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

Recruiting now

Conditions studied: Diabetes Mellitus

In brief

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.

Key facts

Study ID: NCT06965803
Run by: Cedars-Sinai Medical Center
People needed: 37
Starts: 2025-10-01
Expected to finish: 2026-12-30
Last updated by the study team: 2026-03-18

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

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

You may not qualify if…

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.

Where it is running

Cedars-Sina Medical Center — Los Angeles, California, United States (enrolling)

Full record on ClinicalTrials.gov

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