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Completed
NCT05756868
The Effect of Time-Restricted Feeding on Anthropometry, Biochemical Parameters, Diet Quality and Eating Behavior
Conditions: Fasting
Sex: Female
Ages: 19 Years – 65 Years
Healthy volunteers: 1
Phase: NA
Enrollment: 40
Sponsor: Eastern Mediterranean University
Location: Cyprus
Summary
The goal of this randomized controlled trial is to to determine the effects of time-restricted feeding intervention on body weight, body composition, biochemical parameters and eating behaviors in overweight female individuals.The main questions it aims to answer are:Does time-restricted feeding intervention reduce daily energy intake?Does time-restricted dietary intervention result in body weight and body fat loss?Does time-limited nutritional intervention lead to improvements in biochemical parameters?Does time-restricted feeding intervention improve eating behavior and eating awareness?Does time-restricted feeding intervention adversely affect diet quality?The participants in the intervention group will receive a time restricted feeding intervention (first meal at 10:00, last meal at 18:00) for 6 weeks.
Meals of the participants are planned as 8 hours of eating and 16 hours of fasting.Participants in the control group will not receive any dietary intervention.
Eligibility Criteria
Inclusion Criteria:19-65 age rangeFemaleBMI: 24.9-29.9 kg/m²Maintaining general activity and exercise habits during the study periodStable body weight (<4 kg weight loss or weight gain) for 6 months prior to the start of the studyExclusion Criteria:Those with chronic disease (diabetes, hypertension, cardiovascular disease, etc.)Drug usersUse of supplements that may affect blood lipid profile and blood sugar (omega-3 etc.)Pregnant womenPeople in the lactation periodMenopauseShift workersThose who follow a Time Restricted (16:8) nutrition program before the studyThose who have followed any particular diet before the studyThose who frequently apply different weight loss diet programs
Source: ClinicalTrials.gov (NCT05756868). StuddyBuddy aggregates publicly available trial information.