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Peer-reviewedCC BYFrontiers in clinical diabetes and healthcare

Acceptability of blinded continuous glucose monitoring for people with serious mental illness and type 2 diabetes: findings from an exploratory mixed-methods study.

5 affiliations
  1. 1School of Medicine and Population Health, University of Sheffield, Sheffield, United Kingdom.
  2. 2Department of Health Sciences, University of York, York, United Kingdom.
  3. 3Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds/Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
  4. 4Hull York Medical School, University of York, York, United Kingdom & Bradford District Care NHS Foundation Trust, Saltaire, United Kingdom.
  5. 5School of Nursing and Public Health, Manchester Metropolitan University, Manchester, United Kingdom.

Abstract

Introduction

People with serious mental illness (SMI) experience a disproportionately high prevalence of type 2 diabetes and a reduced life expectancy of 15 to 20 years. While continuous glucose monitoring (CGM) has revolutionised diabetes self-management in the general population, its feasibility and acceptability among individuals living with co-existing SMI remain largely unexamined.Methods

The study was embedded within the DIAMONDS feasibility study. Community-dwelling adults with SMI and type 2 diabetes (N = 21 eligible) were invited to wear a blinded CGM sensor (FreeStyle LibrePro) for 14 days. Quantitative metrics evaluated uptake, wear duration, data completeness, and adverse events. Semi-structured qualitative interviews (n = 9) explored user experiences. The qualitative analysis used a hybrid human-AI framework approach to map findings onto the Theoretical Framework of Acceptability (TFA) and the Theoretical Domains Framework (TDF), followed by data integration using a convergence coding matrix.Results

Sixteen participants agreed to wear the device (76.2% uptake), achieving a mean wear duration of 11 days. Of the returned sensors with data, 92.8% captured ≥5 days of readings, and no adverse events were reported. Qualitative analysis demonstrated highly positive affective attitudes and a significantly lower perceived burden compared with traditional finger-stick testing, despite minor challenges with sensor adhesion. Cross-framework integration revealed that high acceptability was driven by the device's low-friction physical layout, positive participant beliefs about data consequences, and alignment with a proactive, research-contributing identity.Discussion

The use of blinded CGM is both feasible and acceptable for people living with SMI and type 2 diabetes. These findings offer a robust foundation for developing structured, low-burden, and theory-informed physical health interventions aimed at closing the mortality gap in this underserved population.

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BibTeX
@article{brown2026acceptability,
  title = {{Acceptability of blinded continuous glucose monitoring for people with serious mental illness and type 2 diabetes: findings from an exploratory mixed-methods study.}},
  author = {Jennifer V E Brown and Ramzi A Ajjan and Najma Siddiqi and Peter A Coventry},
  journal = {Frontiers in clinical diabetes and healthcare},
  year = {2026},
  month = oct,
  doi = {10.3389/fcdhc.2026.1923186},
  url = {https://europepmc.org/article/MED/42909332},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Acceptability of blinded continuous glucose monitoring for people with serious mental illness and type 2 diabetes: findings from an exploratory mixed-methods study.
AU  - Jennifer V E Brown
AU  - Ramzi A Ajjan
AU  - Najma Siddiqi
AU  - Peter A Coventry
PY  - 2026
DA  - 2026/10/07
JO  - Frontiers in clinical diabetes and healthcare
DO  - 10.3389/fcdhc.2026.1923186
UR  - https://europepmc.org/article/MED/42909332
AB  - Introduction  People with serious mental illness (SMI) experience a disproportionately high prevalence of type 2 diabetes and a reduced life expectancy of 15 to 20 years. While continuous glucose monitoring (CGM) has revolutionised diabetes self-management in the general population, its feasibility and acceptability among individuals living with co-existing SMI remain largely unexamined.Methods  The study was embedded within the DIAMONDS feasibility study. Community-dwelling adults with SMI and type 2 diabetes (N = 21 eligible) were invited to wear a blinded CGM sensor (FreeStyle LibrePro) for 14 days. Quantitative metrics evaluated uptake, wear duration, data completeness, and adverse events. Semi-structured qualitative interviews (n = 9) explored user experiences. The qualitative analysis used a hybrid human-AI framework approach to map findings onto the Theoretical Framework of Acceptability (TFA) and the Theoretical Domains Framework (TDF), followed by data integration using a convergence coding matrix.Results  Sixteen participants agreed to wear the device (76.2% uptake), achieving a mean wear duration of 11 days. Of the returned sensors with data, 92.8% captured ≥5 days of readings, and no adverse events were reported. Qualitative analysis demonstrated highly positive affective attitudes and a significantly lower perceived burden compared with traditional finger-stick testing, despite minor challenges with sensor adhesion. Cross-framework integration revealed that high acceptability was driven by the device's low-friction physical layout, positive participant beliefs about data consequences, and alignment with a proactive, research-contributing identity.Discussion  The use of blinded CGM is both feasible and acceptable for people living with SMI and type 2 diabetes. These findings offer a robust foundation for developing structured, low-burden, and theory-informed physical health interventions aimed at closing the mortality gap in this underserved population.
SN  - 2673-6616
ER  -