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Continuous Glucose Monitoring in Primary Care: Multidisciplinary Pilot Implementation Study
JMIR Diabetes 2025;10:e69061
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Nonliterate participants will document their informed consent by marking their ICF(s) (eg, with an X, thumbprint, or other mark) in the presence of a literate third-party witness. Participants will be provided with a copy of their ICF if they are willing to receive it.
All minors (under the age of 18) will be required to provide assent along with parental consent. According to Malawi guidelines, individuals aged 15 years and above may initiate Pr EP if they meet other eligibility criteria.
JMIR Res Protoc 2025;14:e72981
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The sample size was calculated based on the primary outcome of this study using G*Power 3.1.9.7 (Heinrich Heine University Düsseldorf) [25] and considering that the study design corresponds to a 3×2 factorial design (3 groups and 2 repeated measures). Therefore, we will determine the effect of treatment between the groups using a 2-way ANOVA and repeated measures.
JMIR Res Protoc 2025;14:e69131
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