Technology Knowledge Optimization for Type 1 Diabetes in Schools (NCT07482488) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Technology Knowledge Optimization for Type 1 Diabetes in Schools
United States86 participantsStarted 2027-02
Plain-language summary
The goal of this study is to evaluate the feasibility and acceptability of a school nurse focused e-Learning application to improve their diabetes device knowledge and confidence. School nurses will be asked to complete pre-/post-surveys around a 16-week curriculum.
Who can participate
Age range
5 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 (School Nurses):
* Certified school nurse or obtaining certification
* Actively managing at least 1 student with type 1 diabetes ≤14 years of age who uses a diabetes device (CGM, insulin pump, or automated insulin delivery system)
* Employed in a school district in PA
* Equipped with a smartphone or device compatible with the app used to deliver curriculum
Inclusion Criteria (Parent-Child Dyads)
* Parent of a child diagnosed with T1D for ≥6 months
* Child ≤14 years of age and attends in-person school in Pennsylvania
* Child uses a CGM and/or AID system
Exclusion Criteria:
* Not able to participate in English (all)
* For School Nurses: No current work with in-person students (e.g., retired, cyber school only), not clinical school staff, prior participation 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.
What they're measuring
1
Study Enrollment
Timeframe: Baseline
2
Curriculum completion
Timeframe: Primary endpoint (completion of 16 week curriculum)
3
Retention
Timeframe: Primary endpoint (completion of 16 week curriculum)
4
Feasibility of Intervention Measure
Timeframe: Primary endpoint (completion of 16 week curriculum)
5
Acceptability
Timeframe: Primary endpoint (completion of 16 week curriculum)