time Frame
3 months post randomization
Title
Family Conflict
Description
The Diabetes Family Conflict Scale-Revised Scored 19-57 where a higher score indicates higher family conflict
Time Frame
6 months post randomization
Title
Family Conflict
Description
The Diabetes Family Conflict Scale-Revised Scored 19-57 where a higher score indicates higher family conflict
Time Frame
12 months post randomization
Title
Diabetes Distress
Description
Problem Areas in Diabetes scales (PAID) Scored 14-84 where higher scores indicate higher distress
Time Frame
Baseline
Title
Diabetes Distress
Description
Problem Areas in Diabetes scales (PAID) Scored 14-84 where higher scores indicate higher distress
Time Frame
3 months post randomization
Title
Diabetes Distress
Description
Problem Areas in Diabetes scales (PAID) Scored 14-84 where higher scores indicate higher distress
Time Frame
6 months post randomization
Title
Diabetes Distress
Description
Problem Areas in Diabetes scales (PAID) Scored 14-84 where higher scores indicate higher distress
Time Frame
12 months post randomization
Title
CGM benefits and burdens
Description
Continuous glucose monitoring (CGM) Burdens and Benefits as assessed by The BenCGM and BurCGM
Time Frame
Baseline
Title
CGM benefits and burdens
Description
Continuous glucose monitoring (CGM) Burdens and Benefits as assessed by The BenCGM and BurCGM
Time Frame
3 months post randomization
Title
CGM benefits and burdens
Description
Continuous glucose monitoring (CGM) Burdens and Benefits as assessed by The BenCGM and BurCGM
Time Frame
6 months post randomization
Title
CGM benefits and burdens
Description
Continuous glucose monitoring (CGM) Burdens and Benefits as assessed by The BenCGM and BurCGM
Time Frame
12 month post randomization
Title
CGM use
Description
Indicators of CGM use, including mean days work per week, will be evaluated to measure sustained use of CGM.
Time Frame
Baseline
Title
CGM use
Description
Indicators of CGM use, including mean days work per week, will be evaluated to measure sustained use of CGM.
Time Frame
3 months post randomization
Title
CGM use
Description
Indicators of CGM use, including mean days work per week, will be evaluated to measure sustained use of CGM.
Time Frame
6 months post randomization
Title
CGM use
Description
Indicators of CGM use, including mean days work per week, will be evaluated to measure sustained use of CGM.
Time Frame
12 months post randomization
Title
Diabetes self-management
Description
The Diabetes Management Questionnaire (DMQ)-a self- and parent-report measure assessing the frequency of engagement in diabetes care behaviors (e.g. BG monitoring, adjusting behavior to specific situations) over the past month. Scored 0-100 with higher scores indicating higher adherence to diabetes management
Time Frame
Baseline
Title
Diabetes self-management
Description
The Diabetes Management Questionnaire (DMQ)-a self- and parent-report measure assessing the frequency of engagement in diabetes care behaviors (e.g. BG monitoring, adjusting behavior to specific situations) over the past month. Scored 0-100 with higher scores indicating higher adherence to diabetes management
Time Frame
3 months post randomization
Title
Diabetes self-management
Description
The Diabetes Management Questionnaire (DMQ)-a self- and parent-report measure assessing the frequency of engagement in diabetes care behaviors (e.g. BG monitoring, adjusting behavior to specific situations) over the past month. Scored 0-100 with higher scores indicating higher adherence to diabetes management
Time Frame
6 months post randomization
Title
Diabetes self-management
Description
The Diabetes Management Questionnaire (DMQ)-a self- and parent-report measure assessing the frequency of engagement in diabetes care behaviors (e.g. BG monitoring, adjusting behavior to specific situations) over the past month. Scored 0-100 with higher scores indicating higher adherence to diabetes management
Time Frame
12 months post randomization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 10-15 years old Type 1 diabetes Type 1 diabetes diagnosis ≥ 6 months \ Starting a continuous glucose monitor for the first time or restarting after ≥ 1 year Exclusion Criteria: Younger than 10, older than 15 Diagnosed less than 6 months Already using CGM or has used within last year Other major medical condition such as cancer, cystic fibrosis
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Emma Straton
Phone
202-476-5360
Email
estraton@childrensnational.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Randi Streisand, PhD
Organizational Affiliation
Children's National Hosptial
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's National Research Institute
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20010
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Elena Gibson, MS
Phone
202-476-6877
Email
egibson@childrensnational.org
First Name & Middle Initial & Last Name & Degree
Randi Streisand, PhD

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Research on Optimizing the Use of Technology With Education

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