Diabetes Prevention in Hispanic Adults Using Constant Glucose Monitors (NCT06864728) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Diabetes Prevention in Hispanic Adults Using Constant Glucose Monitors
United States30 participantsStarted 2025-01-28
Plain-language summary
The purpose of the study is twofold: to see the impact of your environmental stress on daily glucose changes and to create an intervention using CGM to potentially decrease risk for diabetes. The aim of this study to develop an intervention to prevent diabetes in the Hispanic community and inform policies about social determinants of health.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* self- identify as Hispanic Has a parent diagnosed with diabetes type 2
Exclusion Criteria:
* Pregnant Type 1 diabetes
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1This trial is focused on measuring 'diabetes knowledge' as its main outcome — does that mean it's primarily an education-based study rather than a medication or procedure trial, and how might that affect what I actually gain from participating?
2Since this study is specifically designed for Hispanic adults with prediabetes or type 2 diabetes and uses continuous glucose monitors, would wearing a glucose monitor full-time fit realistically into my daily routine, and is this approach something that could benefit me given my specific situation?
3The trial is listed as 'active, not recruiting,' which means they're no longer accepting new participants — does that close off this option for me entirely, or is there a similar study or program using continuous glucose monitors for diabetes prevention that you'd recommend I look into instead?
4Given that improving diabetes knowledge is the focus here, are there existing diabetes education programs or prediabetes prevention resources you'd suggest I pursue now, rather than waiting for results from a study like this one?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.