This Study is to Evaluate Whether Receiving Education and Glucose Monitoring With the CGM
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.
| Condition(s) | Diabetes Mellitus |
|---|---|
| Status | Recruiting |
| Study type | Observational |
| Summary | 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. |
| Who can participate | Inclusion Criteria: * 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 * must not have used CGM in the six months prior to admission * owns a smartphone * demonstrates the ability to follow instructions and be capable of providing informed consent to participate in the program Exclusion Criteria: * 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 Englis |
| Ages | 18 Years |
| Sex | All |
| Lead sponsor | Cedars-Sinai Medical Center |
| Locations | Los Angeles, California, United States |
| Start date | 2025-10-01 |
| NCT ID | NCT06965803 |
| Official listing | https://clinicaltrials.gov/study/NCT06965803 |