Skip to main navigation Skip to search Skip to main content

Towards the standardisation of adult person-reported outcome domains in diabetes research: A Consensus Statement development panel

  • Katharine Barnard-Kelly
  • , David Marrero
  • , Maartje de Wit
  • , Frans Pouwer
  • , Kamlesh Khunti
  • , Norbert Hermans
  • , Jessica S. Pierce
  • , Lori Laffel
  • , Richard I.G. Holt
  • , Tadej Battelino
  • , Diana Naranjo
  • , Jacqueline Fosbury
  • , Lawrence Fisher
  • , William Polonsky
  • , Jill Weissberg-Benchell
  • , Korey K. Hood
  • , Oliver Schnell
  • , Laurel H. Messer
  • , Thomas Danne
  • , Revital Nimri
  • Soren E. Skovlund, Julia K. Mader, Jennifer L. Sherr, Desmond Schatz, Simon O'Neill, Emma Doble, Marissa Town, Karin Lange, Carine de Beaufort, Linda Gonder-Frederick, Sarah S. Jaser, Alon Liberman, David Klonoff, Nuha A. ElSayed, Raveendhara R. Bannuru, Christopher G. Parkin, Frank Snoek
  • BHR Ltd
  • University of Arizona
  • Amsterdam UMC
  • University of Southern Denmark
  • Novo Nordisk Foundation
  • University of Leicester
  • Research Institute of the Diabetes Academy Mergentheim (FIDAM)
  • Joslin Diabetes Center
  • University of Southampton
  • University of Ljubljana
  • Stanford University
  • United Kingdom Council for Psychotherapy
  • University of California at San Francisco
  • Behavioral Diabetes Institute
  • Northwestern University
  • Forschergruppe Diabetes e. VMunich
  • University of Colorado Boulder
  • Tandem Diabetes Care
  • Diabetes-Center for Children and Adolescents
  • Schneider Childrens Medical Center Israel
  • Tel Aviv University
  • Pharmaceutical Product Development
  • Medical University of Graz
  • Yale University
  • University of Florida
  • American Diabetes Association
  • Diabetes UK
  • Cincinnati Children's Hospital Medical Center
  • Hannover Medical School
  • University of Luxembourg
  • University of Virginia
  • Vanderbilt University
  • Sutter Health
  • Harvard University
  • Vrije Universiteit Amsterdam

Research output: Contribution to journalReview articlepeer-review

21 Scopus citations

Abstract

Diabetes is unique among chronic diseases because clinical outcomes are intimately tied to how the person living with diabetes reacts to and implements treatment recommendations. It is further characterised by widespread social stigma, judgement and paternalism. This physical, social and psychological burden collectively influences self-management behaviours. It is widely recognised that the individual's perspective about the impact of trying to manage the disease and the burden that self-management confers must be addressed to achieve optimal health outcomes. Standardised, rigorous assessment of mental and behavioural health status, in interaction with physical health outcomes is crucial to aid understanding of person-reported outcomes (PROs). Whilst tempting to conceptualise PROs as an issue of perceived quality of life (QoL), in fact health-related QoL is multi-dimensional and covers indicators of physical or functional health status, psychological and social well-being. This complexity is illuminated by the large number of person reported outcome measures (PROMs) that have been developed across multiple psychosocial domains. Often measures are used inappropriately or because they have been used in the scientific literature rather than based on methodological or outcome assessment rigour. Given the broad nature of psychosocial functioning/mental health, it is important to broadly define PROs that are evaluated in the context of therapeutic interventions, real-life and observational studies. This report summarises the central themes and lessons derived in the assessment and use of PROMs amongst adults with diabetes. Effective assessment of PROMs routinely in clinical research is crucial to understanding the true impact of any intervention. Selecting appropriate measures, relevant to the specific factors of PROs important in the research study will provide valuable data alongside physical health data.

Original languageEnglish
Article numbere15332
Pages (from-to)e15332
JournalDiabetic Medicine
Volume41
Issue number8
DOIs
StatePublished - Aug 2024

Keywords

  • Adult
  • Consensus
  • Diabetes Mellitus/therapy
  • Health Status
  • Humans
  • Patient Reported Outcome Measures
  • Quality of Life

Fingerprint

Dive into the research topics of 'Towards the standardisation of adult person-reported outcome domains in diabetes research: A Consensus Statement development panel'. Together they form a unique fingerprint.

Cite this