NCT06965803

Recruiting

This Study is to Evaluate Whether Receiving Education and Gl...

Cedars-Sinai Medical Center Source

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Other study identifiers

Sponsor study identifier

STUDY00003936

Study Type

observational

Estimated enrollment

37

Locations

1 country

Sites

1

Timeline

Study Start

October 1, 2025

Actual (reported)

Primary Completion

December 30, 2026

Estimated

Planned date reported by the registry; this milestone is not confirmed as achieved.

Study Completion

December 30, 2026

Estimated

Planned date reported by the registry; this milestone is not confirmed as achieved.

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.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: recruiting
Estimated enrollment: 37 participants
Study completion date: December 30, 2026
Estimated
Planned date reported by the registry; this milestone is not confirmed as achieved.
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

First Submitted
May 2, 2025
Actual (reported)
First Posted
May 11, 2025
Actual (reported)
Study Start
October 1, 2025
Actual (reported)
Primary Completion
December 30, 2026
Estimated
Planned date reported by the registry; this milestone is not confirmed as achieved.
Study Completion
December 30, 2026
Estimated
Planned date reported by the registry; this milestone is not confirmed as achieved.

Last Updated: March 18, 2026
Status Verified: March 2026
Last Update Submitted: March 16, 2026

Conditions

Diabetes Mellitus

Outcome Measures

Primary Outcomes (1)

Patient Satisfaction (using a 5-point likert scale)
Glucose Monitoring Satisfaction Survey
15 days

Eligibility Criteria

Age18 Years+

Sexall

Healthy VolunteersNo

Age GroupsAdult (18-64), Older Adult (65+)

Sampling MethodNon-Probability Sample

Study Population

• Admitted patient with Type 1 or Type 2 diabetes.

You may qualify if:

aged 18 or older

Sponsors & Collaborators

Cedars-Sinai Medical Center
Otherlead

Study Sites (1)

Cedars-Sina Medical Center

Los Angeles, California, 90048, United States

RECRUITING

MeSH Terms

Conditions

Diabetes Mellitus

Condition Hierarchy (Ancestors)

Glucose Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesEndocrine System Diseases

Central Study Contacts

Mathew P Monterola, Doctor of Nursing Practice

CONTACT

3109677434 Mathew.Monterola@cshs.org

Study Design

Study Type: observational
Observational Model: COHORT
Time Perspective: PROSPECTIVE
Sponsor Type: OTHER
Responsible Party: PRINCIPAL INVESTIGATOR
PI Title: Associate Director, Clinical Support Programs

Study Record Dates

First Submitted

May 2, 2025

First Posted

May 11, 2025

Study Start

October 1, 2025

Actual (reported)

Primary Completion

December 30, 2026

Estimated

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Not ApplicableRecruiting

NCT07625254

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Not ApplicableCompleted

NCT05050019

DM DEVICE DISRUPTION SURVEY

Unknown

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.

Contact the study team to confirm eligibility.

Planned date reported by the registry; this milestone is not confirmed as achieved.

Study Completion

December 30, 2026

Estimated

Planned date reported by the registry; this milestone is not confirmed as achieved.

Last Updated

March 18, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing: Will not share

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT06965803
Data provider: ClinicalTrials.gov
Source updated: 2026-03-18
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:35:19 UTC

Locations

US(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

First Submitted

First Posted

Study Start

Primary Completion

Study Completion

Conditions

Outcome Measures

Primary Outcomes (1)

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Central Study Contacts

Study Design

Study Record Dates

You may not qualify if:

Data Sharing

Source record

Locations