Can meal timing help shift workers beat diabetes?
NCT ID NCT06912555
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at whether three different low-calorie diets could improve blood sugar and body composition in 120 shift workers who are overweight and have prediabetes or type 2 diabetes. Each diet had a different amount and timing of protein. The goal was to see which approach works best for people who work nights.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Low-calorie diet with different protein distributions
- What this could lead to
- If successful, this could show that adjusting when you eat protein helps shift workers better control blood sugar and lose fat.
- What could go wrong
- This is a small, completed study with only 120 participants. Results may not apply to all shift workers, and diet changes can be hard to stick with long-term.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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120 people
The number who actually took part.
- Started
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Sep 2024
- Finished
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Dec 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 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. Exclusion Criteria: * 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. * 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. * 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. * Use of medications that could interfere with lipid and/or glucose metabolism, unless taken stably throughout the study. * Consumption of sleep supplements, except for stable use for 6 months with the intention to continue stable use throughout the study. * Presence of any laboratory abnormalities that could affect study results. * Weight gain or loss of ≥ 5% in the last 3 months. * Use of vitamin supplements in an unstable manner for at least 6 months prior to study entry. * High intake of alcohol (\> 30 g of ethanol) on a regular basis. * Pregnancy or intention to become pregnant during the study. * 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. * 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.).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Instituto de Investigación Sanitaria Aragón, Hospital Universitario Miguel Servet, Universidad de Zaragoza
Zaragoza, Spain, 50009, Spain
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