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Type 1 diabetes (T1D) requires constant monitoring and management of blood glucose. Specific tasks conducted multiple times a day by individuals with T1D (or parents of youth with T1D) include checking blood glucose via fingerstick or continuous glucose monitor, calculating and administering insulin doses via injections or insulin pumps, possibly taking additional medications to regulate blood glucose, paying attention to dietary intake, carbohydrate counting and administering the appropriate amount of insulin needed with every meal and snack, and making decisions about engaging in physical activities.

Incomplete cognitive development prevents young people with T1D from always recognizing healthful choices or behaving in a way that promotes health and minimizes short- and long-term complications. Indeed, as children transition into adolescence, engagement in T1D self-management tasks often decreases and A1C increases. This pattern occurs despite significant advancements in diabetes technology, in part due to generally low uptake and use and inequities for people with low socioeconomic status and from racially and ethnically marginalized groups, particularly with the continuous glucose monitor. Given the many behavioral and psychosocial factors (e.g., cognitive development, family interactions, motivation, behavioral reinforcement) that are related to patterns of deterioration in T1D self-management and worsening glycemic outcomes during the adolescent years, mental health professionals are well-suited to help young people with T1D improve self-management behaviors as well as physical and psychological health outcomes.

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