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.
Description:
AVAILABILITY OF DATA AND MATERIALS :
The only individual with access to the full dataset during the conduction of the trial will be the statistician at FIND. At the end of the trial, site-specific data will be made available to the research teams at the trial sites.
Reasonable requests for the trial data from academic parties will be considered by the corresponding author, and data may be made available in line with the data-sharing policies of FIND.
