Making Diabetes Care Fit for Young Adults With Type 1 Diabetes

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study compares standard diabetes care with care that uses the Making Care Fit tool in encounters with young adults who have type 1 diabetes. Participants will have an observed clinical visit, a post-visit video-stimulated interview, and fill out questionnaires about their experience. The goal is to see if collaborative efforts to tailor care to daily life differ when the tool is used. The setting is Leiden University Medical Center and Diabeter in the Netherlands, and participants must be Dutch-speaking adults aged 18–30 with at least one year since diagnosis. The study design appears qualitative and observational in nature within a care-delivery context.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Young adults (age 18-30)
* with ≥1 year since the diagnosis of type 1 diabetes
* receiving ongoing treatment at participating diabetes clinics (Leiden university medical center (LUMC), Diabeter),
* able to speak and read Dutch
* able to provide informed consent for study participation

Exclusion Criteria:

* People who do not fit the participant requirements
* People who cannot give consent themselves (who are incapacitated)

Where it's running

• Leiden University Medical Center
  Leiden, South Holland, Netherlands Recruiting
• Diabeter
  Rotterdam, South Holland, Netherlands Recruiting

Study contacts

• Study coordinator: Marleen Kunneman, PhD
• Email: Kunneman@lumc.nl
• Phone: 0715263967

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• Semaglutide on body composition in adults with type 1 diabetes and overweight/obesity

  This study tests whether weekly semaglutide changes body composition in adults with type 1 diabetes who are overweight or obese, compared with a placebo over 24 weeks.

  Recruiting Phase 2/3 McGill University Health Centre/Research Institute of the McGill University Health Centre · Montreal, Quebec · NCT07891156

• Next Generation Extended Wear Sensors in Type 1 and Type 2 Diabetes

  This study tests a new extended wear sensor and algorithm in people with type 1 or type 2 diabetes to see how well it works across adults and children.

  Recruiting at 11 sites Medtronic MiniMed, Inc. · Chula Vista, California and 17 other locations · NCT07864168

• CGM-guided carb awareness education for adults with Type 1 diabetes

  This study tests whether teaching mealtime insulin dosing using CGM data helps adults with Type 1 diabetes who don’t usually count carbs.

  Recruiting University of California, Los Angeles · Los Angeles, California · NCT07807280

• Safety and effectiveness of GLP-1 receptor agonists and SGLT inhibitors added to insulin in adults with type 1 diabetes

  This registry will see if adding GLP-1RA or SGLTi therapies to insulin helps adults with type 1 diabetes over one year.

  Recruiting at 17 sites Indiana University · Newport Beach, California and 16 other locations · NCT07676565

• Think-Find-Solve activities for insulin self-management in children with type 1 diabetes

  A behavior-change activity book is tested with children aged 8–12 with type 1 diabetes and their parents to see if it improves daily insulin self-management.

  Recruiting Marmara University · Istanbul · NCT07670572

• Near-sensor insulin delivery with CGM in people with type 1 diabetes

  A small early-feasibility study tests a dual-port insulin patch pump that includes a CGM sensor to see if delivering insulin near the sensor affects glucose readings and whether an automated control algorithm can manage glucose.

  Recruiting Early Phase 1 ClinSurge Research · Toronto, Ontario · NCT07655076

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.