Status:
NOT_YET_RECRUITING
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.
Lead Sponsor:
Cedars-Sinai Medical Center
Conditions:
Diabetes Mellitus
Eligibility:
All Genders
18+ years
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 o...
Eligibility Criteria
Inclusion
- 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
- 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.
Key Trial Info
Start Date :
May 20 2025
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
October 30 2025
Estimated Enrollment :
37 Patients enrolled
Trial Details
Trial ID
NCT06965803
Start Date
May 20 2025
End Date
October 30 2025
Last Update
May 11 2025
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