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Low Glycemic Index Diet in Patients With Type 1 Diabetes

Effects of a Low Glycemic Index Diet on HbA1c and Lipids in Patients With Type I Diabetes

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01184703
Acronym
LGID1
Enrollment
65
Registered
2010-08-19
Start date
2007-06-30
Completion date
2009-12-31
Last updated
2010-09-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Mellitus, Type 1

Keywords

Diabetes Mellitus, Type 1, Glycemic Index Diet, HbA1c, Lipids

Brief summary

The purpose of this study is to investigate if a low glycemic index diet in comparison with a medium/high glycemic index diet improves the metabolic control in patients with type 1 diabetes.

Detailed description

The glycemic index (GI) was introduced by Jenkins and co-workers in the early 1980s, and is a concept for ranking of carbohydrate foods based on their effect on postprandial glycaemia. A meta-analysis of randomised controlled trials of the effect of low GI diets in the management of diabetes showed a beneficial effect (i.e., a reduction in HbA1c) of low GI versus high GI foods. However, several critical points concerning the GI concept remain, for instance, how to apply it in practical every day life, how to calculate GI in mixed meals, how to find relevant low GI foods, how to ensure compliance to a low GI diet. The most important issue, however, is the fact that studies on the long-term effects of a low GI diet in type 1 diabetes are lacking. In this study, the critical issue of finding palatable low GI foods will be solved in close collaboration with the food industry. This may lead to the development of new commercial products with low GI, which is necessary if low GI diets are to be advocated for diabetics in the future. Comparison(s): A low glycemic index diet, compared to a medium/normal glycemic index diet.

Interventions

OTHERLow GI food

Comparison of carbohydrates in diabetic patients

Sponsors

Steno Diabetes Center Copenhagen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
20 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Type I diabetes, durability \>5 years * Age 20-65 years * Normal weight (BMI 19-26 kg/m2) * Diabetic treatment with mealtime and bedtime insulin. * HbA1c ≤10 % * Informed consent to participate in the study.

Exclusion criteria

* Diabetic complications; neuropathy, foot ulcers and/or gastroparesis. * A known food intolerance of gluten, leguminous plants, nuts or almonds. * Pregnancy or breast-feeding. * Concurrent participation in another research study with metabolic effects. * Previously regular follow-up with a dietician at SDC during the last year. * Adjustment during the study of medical treatment other than insulin and/or nutritional supplement with metabolic effects. * Non acceptance of the study diet or food products that are recommended in the study. * Disability to read and understand the Danish language. * Unable to receive and/or store the test products. * Place of residence \>1 hr drive from SDC.

Design outcomes

Primary

MeasureTime frame
HbA1c3 months

Secondary

MeasureTime frame
LDL-cholesterol3 months

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 9, 2026