RecruitingNot ApplicableNCT07258758

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.


Sponsor

Umeå University

Enrollment

54 participants

Start Date

Sep 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests a person-centred nutrition education program for adults with type 1 diabetes whose blood sugar is not well controlled, to see whether personalized dietary guidance can improve glucose levels and overall diabetes management. **You may be eligible if...** - You have type 1 diabetes for more than 12 months - You are 18 or older - Your HbA1c (a 3-month blood sugar average) is above 57 mmol/mol (about 7.4%) - You have been using a continuous glucose monitor (CGM) and a basal-bolus insulin regimen for more than 3 months **You may NOT be eligible if...** - You are pregnant or planning pregnancy during the study - You have cognitive impairment or other conditions making participation difficult - You plan to change your glucose monitoring device or insulin regimen during the study - You have food allergies incompatible with Nordic dietary guidelines Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALDietary intervention

A person-centred education focussed on creating partnerships in care and shared decision-making.


Locations(1)

Hospital of Enköping

Enköping, Uppland, Sweden

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NCT07258758


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