NCT07065721

Brief Summary

Type 2 diabetes in increasing common in young adults. Utilizing a mixed-methods, community-based approach, this study offers continuous glucose monitors (CGMs) to young adults with type 2 diabetes for 30 days, and collects both quantitative and qualitative data to understand barriers and facilitators of CGM use, participants' changes in awareness of glucose patterns while using the CGM, and preferences for a CGM-based self-management intervention.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
3mo left

Started Oct 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress66%
Oct 2025Jul 2026

First Submitted

Initial submission to the registry

June 5, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

July 15, 2025

Completed
3 months until next milestone

Study Start

First participant enrolled

October 2, 2025

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

July 30, 2026

Last Updated

January 8, 2026

Status Verified

January 1, 2026

Enrollment Period

9 months

First QC Date

June 5, 2025

Last Update Submit

January 7, 2026

Conditions

Keywords

continuous glucose monitortype 2 diabetesyoung adult

Outcome Measures

Primary Outcomes (1)

  • Qualitative data regarding CGM use

    Semi-structured qualitative interviews will be conducted to understand barriers and facilitators of CGM use, changes in awareness of glucose patterns or relationships between glucose and health behaviors, and preferences for a future CGM-based intervention.

    Immediately after the intervention

Secondary Outcomes (1)

  • Acceptability and feasibility of CGM wear

    Immediately after the intervention

Other Outcomes (6)

  • Glucose time-in-range

    30 days (during the intervention period)

  • Diabetes self-care behaviors

    One week (7 days), last week of the intervention

  • Diabetes distress

    Baseline and follow-up (immediately after the intervention)

  • +3 more other outcomes

Study Arms (1)

CGM Wear

EXPERIMENTAL

Participants will wear a continuous glucose monitor for 30 days. They will also wear a FitBit activity tracker watch and complete weekly surveys to report diabetes self-management behaviors.

Device: Continuous glucose monitor

Interventions

Participants will wear a continuous glucose monitoring sensor for 30 days. They will also wear a FitBit wrist watch to be able to track their physical activity and they will complete weekly surveys to report diabetes self-management behaviors. After the 30 days, they will participate in a qualitative interview to respond to questions about their experiences.

CGM Wear

Eligibility Criteria

Age18 Years - 45 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • adult 18-45 years of age
  • diagnosis of type 2 diabetes in the last 5 years, as evidenced in the electronic medical record
  • no prior use or experience with wearable CGMs
  • possession of a smart phone that is compatible with Dexcom CGM sensors (nearly all smartphones are compatible) and willing to download and utilize the Dexcom CGM app
  • fluency in English or Spanish

You may not qualify if:

  • severe mental illness (e.g., psychosis, suicidal ideation);
  • pregnancy or \<6 months postpartum

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Scripps Health

San Diego, California, 92121, United States

RECRUITING

MeSH Terms

Conditions

Diabetes Mellitus, Type 2

Condition Hierarchy (Ancestors)

Diabetes MellitusGlucose Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesEndocrine System Diseases

Study Officials

  • Jessica L McCurley, PhD MPH

    San Diego State University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Jessica L McCurley, PhD, MPH

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Model Details: The intervention consists of a 30-day CGM wear and weekly surveys. Participants will be asked to maintain continuous use of CGM for 30 days and share their CGM data over that period. CGM sensors will be provided free-of-charge. Additionally, participants will be asked to complete weekly electronic surveys measuring self-management behaviors.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 5, 2025

First Posted

July 15, 2025

Study Start

October 2, 2025

Primary Completion (Estimated)

June 30, 2026

Study Completion (Estimated)

July 30, 2026

Last Updated

January 8, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Due to the very small size of this study, data will not be shared, as there is risk of identifying participants.

Locations