Clinical trial · NCT05858008 · RECRUITING · NA
Feasibility of Implementing Time-restricted Eating in Women With Mild Cognitive Impairment
Sponsor: Julie Pendergast
Summary
This study will investigate the feasibility of implementing a time-restricted eating intervention in females with mild cognitive impairment. Targeted therapeutic interventions that improve cognitive impairment and delay onset of ADRD are particularly important for females, who have twice the lifetime risk of developing AD, compared to males.
Interventions
- Time-restricted eating · BEHAVIORAL
Subjects will be educated about the health benefits of time-restricted eating. Each subject will self-select a 10-hour (10hr +/- 1 hr) window aligned with their active phase during which they will consume all daily calories. Subjects will text the time of their first and last daily calories for the duration of the study.
Published eligibility criteria
Verbatim from the registry. Only the site can decide how these apply to a specific patient.
Inclusion Criteria: * Postmenopausal Women * Age 45-95 * Diagnosis of mild cognitive impairment Exclusion Criteria: * Individuals prone to hypoglycemia * Liver disease * Taking medications that affect eating behaviors * Alcohol consumption of \>2 drinks per day * Significant circadian disruption * Having care-taking responsibilities that significantly affect sleep * Shift work or irregular lifestyle * Diagnosed clinical eating disorder * Participating in a formal weight loss program
Sites (1)
- University of Kentucky, Lexington, Kentucky · RECRUITING
Not medical advice. Trial0 is a navigation service, not a medical provider. Nothing here is medical advice or a recommendation to pursue any treatment; eligibility matching is informational, based on published registry criteria, and only the trial site or treating clinician can determine actual eligibility. Decisions belong with the patient and their own doctors. Registry data refreshed at most hourly; last update posted 2026-07-06.