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Education and Glucose Monitoring with CGM for Diabetes

This study is looking at whether providing education and using a continuous glucose monitor (CGM) can improve how satisfied people with diabetes are with their glucose monitoring and their overall quality of life. You might be able to join if you are 18 or older, have Type 1 or Type 2 diabetes, use insulin, speak English, are scheduled for diabetes education in the hospital, haven't used a CGM in the last six months, and own a smartphone. The main goal is to see if your satisfaction with glucose monitoring improves after 15 days. The study is currently unclear on its recruitment status and aims to enroll 37 participants.

Study design
This is an observational study, meaning researchers will watch and collect information without giving specific treatments. It plans to include 37 participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Your satisfaction will be measured at 15 days after starting the study.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06965803

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
Not specifiedAges 18+Observational
Cedars-Sinai Medical Center
~37 participants
Updated 2026-03-18 on ClinicalTrials.gov

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Patient Satisfaction (using a 5-point likert scale)
Measured over 15 days

Conditions

Diabetes Mellitus

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Where it's being run

1 sites across 1 states
California1

Who to contact

Mathew P Monterola, Doctor of Nursing Practice
[email protected]
3109677434
Email the study team

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Do you actually qualify for this trial?

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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.

What this trial measures

  • Patient Satisfaction (using a 5-point likert scale)15 days

    Glucose Monitoring Satisfaction Survey