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Taking people in GermanyNo phase

Testing Early Versus Late Time-Restricted Eating for Blood Sugar in Prediabetes

Compares early and late daily eating windows in adults with prediabetes or type 2 diabetes.

Plain-language title generated from the registry record
Registry title: Precise Eating Time to Improve Glycemic Control and Cardiometabolic Health in Prediabetes and Diabetes

Key facts

Where
Nuthetal, GermanySee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 75 years old?

Source: NCT07171281, who can take part

Where in Germany

  • German Institute of Human Nutrition Potsdam-RehbrueckeNuthetal, GermanyTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
German Institute of Human Nutrition
Trial code
NCT07171281
Record updated
29 September 2026
Original description
The objective of this study is to investigate the impact of hypocaloric time-restricted eating (TRE) at different day times (early versus late TRE) on glucose metabolism and other cardiometabolic parameters in individuals with overweight and with normal, or impaired glucose metabolism (prediabetes and type 2 diabetes). In addition, the study aims to elucidate the molecular mechanisms underlying these effects.Read full original descriptionShow less

Precise Eating Time to Improve Glycemic Control and Cardiometabolic Health in Prediabetes and Diabetes: the GLYCOTIME Trial

The objective of this study is to investigate the impact of hypocaloric time-restricted eating (TRE) at different day times (early versus late TRE) on glucose metabolism and other cardiometabolic parameters in individuals with overweight and with normal, or impaired glucose metabolism (prediabetes and type 2 diabetes). In addition, the study aims to elucidate the molecular mechanisms underlying these effects.

Inclusion: Overweight or obesity (BMI 25-40 kg/m²); Healthy glucose metabolism (fasting glucose <100 mg/dl and glucose after 2 hours OGTT <140 mg/dl); OR impaired glucose metabolism (fasting glucose 100-125 mg/dl and/or glucose after 2 hours OGTT 140-199 mg/dl and/or HbA1c 5.7-6.4%); OR type 2 diabetes (according to existing medical diagnosis or fasting glucose >126 mg/dl and/or glucose after 2 hours OGTT >200 mg/dl and/or HbA1c ≥6.5%); Daily eating window ≥12 hours.

Exclusion: Traveling across more than one time zone within one month prior to the study; Treatment with insulin, sulfonylureas, and GLP-1 receptor agonists, steroid use (oral, cutaneous, or parenteral), regular intake of melatonin, anticoagulation treatment that cannot be paused; Eating disorders, food intolerance/allergy to ingredients in the diet product, vegan diet, practicing time-restricted eating; Severe chronic illnesses or other conditions that are incompatible with the planned intervention and examination program (e.g. type 1 diabetes, recent cardiovascular event, malabsorption, cancer in the last two years, etc.); Weight changes > 5% within past 3 months; Shift work; Pregnancy and breastfeeding; Extreme early and extreme late chronotypes.

ClinicalTrials.gov NCT07171281