Enhancing Diabetes Management Approaches for Patients With Uncontrolled Diabetes (NCT05912647) | Clinical Trial Compass
RecruitingNot Applicable
Enhancing Diabetes Management Approaches for Patients With Uncontrolled Diabetes
United States376 participantsStarted 2024-02-03
Plain-language summary
The purpose of the study is to learn about the best way to enhance pharmacy-related care for diabetes self-management.
This research is being done because we want to improve use of medicines and diabetes management among adults with type 2 diabetes and find out which of type of support may improve diabetes self-management for adults.
Participants will be assigned to one of 4 groups, and will either:
* receive care as usual; or,
* receive added medicine management support from a pharmacist; or,
* receive support from a Community Health Worker (CHW) to address life challenges; or,
* receive both the pharmacist medicine management and the CHW support
Who can participate
Age range
18 Years – 90 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:
* Men and women ages 18-90 with diagnosed type 2 diabetes who speak and understand English or Spanish.
* Taking at least one oral or injectable diabetes medication
* HbA1c ≥ 7.5% based on point of care test.
* Will reside in the geographical area throughout the study period.
* Have access to a phone during the study period.
* Willing to attend all orientation/training sessions.
Exclusion Criteria:
* Having a caregiver who is the main decision maker in self-management.
* Participating in another lifestyle, or medication adherence program.
* Participated in standard MTM/MTM-related intervention in the last 6 months.
* Women who are pregnant or plan to get pregnant in the next 6 months.
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.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
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.