4.4 Article

Psychosocial Impact of the Insulin-Only iLet Bionic Pancreas for Adults, Youth, and Caregivers of Youth with Type 1 Diabetes

Journal

DIABETES TECHNOLOGY & THERAPEUTICS
Volume 25, Issue 10, Pages 705-717

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/dia.2023.0238

Keywords

Psychosocial; Patient-reported outcomes; Bionic pancreas; Automated insulin delivery; Type 1 diabetes

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This study evaluated the psychosocial impact and user experience of the insulin-only configuration of iLet bionic pancreas in individuals with type 1 diabetes. The results showed that adults experienced a reduction in diabetes-specific emotional distress and fear of hypoglycemia, as well as improved perceived well-being. Children and teenagers also demonstrated high acceptability and reduced burden with the system, but the improvements in psychosocial outcomes were less clear.
Objective: To evaluate the psychosocial impact and user experience for the insulin-only configuration of iLet bionic pancreas (BP) in persons 6-83 years years of age with type 1 diabetes.Research Design and Methods: In this multicenter, randomized controlled, 13-week trial, 275 adults (221 randomly assigned to the BP group and 54 to the standard of care [SC] group) and 165 youth and their caregivers (112 randomly assigned to the BP group and 53 to the SC group) completed psychosocial questionnaires at baseline, mid-study, and the end of the trial.Results: In all age groups, most participants would recommend using the BP, including those with previous experience using automated insulin delivery devices. Similarly, the vast majority of participants reported a high level of perceived benefits and a low number of perceived burdens. Adult participants reported significant decreases in the fear of hypoglycemia and in diabetes-specific emotional distress, as well as improvements in their perceived well-being.Conclusion: Findings demonstrate acceptability, reduced burden, and positive psychosocial outcomes for adults. Children and teenagers also report high acceptability and reduced burden, but less clear improvements in psychosocial outcomes.Clinical Trial Registration Number: NCT04200313.

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