🔎 Trials Near Me

Home › Metabolic Syndrome › NCT04893226

Circadian Rhythms in Postmenopausal Women

RecruitingHealthy volunteers welcome

Who can join

Ages 45 to 65 · Women · Healthy volunteers welcome

Full eligibility criteria
Inclusion Criteria:

* postmenopausal women
* age 45-65 years
* prediabetic or have at least 2 features of metabolic syndrome

Exclusion Criteria:

* on hormone therapy
* diabetes
* heart disease
* alcohol consumption of \>2 drinks per day
* significant circadian disruption
* having care-taking responsibilities that significantly affect sleep
* shift work or irregular lifestyle
* uncontrolled sleep apnea or other uncontrolled sleep disorder
* extreme early or late chronotypes
* significant psychiatric disorders
* taking ADHD medications
* diagnosed dysregulated eating behaviors
* smoking \>5 cigarettes/day or 30 pack-year history
* participating in formal weight loss program
* not weight stable

About the study

This is a randomized, parallel two-arm clinical trial design to study the efficacy of time-restricted feeding on metabolic risk in postmenopausal women, who may be particularly vulnerable to disruption of circadian eating rhythms and the associated metabolic dysfunction. It is hypothesized that time-restricted feeding will improve insulin sensitivity, glucose tolerance, body weight, and other metabolic parameters in metabolically-unhealthy postmenopausal women.

What is being tested

Sponsor: Julie Pendergast · Participants: 164 · Started: Oct 19, 2021

Contact the study team

Official record on ClinicalTrials.gov — NCT04893226

Locations in the U.S.

KentuckyUniversity of Kentucky, Lexington

Conditions

From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.