Diabetes Mellitus, Type 1 Clinical Trial
Official title:
Type 1 Together: A Peer Mentorship Program to Increase Equitable Use of Continuous Glucose Monitoring Systems
Verified date | April 2024 |
Source | Nemours Children's Clinic |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The goal of this clinical trial is to evaluate a new way of helping adolescents with type 1 diabetes consistently use continuous glucose monitoring systems (CGM). Families who participate will be assigned by chance to one of two groups. One group will continue to see their Endocrinology provider who can give recommendations on ways to use CGM. The other group will be in our Type 1 Together program for 6 months. This will include: 1. Monthly meetings with a community health worker with expertise in type 1 diabetes self-management, 2. Access to CGM-specific educational resources hosted on a mobile app, and 3. Meeting at least monthly with a mentor family who will provide mentorship on using CGM consistently. The main questions the study aims to answer are: 1. Do families like the Type 1 Together program? 2. Do more families in the Type 1 Together program have better attitudes towards CGM, use CGM more consistently, and have lower HbA1c? 3. Does the Type 1 Together program reduce racial and ethnic differences in attitudes towards CGM, consistent use of CGM, and HbA1c?
Status | Enrolling by invitation |
Enrollment | 106 |
Est. completion date | February 28, 2027 |
Est. primary completion date | July 31, 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 12 Years to 17 Years |
Eligibility | Inclusion Criteria: - 12 to 17 years old - Diagnosed with type 1 diabetes for at least 6 months - Does not use CGM OR uses CGM < 24 out of the past 30 days - Able to read and write in English Exclusion Criteria: - Type 1 diabetes due to other medical condition (e.g., cystic fibrosis) - Intellectual disability - Severe psychiatric comorbidities |
Country | Name | City | State |
---|---|---|---|
United States | Nemours Children's Hospital, Delaware | Wilmington | Delaware |
Lead Sponsor | Collaborator |
---|---|
Nemours Children's Clinic | National Institute of General Medical Sciences (NIGMS) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Intervention Acceptability | How acceptable youth and caregivers find Type 1 Together. This information will be collected only from participants in the experimental arm using the Acceptability of Intervention Measure (scores range 1-5 with higher scores indicating greater acceptability). | 6 months post-enrollment | |
Primary | Perceptions of continuous glucose monitoring systems | Youth perceptions of the benefits and burdens of using continuous glucose monitoring systems will be assessed using the CGM Benefits and Burdens Scales (scores range 1-5 with higher scores indicating greater perceived benefits or burdens). | Baseline and 3, 6, 9, and 12 months post-enrollment. | |
Primary | Continuous Glucose Monitoring System Use | The number of days a patient wore their continuous glucose monitoring system at least 12 hours over the past month. | Baseline and 3, 6, 9, and 12 months post-enrollment | |
Primary | HbA1c | HbA1c expressed as a percentage of glycosylated hemoglobin | Baseline and 3, 6, 9, and 12 months post-enrollment |
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