Purpose

The objective of this project is to develop a behavioral intervention that combines wearable continuous glucose monitoring (CGM) with smartphone feedback and educational video clips generated by artificial intelligence (AI) software to improve glycemic control among individuals with pre-diabetes. The goal is to prevent transition to type 2 diabetes.

Condition

Eligibility

Eligible Ages
Over 35 Years
Eligible Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • 35 years of age or older - Willingness to wear CGM sensor - Prediabetes by finger prick blood A1C% or fasting glucose - Centers for Disease Control and Prevention (CDC) prediabetes risk test score of 5 or higher or recent prediabetes diagnosis from physician

Exclusion Criteria

  • Diagnosed with any disorder that interferes with glucose - Influential medical disorder/event affecting ability to participate in study - Incompatible smartphone device not pairing with Dexcom G6 app - Currently pregnant - Previously participated in other Continuous Glucose Monitoring studies - Having a planned trip outside California in the following 2 months

Study Design

Phase
N/A
Study Type
Interventional
Allocation
N/A
Intervention Model
Sequential Assignment
Intervention Model Description
An AB sequential condition design with CGM automated continuous glucose recording with glucose level masked and unmasked phases.
Primary Purpose
Prevention
Masking
None (Open Label)
Masking Description
Participants are blinded to glucose values during Phase A. The CGM system generates automated records of glucose and does not require observation from an outcomes assessor. The investigator does not engage with participants and becomes aware of unmasking after trial is completed.

Arm Groups

ArmDescriptionAssigned Intervention
Other
Single Group
Participants wear a CGM on the back of the arm. During Phase A, glucose values are not visible to participants. During Phase B, glucose values are visible via the phone app.
  • Device: CGM
    The CGM sensor is worn on the back of the arm and glucose levels are recorded continuously but levels are not shown on the participant's phone app in phase A.

Recruiting Locations

Southern California Center for Latino Health SCCLH
Los Angeles, California 90031

More Details

Status
Recruiting
Sponsor
David S Black, PhD

Study Contact

David S Black, PhD MPH
3234428223
davidbla@usc.edu

Detailed Description

The primary objective of this new project is to enhance glycemic control in individuals with prediabetes and deter the progression to Type 2 Diabetes (T2D) within the LA County community. Our proposal involves conducting a Phase 0 intervention development study. This study will enlist a final sample of N=50 adults who speak English and/or Spanish, have non-clinical prediabetes, and test positive for prediabetes via a finger-prick A1c% screening. Participants will wear CGM devices for 20 days, with glucose data masked for the first 10 days and unmasked for the next 10 days. During the unmasked phase, participants will receive daily health education videos on their smartphones. The study will compare the duration of glucose excursions between the masked and unmasked phases to assess the impact of CGM feedback and health education on glucose regulation.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.