The psychosocial burdens of living with diabetes

Abstract

AbstractAimTo better understand the prevalence of self‐reported psychosocial burdens and the unmet needs identified by people with diabetes in relation to routine diabetes visits.MethodsAn English language, online survey was distributed via social media, key stakeholder networks, charity and advocacy groups to adults with type 1 diabetes or type 2 diabetes. Survey items were designed by members of the FDA RESCUE Collaborative Community Governing Committee prior to pilot testing with potential participants. Descriptive statistical analyses were conducted, as well as thematic analyses on free‐text responses using NVivo v14.ResultsFour hundred and seventy‐eight participants completed the survey: 373 (78%) had type 1 diabetes, 346 (73%) identified as a woman and 433 (91%) were white. Most participants had experienced self‐reported (rather than diagnosed) anxiety and depression (n = 323 and n = 313, respectively), as well as fear of low blood sugars (n = 294), low mood (n = 290) and diabetes‐related distress (n = 257). Sixty‐eight percent reported that diabetes had negatively affected self‐esteem, 62% reported the feelings of loneliness, but 93% reported that friends/family/work colleagues were supportive when needed. Two hundred and seventy‐two percent (57%) reported that their diabetes team had never raised the topic of mental health. The overwhelming majority stated that the best thing their diabetes team could do to help was to simply ask about mental well‐being, listen with empathy and without judgement, and practice skills to understand psychosocial issues in diabetes.ConclusionIntegrating psychosocial discussions and support within routine healthcare visits is crucial to improve outcomes for people with diabetes. Such a biopsychosocial model of healthcare has long been advocated by regulatory bodies.