Effectiveness of Individualized Automatic Coaching Message for Glycemic Management and Depressive… (NCT06769906) | Clinical Trial Compass
CompletedNot Applicable
Effectiveness of Individualized Automatic Coaching Message for Glycemic Management and Depressive Symptom
South Korea46 participantsStarted 2025-01-09
Plain-language summary
This is a 12-week, single-center, randomized, prospective, confirmatory study of effectiveness of the individualized automatic coaching messages for glycemic management based on continuous glucose monitoring and depressive symptom in insulin-treated patients with type 2 diabetes.
Who can participate
Age range
18 Years – 80 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:
* Patients for whom the use of a continuous glucose monitor has been determined based on the medical judgment of the attending physician.
* Insulin-treated type 2 diabetes patients, age 18-80 years old.
* Patients who have not changed their diabetes medication in the past 2 months.
* Patients with a glycated hemoglobin level between 6.5% and 12.0% within the last 3 months.
* Patients currently receiving insulin injection therapy, including basal insulin.
* Patients who have access to KakaoTalk via smartphone and are able to communicate with it.
* Voluntarily agreed to participate in this clinical study.
Exclusion Criteria:
* Steroid and immunosuppressant users. But it can be included if patients continuously maintain same drug dose at least three months.
* Patients who are currently taking weight control medications.
* Breastfeeding or pregnant patients
* Patients who do not voluntarily consent to the study
* Anyone deemed unsuitable by the investigator to participate in the study
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.