Actively 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
Led by Cedars-Sinai Medical Center · Updated on 2026-03-18
37
Participants Needed
1
Research Sites
65 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
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
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 18 or older
- Diagnosed with Type 1 or Type 2 Diabetes and currently on insulin
- Able to speak and understand English
- Scheduled to receive a standard inpatient diabetes education consultation
- Have not used a continuous glucose monitoring device in the six months before admission
- Own a smartphone
- Able to follow instructions and provide informed consent to participate
You will not qualify if you...
- Known pregnancy due to changes in glucose metabolism and skin sensitivity
- Non-English speakers because study materials and surveys are only validated in English and additional resources are not available
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Cedars-Sina Medical Center
Los Angeles, California, United States, 90048
Actively Recruiting
Research Team
M
Mathew P Monterola, Doctor of Nursing Practice
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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