Fact CheckerSign in

NCT06912555Completed

Effect of Low-calorie Diets With Different Macronutrient Composition and Macronutrient Distribution in Shift Workers With Prediabetes or Type 2 Diabetes and Overweight or Obesity.

A Randomized Study to Investigate the Effect of Low-calorie Diets With Different Macronutrient Composition and Macronutrient Distribution in Shift Workers With Prediabetes or Type 2 Diabetes and Overweight or Obesity.

Source: ClinicalTrials.gov · Last updated 11 May 2026

Brief summary (registry, in English)

Background and Aims: Shift work, particularly involving night shifts, is associated with increased risk of metabolic disturbances such as type 2 diabetes mellitus (T2DM). Thus, it is important to explore mechanisms underlying this deleteroius effect and strategies that could prevent or mitigate it. The aim of the study is to investigate the effect of three low-calorie diets with different macronutrients composition and distribution along day on glucose metabolism and other health outcomes in overweight or obese shift workers with prediabetes or T2DM. Methods: In this randomized controlled trial, 120 shift workers with a BMI \> 27.5 kg/m2 and diagnosed with prediabetes or T2DM will be recruited. The trial assesses three low-calorie diets effects on glucose metabolism, body composition, and health outcomes over 12 weeks. These diets include: A) high-protein dinner (60% of total daily protein), B) low-protein dinner (15% of total daily protein), and C) normoproteic diet.

Status (registry)
Completed
Study type
Interventional
Enrollment
120 (actual)
First submitted
24 Mar 2025
Start date
1 Sept 2024
Primary completion date
31 Aug 2025
Lead sponsor
Universidad de Zaragoza
NCT number
NCT06912555

What you commit to

  • Study type: Interventional
  • Participants enrolled: 120
  • From 1 Sept 2024 to the primary completion date, 31 Aug 2025
  • 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

  • Treatment with antidiabetic medications (oral or subcutaneous) or insulin in the last 2 months, except for stable use of metformin or Dipeptidyl peptidase 4 (DPP-4) inhibitors for a minimum of 6 months.
  • Treatment with lipid-lowering agents in an unstable manner for at least 6 months prior to study entry.
  • Use of vitamin supplements in an unstable manner for at least 6 months prior to study entry.

Other illness

  • Presence of other chronic conditions that are not well-controlled and could interfere with study outcomes, such as cardiovascular disease, renal disease, or liver disease.
  • Presence of uncontrolled endocrine disorders, including hypothyroidism.
  • Severe illness of any kind with a life expectancy of less than 1 year or that, in the investigators' judgment, limits uniform dietary intake throughout the study.

Lab values

  • Regular consumption of functional foods such as phytosterols or red yeast rice, which have a significant effect on lipid or glucose metabolism, in an unstable manner for at least 6 months prior to study entry.
  • Use of medications that could interfere with lipid and/or glucose metabolism, unless taken stably throughout the study.
  • Presence of any laboratory abnormalities that could affect study results.

Other

  • Consumption of sleep supplements, except for stable use for 6 months with the intention to continue stable use throughout the study.
  • Weight gain or loss of ≥ 5% in the last 3 months.
  • High intake of alcohol (\> 30 g of ethanol) on a regular basis.
  • Pregnancy or intention to become pregnant during the study.
  • Any other circumstance that, in the investigators' judgment, would impede adequate adherence to the proposed nutritional intervention (e.g., frequent travel during the study, inability to attend visits due to personal or work-related circumstances, etc.).

Who the study is looking for

  • Body mass index (BMI) ranging between 27.5 and 40 kg/m2.
  • Presence of prediabetes (fasting glucose between 100-125 mg/dL and/or glycated hemoglobin between 5.7 and 6.4%) or type 2 diabetes mellitus (fasting glucose ≥ 126 mg/dL and/or glycated hemoglobin ≥ 6.5% and/or currently taking metformin), based on the criteria of the American Diabetes Association.
  • Engaged in shift work, including night shifts, for at least 1 year and intending to maintain this schedule in the upcoming months.
  • Provide written informed consent for voluntary participation in the study after reviewing the participant information sheet and addressing any resulting queries.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Instituto de Investigación Sanitaria Aragón, Hospital Universitario Miguel Servet, Universidad de Zaragoza
Coordinator of this site? Confirm its status
ZaragozaSpainUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.