Improving Health Communication During the Transition From Pediatric to Adult Diabetes Care

Completed · Not applicable

Conditions studied: Type 1 Diabetes Mellitus

In brief

Adolescents and young adults (AYAs; ages 17-23) with type 1 diabetes are at high risk for negative health outcomes, including poor glycemic control and disengagement from the health care system. The deterioration of glycemic control occurs in parallel with the assumption of independent self-care skills and preparation for adult diabetes care. Effective communication between AYAs and health care providers may be a critical contributor to diabetes self-care skills during the transition to adult diabetes care and related glycemic control. This research will attempt to better prepare adolescents and young adults for adult diabetes care by delivering innovative intervention content focused on both health communication skills and transition readiness skills. The investigators aim to leverage innovative technologies to improve developmentally-appropriate communication skills related to planning for clinic visits, disclosing and discussing diabetes-related concerns, and optimizing glucose data review in preparation for adult diabetes care. Adolescents and young adults with type 1 diabetes (ages 17-23) who are planning to transition to adult diabetes care within the next 6-8 months will be enrolled in the study and randomized to either the intervention group or a standard care control group. Medical, communication and psychosocial data (including A1c, glucose monitoring frequency, communication quality, health care engagement, depressive symptoms) will be collected from adolescent and young adult participants and health care providers at baseline and two follow-up time points, approximately 4 months post-baseline and approximately 8-12 months post-baseline after the transfer to adult diabetes care. This intervention has the potential to improve diabetes self-care skills, including engagement with health care providers, and glycemic control in AYAs with type 1 diabetes during the vulnerable period of transfer to adult diabetes care. The results of this work will inform best practices for the transition to adult diabetes care and can be translated into clinical care.

Key facts

Study ID

NCT03734107

Run by

Children's National Research Institute

People needed

52

Starts

2018-11-06

Expected to finish

2026-01-02

Last updated by the study team

2026-05-26

Who can join

Age: 17 and older, up to 23. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Diagnosed with type1 diabetes for ≥ 1 year
• Able to adequately understand, speak, and read English to benefit from participation
• Ready and consistent text messaging access to participate
• Within 6-8 months of planned transfer to adult diabetes care

You may not qualify if…

• Other life-threatening disease (e.g. cancer) or major psychiatric disorder (e.g. schizophrenia) that significantly limits participation
• Pervasive developmental disorder that significantly limits participation

Where it is running

• Children's National Health System — Washington D.C., District of Columbia, United States

Full record on ClinicalTrials.gov

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