Co-designing Enhanced Models of Care for First Nations Children at Risk for Childhood-onset Type … (NCT07692321) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Co-designing Enhanced Models of Care for First Nations Children at Risk for Childhood-onset Type 2 Diabetes
Canada600 participantsStarted 2026-08-31
Plain-language summary
The overall objective: to co-design and implement targeted and timely community led strategies to improve the health of the Next Generation and end the intergenerational impact of T2D in this population.
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 for the breastfeeding program:
* Pregnant women with type 2 diabetes or no diabetes.
* From self-identified Indigenous heritage (e.g., Cree, Oji-Cree, Métis, Anishinaabe, etc.) residing in the four Anisininew communities in the Island Lake region.
* Are delivering in Manitoba.
* Mother/Father and children must be biological family members.
Exclusion Criteria from the breastfeeding program:
* Parents or children with type 1 diabetes.
* Residing outside of Manitoba.
Inclusion criteria for the CGM pro
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
Proportion of mothers who initiate breastfeeding
Timeframe: 3 years
2
Number of eligible children in the NextGen Cohort screened per community
Timeframe: 3 years
3
Percentage of sensor time with glucose > 7.8 mmol/L
Timeframe: 3 years
4
Number of times the land-based wellness program ran
Timeframe: 3 years
5
Number of children who attend the land-based wellness programming
Timeframe: 3 years
6
Number of young adult leaders hired for the land-based wellness program