Feasibility and impact of an evidence-based electronic decision support system for diabetes care in family medicine: protocol for a cluster randomized controlled trial

HIGHLIGHTS

• who: Guideline implementation and colleagues from the Before the start of study, we will present the physicians with an informed consent that outlines the EBMeDS intervention and the purpose of the trial to study the effectiveness of the systemIndividual informed consent from the patient cannot be sought. Reminders show up unexpectedly during practice when patient data deviate from evidence-based targets. It is not practical to ask for informed consent at these moments. Furthermore, reminding the physician of the informed consent forms at every consultation may bias the study results in favor of the intervention. Data exports . . .
  

   

  

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