Clinical Trials Directory

Trials / Recruiting

RecruitingNCT03574103

Chronic Effect of Fasting

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

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
45 (estimated)
Sponsor
Federal University of Minas Gerais · Academic / Other
Sex
Female
Age
18 Years – 59 Years
Healthy volunteers
Accepted

Summary

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.

Detailed description

The participants of the study will be divided in two groups: (1) a group with caloric restriction and without restriction in time for feeding and (2) a group with caloric restriction and restriction in time for feeding. This second group will be subdivided according to the participant's preference: (2.1) first meal at 8 a.m. and last meal at 4 p.m. or (2.2) first meal at 12 p.m. and last meal at 8 p.m. The caloric restriction for all participants will be 513 to 770 kcal from estimated energy requirement.

Conditions

Interventions

TypeNameDescription
BEHAVIORALCaloric restriction onlyParticipants in this group will receive a eating plan with caloric restriction (513 to 770 kcal from estimated energy requirements), without restriction in time for feeding, for 8 weeks.
BEHAVIORALCaloric restriction plus TRF morningParticipants in this group will receive a eating plan with caloric restriction (513 to 770 kcal from estimated energy requirements) and 8 hours for eating (from 12 p.m. to 8 p.m.) and 16 hours of fasting, for 8 weeks.
BEHAVIORALCaloric restriction plus TRF nightParticipants in this group will receive a eating plan with caloric restriction (513 to 770 kcal from estimated energy requirements) and 8 hours for eating (from 8 a.m. to 4 p.m.) and 16 hours of fasting, for 8 weeks.

Timeline

Start date
2018-07-09
Primary completion
2025-09-01
Completion
2026-12-01
First posted
2018-06-29
Last updated
2025-03-18

Locations

2 sites across 1 country: Brazil

Source: ClinicalTrials.gov record NCT03574103. Inclusion in this directory is not an endorsement.