Trials (May 2024)

Implementation research: a protocol for two three-arm pragmatic randomised controlled trials on continuous glucose monitoring devices in people with type 1 diabetes in South Africa and Kenya

  • Elena Marbán-Castro,
  • Lorrein Muhwava,
  • Yvonne Kamau,
  • Elvis Safary,
  • Paul Rheeder,
  • Maria Karsas,
  • Tanja Kemp,
  • Johanè Freitas,
  • Michelle Carrihill,
  • Joel Dave,
  • Daniel Katambo,
  • Joan Kimetto,
  • Razana Allie,
  • Kenya ACCEDE study group,
  • South Africa ACCEDE study group,
  • Joseph Ndungu,
  • Ntombi Sigwebela,
  • Dorcas Akach,
  • Sarah Girdwood,
  • Berra Erkosar,
  • Brooke E. Nichols,
  • Cathy Haldane,
  • Beatrice Vetter,
  • Sonjelle Shilton

DOI
https://doi.org/10.1186/s13063-024-08132-7
Journal volume & issue
Vol. 25, no. 1
pp. 1 – 13

Abstract

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Abstract Background Self-monitoring of glucose is an essential component of type 1 diabetes (T1D) management. In recent years, continuous glucose monitoring (CGM) has provided an alternative to daily fingerstick testing for the optimisation of insulin dosing and general glucose management in people with T1D. While studies have been conducted to evaluate the impact of CGM on clinical outcomes in the US, Europe and Australia, there are limited data available for low- and middle-income countries (LMICs) and further empirical evidence is needed to inform policy decision around their use in these countries. Methods This trial was designed as a pragmatic, parallel-group, open-label, multicentre, three-arm, randomised (1:1:1) controlled trial of continuous or periodic CGM device use versus standard of care in people with T1D in South Africa and Kenya. The primary objective of this trial will be to assess the impact of continuous or periodic CGM device use on glycaemic control as measured by change from baseline glycosylated haemoglobin (HbA1c). Additional assessments will include clinical outcomes (glucose variation, time in/below/above range), safety (adverse events, hospitalisations), quality of life (EQ-5D, T1D distress score, Glucose Monitoring Satisfaction Survey for T1D), and health economic measures (incremental cost-effectiveness ratios, quality adjusted life years). Discussion This trial aims to address the substantial evidence gap on the impact of CGM device use on clinical outcomes in LMICs, specifically South Africa and Kenya. The trial results will provide evidence to inform policy and treatment decisions in these countries. Trial registration NCT05944731 (Kenya), July 6, 2023; NCT05944718 (South Africa), July 13, 2023.

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