About this trial
The purpose of the study is to improve patient-reported outcomes by improving patient's satisfaction and quality of life (QOL) with glucose monitoring device through pre and post satisfaction survey of patient with diabetes.
Eligibility criteria
Qualifiers
aged 18 or older
diagnosed with Type 1 or Type 2 Diabetes who are on insulin
able to speak and understand English language
scheduled to receive a standard inpatient diabetes education consultation
Disqualifiers
those who are known to be pregnant. This is due to complexity of pregnancy-related changes in glucose metabolism and increased skin sensitivity, or changes in skin condition to adhesives and materials used in CGM devices.
non-English speakers. As this is small study to evaluate which method is favorable using a survey only validated in English, enrolling non-English speakers would require additional resources/translations/personnel for evaluation and the education intervention that are not logistically possible right now.
Trial design
Treatments tested in this trial
- Not listed