Clinical trial

Time Restricted Feeding, Muscle, and Metabolism

Recruiting now · Not applicable · 1 countries · Registry ID NCT04949451

Recruiting nowNot applicableInterventional

What this study is about

Effective nutrition strategies for combatting and/or preventing obesity still need to be identified. This has been the case despite the numerous and different approaches that have been taken. Potential targets for combatting/preventing obesity have been identified, but long-term solutions have not emerged. This study uses time restricted feeding to study the role of dietary protein in obesity prevention and/or treatment. The objectives are to determine the role of skeletal muscle mass as a driver of energy-sensing mechanisms and peripheral signals that regulate appetite and energy intake in overweight and obese adults and to determine the effects of protein timing on muscle mass to regulate appetite and energy intake in overweight and obese adults.

A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.

Basic eligibility

Age25 Years to 50 Years
SexAll
Healthy volunteersAccepted
ConditionOverweight, Obesity

Full registry criteria

Inclusion Criteria: * Resides in Northwest Arkansas * Age 25-50 years * BMI \> 25 * All ethnicities * Female and male Exclusion Criteria: * Food allergies * Pregnant or breastfeeding * Dietary restrictions (e.g. vegetarian, vegan, etc.) * Trying to lose weight in last 3 months * Pre-existing health conditions related to obesity (e.g. cardiovascular disease, diabetes, hypertension) * Prescription medications related to heart disease or type 2 diabetes * Fear of needles * Smoker or vaping * Currently taking protein supplements or other nutritional supplements which may interfere with study outcomes * Consumes \>4 alcoholic beverages per week

Treatments and study arms

Whey protein supplement

Dietary Supplement

Participants consume whey protein at the beginning of the eating period.

Ketogenic aid

Dietary Supplement

Participants consume ketogenic aid upon waking.

Control group - time restricted feeding only

Other

Time restricted feeding.

Primary outcomes

Body compositionChange is being assessed at baseline and final day (day 120) of the intervention.

Body composition measured using dual x-ray absorptiometry to determine the ration of lean/fat-free mass to fat mass.

Study locations

1 locations were listed when this page was built. The first 40 are shown.

University of Arkansas🇺🇸 Fayetteville, Arkansas, United States
Jamie I Baum, PhDContact