Experiences of Caregivers and At-Risk Children Enrolled in a Prospective Pregnancy-Birth Cohort Study into the Causes of Type 1 Diabetes: The ENDIA Study

Author:

McGorm Kelly J.1ORCID,Brown James D.1,Roberts Alison G.23,Greenbank Susan4,Brasacchio Daniella4ORCID,Sawyer Alyssa C. P.5,Oakey Helena1ORCID,Colman Peter G.6ORCID,Craig Maria E.78,Davis Elizabeth A.23,Soldatos Georgia910,Thomson Rebecca L.1,Wentworth John M.611ORCID,Couper Jennifer J.112,Penno Megan A. S.1ORCID,

Affiliation:

1. Discipline of Paediatrics, Adelaide Medical School, Robinson Research Institute, The University of Adelaide, Adelaide, SA 5005, Australia

2. Rio Tinto Children’s Diabetes Centre, Telethon Kids Institute, University of Western Australia, Perth, WA 6009, Australia

3. Department of Endocrinology and Diabetes, Perth Children’s Hospital, Perth, WA 6009, Australia

4. Community and Consumer Involvement Group (CCIG), ENDIA Study, Adelaide, SA 5005, Australia

5. School of Psychology, The University of Adelaide, Adelaide, SA 5005, Australia

6. Diabetes and Endocrinology, Royal Melbourne Hospital, Melbourne, VIC 3050, Australia

7. The School of Women’s and Children’s Health, Faculty of Medicine, University of New South Wales, Sydney, NSW 2052, Australia

8. Institute of Endocrinology and Diabetes, The Children’s Hospital at Westmead, Sydney, NSW 2145, Australia

9. Monash Centre for Health Research and Implementation, School of Public Health and Preventive Medicine, Monash University, Melbourne, VIC 3004, Australia

10. Diabetes and Vascular Medicine Unit, Monash Health, Melbourne, VIC 3175, Australia

11. Walter and Eliza Hall Institute of Medical Research, Melbourne, VIC 3052, Australia

12. Diabetes and Endocrinology, Women’s and Children’s Hospital, North Adelaide, SA 5006, Australia

Abstract

Background: We sought research experiences of caregivers and their children were enrolled in the Environmental Determinants of Islet Autoimmunity (ENDIA) study. Methods: ENDIA is a pregnancy–birth cohort investigating early-life causes of type 1 diabetes (T1D). Surveys were sent to 1090 families between June 2021 and March 2022 with a median participation of >5 years. Caregivers completed a 12-item survey. Children ≥ 3 years completed a four-item survey. Results: The surveys were completed by 550/1090 families (50.5%) and 324/847 children (38.3%). The research experience was rated as either “excellent” or “good” by 95% of caregivers, and 81% of children were either “ok”, “happy” or “very happy”. The caregivers were motivated by contributing to research and monitoring their children for T1D. Relationships with the research staff influenced the experience. The children most liked virtual reality headsets, toys, and “helping”. Blood tests were least liked by the children and were the foremost reason that 23.4% of the caregivers considered withdrawing. The children valued gifts more than their caregivers. Only 5.9% of responses indicated dissatisfaction with some aspects of the protocol. The self-collection of samples in regional areas, or during the COVID-19 pandemic restrictions, were accepted. Conclusions: This evaluation identified modifiable protocol elements and was conducted to further improve satisfaction. What was important to the children was distinct from their caregivers.

Funder

JDRF Australia

The Leona M. and Harry B. Helmsley Charitable Trust

The National Health and Medical Research Council of Australia

Friends of the Women’s and Children’s Hospital

The Jack Newton Group

Publisher

MDPI AG

Subject

Pediatrics, Perinatology and Child Health

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