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The Effect of Time-Restricted Eating in Cardiometabolic Health

The Effect of Time-Restricted Eating in Cardiometabolic Health

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04484987
Enrollment
55
Registered
2020-07-24
Start date
2020-11-20
Completion date
2024-05-20
Last updated
2024-08-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity, Pre-diabetes

Keywords

Chrono-nutrition, Adipose tissue, Skeletal muscle, Insulin sensitivity, Diurnal rhythm

Brief summary

Time-restricted eating (TRE) is a dietary manipulation that involves restricting food intake to 6-12 h/day with no energy intake the rest of the day. In rodents, TRE improves metabolic function without caloric restriction, potentially by activating nutrient sensing mechanisms and effects on circadian oscillations. However, an understanding of the effect of TRE on cardiometabolic health in people is not clear and few studies have evaluated this issue. Accordingly, the investigators propose to conduct a randomized controlled trial in people with obesity and prediabetes to determine the effect of 9 h TRE for 12 weeks, without a change in body weight, on key metabolic outcomes that are risk factors for cardiovascular disease (CVD): 1) multi-organ insulin sensitivity; 2) 24 h metabolic homeostasis and diurnal rhythm; and 3) adipose tissue and skeletal muscle biology. The proposed studies will elucidate the cardiometabolic implications of TRE in people with obesity and prediabetes.

Interventions

OTHER9 hours daily eating window

Participants assigned to the TRE group will have to consume all their daily meals and snacks during a 9-hour window for 12 weeks.

OTHER15 hours daily eating window

Participants assigned to the control group will have to consume all their daily meals and snacks during a 15-hour window for 12 weeks.

Sponsors

University of California, Davis
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Participants will be randomly assigned to one of two diet interventions: TRE group (eating all their food for the day in 9 hours) or the control group (eating all their food for the day in 15 hours) for 12 weeks. Tests to asses changes in metabolism will be performed before and after the intervention.

Eligibility

Sex/Gender
ALL
Age
21 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* body mass index 30-39.9 kg/m2 * fasting plasma glucose 100-125 mg/dl, or 2h OGTT plasma glucose 140-199 mg/dl or hemoglobin A1C 5.7-6.4% * self-reported habitual eating period \> 15 h per day

Exclusion criteria

* shift worker, recent or expected travel crossing time zones * fasting \>12 h/day more than once a week or vegan * shift worker, recent or expected travel crossing time zones * fasting \>12 h/day more than once a week or vegan * \> once a week no food intake after 1800 h * habitually waking up before 0400 h and sleeping before 2230 h * ≥ 150 min per week of structured exercise * unstable weight (\>5% change the last 2 months) * type 2 diabetes or other major chronic disease * sleep disorder * cancer in last 5 years * conditions that render subject unable to complete all testing procedures * use of medications that affect the study outcome measures or increase the risk of study procedures and that cannot be temporarily discontinued (e.g., steroids, alpha or beta adrenergic blockers or agonists, etc.) * smoking and illegal drug use * pregnant or lactating * menopause * individuals that have performed procedures involving substantial exposure to radiation in the last 12 months * gastrointestinal or bariatric surgery * unable to grant voluntary informed consent or comply with the study instructions * individuals who are not yet adults (infants, children, teenagers) * prisoners

Design outcomes

Primary

MeasureTime frameDescription
Insulin sensitivity3 months (pre-post intervention)Insulin sensitivity will be assessed by using a hyperinsulinemic euglycemic clamp procedure in conjunction with infusion of stable isotope tracers.
24 h glycemic control3 months (pre-post intervention)Changes in plasma glucose concentration will be assessed during a 24 h feeding study.
Adipose tissue gene expression3 months (pre-post intervention)Changes in the expression of genes involved in energy metabolism will be assessed by using qPCR.

Secondary

MeasureTime frameDescription
Peripheral diurnal rhythmicity in in peripheral mononuclear blood cells3 months (pre-post intervention)We will evaluate changes in clock gene expression

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026