This Study is to Evaluate Whether Receiving Education and Glucose Monitoring With the CGM Device Will Improve Patient-reported Outcomes by Improving Patient's Satisfaction and Quality of Life (QOL) With Glucose Monitoring Device.
Not yet recruiting
- Conditions
- Diabetes Mellitus
- Registration Number
- NCT06965803
- Lead Sponsor
- Cedars-Sinai Medical Center
- Brief 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 37
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 English, enrolling non-English speakers would require additional resources/translations/personnel for evaluation and the education intervention that are not logistically possible right now.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Patient Satisfaction 15 days Glucose Monitoring Satisfaction Survey
- Secondary Outcome Measures
Name Time Method