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NCT06061042Recruiting

Effect of Timed-Restricted Eating on Metabolic Health

The Effect of Timed-Restricted Eating on Insulin Sensitivity, De Novo Lipogenesis and Liver Fat in Subjects With Obesity and Insulin Resistance

Source: ClinicalTrials.gov · Last updated 29 Sept 2023 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

We aim to determine the effect of combined isocaloric time restricted eating and meal timing on metabolic health, liver fat, functional brain networks, inflammation, and sleep pattern/quality in subjects with obesity and insulin resistance.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
30 (estimated)
First submitted
24 Sept 2023
Start date
Oct 2023
Primary completion date
Dec 2027
Lead sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
NCT number
NCT06061042

What you commit to

  • Study type: Interventional
  • Planned participants: 30
  • From Oct 2023 to the primary completion date, Dec 2027
  • 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

  • Drugs abuse or alcohol abuse (\>3 units/day);

Other illness

  • Use of any medication, except for those related to treatment of metabolic syndrome;
  • Any medical condition interfering with study outcomes or design;
  • History of any psychiatric disorder, including eating disorders;
  • Known soy, egg, milk or peanut allergy;

Other

  • Performing shift work
  • Performing intensive sports (\>3 hours/week);
  • Smoking;
  • Contraindication for MRI;
  • Known lactose/gluten intolerance;
  • Childhood onset of obesity

Who the study is looking for

  • Ability to provide informed consent;
  • BMI \> 30kg/m\^2;
  • Insulin resistance, as defined by fasting plasma insulin \> 62 pmol/L and/or prediabetes, as defined by fasting plasma glucose \> 5.3 and \< 7.0 mmol/L;
  • Stable weight for 3 months prior to study inclusion
  • For women, 1 year after last menstrual cycle

Age in the registry: 50 years to 75 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Amsterdam UMC, location AMC
Coordinator of this site? Confirm its status
AmsterdamNetherlandsRecruiting

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