Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Diabetes Mellitus
  • Glucose Metabolism Disorders
  • Prediabetes
Design
Observational Model: CohortTime Perspective: Prospective

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

After being informed about the study and potential risks, all patients giving written informed consent wear a continuous glucose monitoring device ("iPro2" professional continuous glucose monitoring, Medtronic?, California, USA) and smart band ("Fitbit Inspire HR", Fitbit?, California, USA) for 1 we...

After being informed about the study and potential risks, all patients giving written informed consent wear a continuous glucose monitoring device ("iPro2" professional continuous glucose monitoring, Medtronic?, California, USA) and smart band ("Fitbit Inspire HR", Fitbit?, California, USA) for 1 week. During this period, all patients are tested oral glucose tolerance test and take a standard diet (calorie calculated) at morning. The patient's data from this study is compared to a predicted values by mathematical analysis model for diabetes prevention.

Tracking Information

NCT #
NCT04369833
Collaborators
Not Provided
Investigators
Principal Investigator: Sang soo Kim, Master Pusan National University Hospital