Clinical trial

Dietary Approaches for the Management of Overweight and Obesity in Type 1 Diabetes

Recruiting now · Not applicable · 1 countries · Registry ID NCT07667504

Recruiting nowNot applicableInterventional

What this study is about

Although type 1 diabetes (T1D) has traditionally been considered a disease associated with a lean phenotype, it is estimated that up to 2 out of 3 people living with T1D are overweight or obese, factors linked to an increased risk of complications in these patients. The available evidence regarding nutritional strategies for weight loss in T1D is very limited, and clinical trials are needed to determine how to effectively and safely promote weight loss in this population. In recent years, low-carbohydrate diets and several intermittent fasting protocols have demonstrated efficacy in promoting weight loss both in patients with type 2 diabetes and in patients with obesity without diabetes. This study will evaluate the efficacy of moderate carbohydrate restriction, time-restricted eating, and standard calorie restriction for weight loss in adults with T1D and overweight/obesity.

A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.

Basic eligibility

Age18 Years to 65 Years
SexAll
Healthy volunteersNot accepted
ConditionType 1 Diabetes (T1D), Obesity & Overweight

Full registry criteria

Inclusion Criteria: * T1D treated with intensive insulin therapy (multiple daily insulin injections or continuous subcutaneous insulin infusion systems) * HbA1c 6.5-9% * BMI ≥ 25 and ≤ 45 kg/m2 * Active prescription and use of CGM * Active prescription for glucagon Exclusion Criteria: * Pregnancy, pregnancy planning, or breastfeeding * Forms of diabetes other than T1D, or T1D duration \< 1 year * Previous cardiovascular events (acute myocardial infarction or stroke), heart failure, unstable coronary artery disease, chronic kidney disease with estimated glomerular filtration rate ≤ 30 mL/min/m², cirrhosis, or presence of active cancer * Unstable diabetes, episodes of glycemic decompensation (diabetic ketoacidosis) or severe hypoglycemia (level 3) within the past year. * Planned change in treatment during the study (switching from multiple daily insulin injections to continuous insulin infusion, or vice versa) * Use of sodium-glucose cotransporter 2 inhibitors, glucagon-like peptide-1 (GLP-1) receptor agonists, GLP-1/GIP agonists, or other medications that may influence weight loss * Having experienced a change in body weight greater than 5% within the 3 months before screening * Following any form of diet prior to inclusion, carbohydrate restriction, or intermittent fasting * History of eating disorders or alcohol abuse * Inability to follow the dietary recommendations * Presence of other conditions that, in the investigator's judgment, may compromise participation in the study.

Treatments and study arms

Moderate carbohydrate restriction

Behavioral

Participants will follow a diet with moderate carbohydrate restriction (25-30%), together with 25% caloric restriction

Early time-restricted eating

Behavioral

Participants will follow a standard diet with an 8-hour early eating window, starting no later than 10 a.m. (16-hour fast), together with 25% caloric restriction

Standard calorie restriction

Behavioral

Participants will follow a standard diet with 25% caloric restriction

Primary outcomes

Change in percent body weightFrom baseline to 6 months

Measured by a calibrated digital scale

Study locations

1 locations were listed when this page was built. The first 40 are shown.

Virgen de la Victoria University Hospital🇪🇸 Málaga, Málaga, Spain
José Ignacio Martínez-Montoro, MD, PhDPrincipal Investigator
Francisco J Tinahones, MD, PhDPrincipal Investigator