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NCT03574103Recruiting

Chronic Effect of Fasting

Comparison of Weight Loss Induced by Daily Time-Restricted Feeding Versus Daily Caloric Restriction in Women With Overweight and Obesity

Source: ClinicalTrials.gov · Last updated 18 Mar 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The aim of the study is to determine if time-restricted feeding (TRF) is an effective dietary strategy to weight loss after 8 weeks intervention. TRF will be compared with an intervention without restriction in time for feeding. Both strategies will be with caloric restriction.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
45 (estimated)
First submitted
19 Jun 2018
Start date
9 Jul 2018
Primary completion date
Sept 2025
Lead sponsor
Federal University of Minas Gerais
Diseases
Obesity
NCT number
NCT03574103

What you commit to

  • Study type: Interventional
  • Planned participants: 45
  • From 9 Jul 2018 to the primary completion date, Sept 2025
  • 2 sites 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

  • Medications known to affect total energy expenditure;
  • Use of steroids, immunosuppressants or non-steroidal anti-inflammatory drugs, weight-loss medications, oral hypoglycemic agents or insulin and any medications that influence metabolic and/or inflammatory parameters;
  • Previous surgery for weight loss;

Other illness

  • Any chronic health conditions (e.g. chronic renal failure, autoimmune, heart, and liver disease);
  • Thyroid diseases or medications for its treatment;

Other

  • Pregnancy or breast-feeding;
  • Smoking;
  • Alcohol use (\>2 doses/day).

Who the study is looking for

  • Females;
  • Aged between 18 and 59 years old;
  • Body mass index equal or greater 25 kg/m²;
  • Agree to sign the informed consent.

Age in the registry: 18 years to 59 years · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

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

SiteCityCountrySite status
Hospital da Clínicas
Coordinator of this site? Confirm its status
Belo HorizonteBrazilRecruiting
Hospital das Clínicas
Coordinator of this site? Confirm its status
Belo HorizonteBrazilRecruiting

Related publications

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