Continuous Glucose Monitoring for Self-Management of Type 2 Diabetes in Young Adults
CAPAZ-2D
CAPAZ-2D: Continuous Glucose Monitoring to Augment and Personalize Self-Management of Type 2 Diabetes in Hispanic/Latinx Young Adults
1 other identifier
interventional
40
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Oct 2025
Shorter than P25 for not_applicable
1 active site
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
First Submitted
Initial submission to the registry
June 5, 2025
CompletedFirst Posted
Study publicly available on registry
July 15, 2025
CompletedStudy Start
First participant enrolled
October 2, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 30, 2026
January 8, 2026
January 1, 2026
9 months
June 5, 2025
January 7, 2026
Conditions
Keywords
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
EXPERIMENTALParticipants 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.
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.
Eligibility Criteria
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
- San Diego State Universitylead
- Scripps Healthcollaborator
Study Sites (1)
Scripps Health
San Diego, California, 92121, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jessica L McCurley, PhD MPH
San Diego State University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- 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.