NCT07258758Recruiting
Diabetes Intervention Involving Person-centred Nutritional Education
Diabetes Intervention Involving Person-centred Nutritional Education (DINE) - Exploring the Benefits and Challenges of a Person-centred Education on the Nordic Diet for Adults With Type 1 Diabetes.
Source: ClinicalTrials.gov · Last updated 12 Dec 2025
Brief summary (registry, in English)
The overall objective for this project is to evaluate the effects of a person-centred education intervention to promote a healthy, sustainable Nordic diet compared with the current practice of providing short dietary information on health outcomes of adults with Type 1 diabetes. The study will measure the intervention's impact on blood glucose levels, blood lipids, blood pressure, and adherence to a sustainable and healthy Nordic diet. The main question the trial aims to answer is: Does a person-centred nutritional education have an impact on glucose time in range for adults with Type 1 diabetes, compared with short dietary information? The participants will: * Attend either a person-centred nutrition education (intervention) or receive short dietary information (control group). * Wear their sensor for continuous glucose monitoring (CGM) throughout the trial. * Visit the clinic for data collection (blood samples and clinical checks) at the start and end of the trial. * Keep a four-day food diary, fill out a food frequency questionnaire (FFQ) and estimate their food enjoyment at the start and end of the trial.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 54 (estimated)
- First submitted
- 20 Nov 2025
- Start date
- 1 Sept 2025
- Primary completion date
- 30 Jun 2027
- Lead sponsor
- Umeå University
- Diseases
- Type 1 diabetes
- NCT number
- NCT07258758
What you commit to
- Study type: Interventional
- Planned participants: 54
- From 1 Sept 2025 to the primary completion date, 30 Jun 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Current or planned treatment with corticosteroids during the study (other than for replacement therapy).
Other illness
- Cognitive impairment or other disease that study physician find non-compatible with participation.
- Food allergies or intolerances that are incompatible with adhering to Nordic nutrition recommendations.
Lab values
- Planned change in glucose lowering treatment during study period (change of mealtime insulin analogue with same pharmacodynamic profile allowed).
Other
- Women of childbearing potential: ongoing pregnancy or planned pregnancy during the study period.
- Planned change of CGM sensor during the study.
Who the study is looking for
- Type 1 Diabetes.
- Diabetes duration for more than 12 months at screening.
- Adults 18 years or older.
- HbA1c more than 57mmol/mol.
- Use of continuous glucose monitoring (CGM) sensor for more than three months at screening and during the study period.
- Use of basal and bolus insulin regimen for more than three months at screening and during the study period.
- Written Informed Consent.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Hospital of Enköping Coordinator of this site? Confirm its status | Enköping | Sweden | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.