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Do young people living with type-1 diabetes experience integrated care? The importance of integrating psychological support into interdisciplinary teams

Title: Do young people living with type-1 diabetes experience integrated care? The importance of integrating psychological support into interdisciplinary teams
Authors: Zurynski, Yvonne; Carrigan, Ann; Bebbington, Keely; Smith, Carolyn (K-lynn); Jones, Tim; Braithwaite, Jeffrey; Davis, Elizabeth
Source: International Journal of Integrated Care; Vol. 26 No. S1 (2026): 25th International Conference on Integrated Care, Lisbon, Portugal, 14-16 May 2025; 133 ; 1568-4156
Publisher Information: Ubiquity Press
Publication Year: 2026
Collection: International Journal of Integrated Care (IJIC)
Description: Introduction: Type 1 diabetes (T1D) is a chronic, incurable autoimmune condition, typically diagnosed in childhood and managed in paediatric services until ages 16–18 years, when young people (YP) transition to adult services. Maintaining tight glucose control and avoiding hypoglycaemia is challenging around this time as YP face psychosocial challenges and significant life-stage changes. International guidelines suggest that YP and their clinical teams need to prepare and plan for transition whilst building care continuity and supporting resilience and independence of YP to maintain glycaemic control during this vulnerable life-stage. Approach: We conducted a multi-methods study to understand the level of care continuity and integration at transition to adult services for Australian YP living with T1D. The study included a co-designed national survey of YP living with T1D across all states and territories of Australia undertaken in 2023, one-on-one interviews with 15 YP and a survey of service leaders. The surveys were developed in REDCap and made available online. YP were recruited via diabetes related organisations such as the Juvenile Diabetes Research Foundation, Diabetes Australia networks and the National Diabetes Services Scheme. Service leaders were recruited via clinical networks. Results: YP aged 14 – 25 years (n=226; 70M, 151F, 5 non-binary) from seven states and territories of Australia completed the survey. Approximately half (111, 49%) had transitioned to adult services and of these, only 21(23%) felt that they had been well prepared for transition, 9(8%) said transition had never been mentioned, and only 22(24%) had a written transition plan. Only 16(14%) met the adult team prior to transitioning. YP described lack of care integration when accessing adult care: "I just want a bit more certainty. I just want to know that every time I go to my appointment, I will have an appointment." (YP on accessing adult care in a regional city). YP had significant psychosocial complexity in addition to their ...
Document Type: article in journal/newspaper
File Description: application/pdf
Language: English
Relation: https://account.ijic.org/index.php/up-j-ijic/article/view/10442/11256
DOI: 10.5334/ijic.ICIC25133
Availability: https://account.ijic.org/index.php/up-j-ijic/article/view/10442; https://doi.org/10.5334/ijic.ICIC25133
Rights: Copyright (c) 2026 The Author(s) ; https://creativecommons.org/licenses/by/4.0
Accession Number: edsbas.247B3C26
Database: BASE